Ireland
--:--IST
Recruiting Observational

iCaReMe Global Registry: Multinational Real-world Evidence in Cardiorenal and Metabolic Diseases

NCT03549754 · tracked via the Priya Life Science India tracker
Phase
Observational
Started
2018-02-17
Last updated
2026-09-09

Condition(s) studied

Type 2 DiabetesHypertensionChronic Kidney DiseaseHeart Failure

Study summary

To provide real world data on patient characteristics, disease management, healthcare utilization, and outcomes in patients with type 2 diabetes, Hypertension, Heart failure and/or Chronic kidney diseases

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Being 18 years or older 2. Having type 2 diabetes, Hypertension, Heart Failure and/or chronic kidney disease 3. Providing written informed consent to participate in the registry Exclusion Criteria: 1. Having a life-threatening co-morbidity with life expectancy below 1 year 2. Participating in an interventional trial requiring informed consent

Primary outcome measure(s)

  • 1. Age of particpants — At Baseline
    Age of participants at enrollment reported as mean ± standard deviation (SD) and median with interquartile range (IQR) in years.
  • 2. Percentage of Participants by Sex — At baseline
    Distribution of participants by sex (male/female) reported as counts and percentages.
  • 3. Percentage of Participants by Ethnicity — At Baseline
    Distribution of participants by ethnicity reported as counts and percentages for each ethnic category.
  • 4. Percentage of Participants by Education Level — At Baseline
    Distribution of participants by education level reported as counts and percentages for each education category.
  • 5. Percentage of Participants by Marital Status — At Baseline
    Distribution of participants by marital status reported as counts and percentages for each marital status category.
  • 6. Percentage of Participants with Family History of Cardiovascular and Renal-Metabolic Disease — At Baseline
    Percentage of participants with a family history of cardiovascular, renal, or metabolic (CVRM) disease (yes/no) reported as counts and percentages.
  • 7.Percentage of Participants by Physical Activity Level — At Baseline
    Distribution of participants by physical activity level category reported as counts and percentages.
  • 8. Percentage of Participants by Smoking Status — At Baseline
    Distribution of participants by smoking status (current smoker/former smoker/never smoked) reported as counts and percentages.
  • 9. Percentage of Participants by Alcohol Consumption — At Baseline
    Distribution of participants by alcohol consumption category reported as counts and percentages.
  • 10. Body Weight of Participants — At Baseline
    Body weight of participants reported as mean ± standard deviation (SD) and median with interquartile range (IQR) in kilograms (kg).
  • 11. Height of Participants — At Baseline
    Height of participants reported as mean ± standard deviation (SD) and median with interquartile range (IQR) in meters (m).
  • 12. Body Mass Index (BMI) of Participants — At Baseline
    Body mass index (BMI), calculated from weight and height, reported as mean ± standard deviation (SD) and median with interquartile range (IQR) in kg/m².
  • 13. Waist Circumference of Participants — At Baseline
    Waist circumference of participants reported as mean ± standard deviation (SD) and median with interquartile range (IQR) in centimeters (cm).
  • 14. Waist-to-Hip Ratio of Participants — At Baseline
    Waist-to-hip ratio of participants reported as mean ± standard deviation (SD) and median with interquartile range (IQR) (unitless ratio).
  • 15. Waist-to-Height Ratio of Participants — At Baseline
    Waist-to-height ratio of participants reported as mean ± standard deviation (SD) and median with interquartile range (IQR) (unitless ratio).
  • 16. Percentage of Participants by Cardiac and Renal Functional Measurements Category — At Baseline
    Distribution of participants by cardiac and renal functional measurement categories reported as counts and percentages.
  • 17. Primary Disease Duration — At Baseline
    Duration of primary disease (T2DM, HTN, HF, or CKD) from initial diagnosis to enrollment reported as mean ± standard deviation (SD) and median with interquartile range (IQR) in years.
  • 18. Percentage of Participants by Number and Types of Comorbidities — At Baseline
    Distribution of participants by number and types of comorbidities reported as counts and percentages for each comorbidity category.
  • 19. Percentage of Participants by NYHA Functional Class — At Baseline
    Distribution of heart failure participants by New York Heart Association (NYHA) functional class (I, II, III, IV) reported as counts and percentages.
  • 20. Percentage of Participants by Heart Failure Phenotype — At Baseline
    Distribution of heart failure participants by phenotype (HFrEF: ejection fraction ≤40%, HFmrEF: 41-49%, HFpEF: ≥50%) reported as counts and percentages.
  • 21. Percentage of Participants by Heart Failure Etiology — At Baseline
    Distribution of heart failure participants by etiology (ischemic, non-ischemic, valvular, hypertensive, other) reported as counts and percentages.
  • 22. Percentage of Participants by CKD Etiology — At Baseline
    Distribution of chronic kidney disease participants by etiology (diabetic nephropathy, hypertensive nephrosclerosis, glomerulonephritis, other) reported as counts and percentages.
  • 23. Percentage of Participants by Hypertension Stage — At Baseline
    Distribution of hypertension participants by stage (Stage 1, Stage 2, Stage 3) reported as counts and percentages.
  • 24. Percentage of Participants by Secondary Hypertension Etiology — At Baseline
    Distribution of participants with secondary hypertension by etiology reported as counts and percentages for each etiology category.
  • 25. Office Systolic and Diastolic Blood Pressure — At Baseline
    Office blood pressure reported as mean systolic blood pressure ± standard deviation (SD) and mean diastolic blood pressure ± SD in mmHg.
  • 26. Home Blood Pressure Monitoring (HBPM) Systolic and Diastolic Values — At Baseline
    Home blood pressure monitoring (HBPM) values reported as mean systolic blood pressure ± standard deviation (SD) and mean diastolic blood pressure ± SD in mmHg.
  • 27. Ambulatory Blood Pressure Monitoring (ABPM) Systolic and Diastolic Values — At Baseline
    Ambulatory blood pressure monitoring (ABPM) values reported as mean systolic blood pressure ± standard deviation (SD) and mean diastolic blood pressure ± SD in mmHg.
  • 28. Blood HbA1c — Average of 3 years
    HbA1c values reported as mean ± standard deviation (SD) and median with interquartile range (IQR) in %
  • 29. Fasting Glucose — Average of 3 years
    Fasting Glucose reported as mean ± standard deviation (SD) and median with interquartile range (IQR) in mg/dL
  • 30. Lipid Profile Testing — Average of 3 years
    Total cholesterol, LDL-C, HDL-C, triglycerides reported as mean ± standard deviation (SD) and median with interquartile range (IQR) in mg/dL
  • 31. Serum Creatinine — Average of 3 years
    Serum creatinine value reported as mean ± standard deviation (SD) and median with interquartile range (IQR) in mg/dL.
  • 32. Estimated Glomerular Filtration Rate (eGFR) — Average of 3 years
    Estimated glomerular filtration rate (eGFR) reported as mean ± standard deviation (SD) and median with interquartile range (IQR) in mL/min/1.73m².
  • 33. Urine Albumin-to-Creatinine Ratio (UACR) — Average of 3 years
    Urine albumin-to-creatinine ratio (UACR) reported as mean ± standard deviation (SD) and median with interquartile range (IQR) in mg/g.
  • 34. Serum Electrolyte Values — Avergae of 3 years
    Serum electrolyte values (sodium, potassium, chloride, bicarbonate) reported individually as mean ± standard deviation (SD) and median with interquartile range (IQR) in mmol/L.
  • 35. Frequency of HbA1c Testing — Average of 3 years
    Frequency of glycated hemoglobin (HbA1c) testing reported as counts and percentages of participants tested per monitoring period.
  • 36. Frequency of Fasting Glucose Testing — Average of 3 years
    Frequency of fasting glucose testing reported as counts and percentages of participants tested per monitoring period.
  • 37. Frequency of Lipid Profile Testing — Average of 3 years
    Frequency of lipid profile testing (total cholesterol, LDL-C, HDL-C, triglycerides) reported as counts and percentages of participants tested per monitoring period.
  • 38. Frequency of Serum Creatinine Testing — Average of 3 years
    Frequency of serum creatinine testing reported as counts and percentages of participants tested per monitoring period.
  • 39. Frequency of eGFR Assessment — Average of 3 years
    Frequency of estimated glomerular filtration rate (eGFR) assessment reported as counts and percentages of participants assessed per monitoring period.
  • 40. Frequency of Urine Albumin-to-Creatinine Ratio Testing — Average of 3 years
    Frequency of urine albumin-to-creatinine ratio (UACR) testing reported as counts and percentages of participants tested per monitoring period.
  • 41. Echocardiography — Average of 3 years
    Frequency of echocardiography abnormalities reported as counts and percentages
  • 42. Electrocardiogram (ECG) — Average of 3 years
    Frequency of electrocardiogram (ECG) abnormalities reported as counts and percentages
  • 43. Participants Receiving Dietary Modification Counseling — Average of 3 years
    Percentage of participants receiving dietary modification counseling or intervention reported as counts and percentages.
  • 44. Participants Enrolled in Exercise Programs — Average of 3 years
    Percentage of participants enrolled in or recommended exercise programs reported as counts and percentages.
  • 45. Participants Receiving Weight Management Interventions — Average of 3 years
    Percentage of participants receiving weight management interventions or counseling reported as counts and percentages.
  • 46. Participants Receiving Smoking Cessation Counseling — Average of 3 years
    Percentage of participants receiving smoking cessation counseling or interventions reported as counts and percentages.
  • 47. Participants Receiving Alcohol Reduction Counseling — Average of 3 years
    Percentage of participants receiving alcohol reduction counseling or interventions reported as counts and percentages.
  • 48. Percentage of Participants by Line of Treatment — Average of 3 years
    Distribution of participants by line of pharmacological treatment (first-line, second-line, third-line or higher) reported as counts and percentages.
  • 49. Percentage of Participants by Drug Class — Average of 3 years
    Distribution of participants by drug class prescribed (e.g., SGLT2i, GLP-1RA, ACEi, ARBs, beta-blockers, MRAs, CCBs, diuretics, metformin, DPP-4i, sulfonylureas, insulin) reported as counts and percentages.
  • 50. Percentage of Participants Undergoing Cardiac Surgeries (CABG or PCI) — Average of 3 years
    Percentage of participants undergoing coronary artery bypass graft (CABG) or percutaneous coronary intervention (PCI) reported as counts and percentages for each procedure type.
  • 51. Percentage of Participants Receiving Dialysis — Average of 3 years
    Percentage of participants receiving dialysis procedures (hemodialysis or peritoneal dialysis) reported as counts and percentages.
  • 52. Percentage of Participants with Cardiac Device Implantation — Average of 3 years
    Percentage of participants with cardiac device implantation (pacemaker, implantable cardioverter-defibrillator \[ICD\], or cardiac resynchronization therapy \[CRT\]) reported as counts and percentages for each device type.
  • 53. Mean Duration of Pharmacological Treatments — Average of 3 years
    Duration of pharmacological treatments reported as mean ± standard deviation (SD) and median with interquartile range (IQR) in months for each drug class.
  • 54. Drug Dose of Pharmacological Treatments — Average of 3 years
    Drug dose of pharmacological treatments prescribed reported as mean ± standard deviation (SD) and median with interquartile range (IQR) in milligrams (mg) for each drug class.
  • 55. Number of Primary Care Visits per Participant — Average of 3 years
    Total number of primary care visits reported as total visits and mean visits per participant ± standard deviation (SD).
  • 56. Number of Tertiary Care Hospital Visits per Participant — Average of 3 years
    Total number of tertiary care hospital visits reported as total visits and mean visits per participant ± standard deviation (SD).
  • 57. Number of Specialist Care Visits per Participant — Average of 3 years
    Total number of specialist care visits reported as total visits and mean visits per participant ± standard deviation (SD).
  • 58.Number of Emergency Department Visits per Participant — Average of 3 years
    Total number of emergency department visits reported as total visits and mean visits per participant ± standard deviation (SD).
  • 59. All-Cause Hospitalizations — Average of 3 years
    All-cause hospitalizations reported as counts, percentages of participants with at least one hospitalization, total hospitalizations, and rate per 100 person-years.
  • 60. Disease-Specific Hospitalizations — Average of 3 years
    Disease-specific hospitalizations (related to T2DM, HTN, HF, or CKD) reported as counts, percentages of participants with at least one hospitalization, total hospitalizations, and rate per 100 person-years.
  • 61. All-Cause Emergency Department Visits — Average of 3 years
    All-cause emergency department visits reported as counts, percentages of participants with at least one visit, total visits, and rate per 100 person-years.
  • 62. Disease-Specific Emergency Department Visits — Average of 3 years
    Disease-specific emergency department visits (related to T2DM, HTN, HF, or CKD) reported as counts, percentages of participants with at least one visit, total visits, and rate per 100 person-years.
  • 63. Length of Hospital Stay — Average of 3 years
    Length of hospital stay reported as median with interquartile range (IQR) and mean ± standard deviation (SD) in days.

Trial sites (76)

FacilityCityRegionStatus
Research Site Fortaleza Ceará Recruiting
Research Site Colatina Espírito Santo (ES) Recruiting
Research Site Salvador Estado de Bahia Recruiting
Research Site Brasília Federal District Recruiting
Research Site Poços de Caldas Minas Gerais Recruiting
Research Site Campina Grande do Sul Paraná Recruiting
Research Site Curitiba Paraná Recruiting
Research Site Teresina Piauí (PI) Recruiting
Research Site Santa Cruz do Sul Rio Grande Do Sul (RS) Recruiting
Research Site Goiânia State of Goias Recruiting
Research Site Joinville State of Santa Catarina Recruiting
Research Site Bragança Paulista São Paulo Recruiting
Research Site São Caetano do Sul São Paulo Recruiting
Research Site São Paulo Brazil Recruiting
Research Site São Paulo Brazil Recruiting
Research Site Providencia Santiago Metropolitan Recruiting
Research Site San José Costa Rica Recruiting
Research Site Abidjan Côte d’Ivoire Recruiting
Research Site Alexandria Egypt Recruiting
Research Site Cairo Egypt Recruiting
Research Site Giza Egypt Recruiting
Research Site Tbilisi Georgia Recruiting
Research Site Kumasi Ghana Recruiting
Research Site Wan Chai Hong Kong Recruiting
Research Site Ahmedabad India Recruiting
Research Site Kolkata India Recruiting
Research Site Mumbai India Recruiting
Research Site Sulaymaniyah Iraq Recruiting
Research Site Aktobe Kazakhstan Recruiting
Research Site Almaty Kazakhstan Recruiting
Research Site Almaty Kazakhstan Recruiting
Research Site Almaty Kazakhstan Recruiting
Research Site Almaty Kazakhstan Recruiting
Research Site Nairobi Kenya Recruiting
Research Site Kuala Lumpur Malaysia Recruiting
Research Site León Guanajuato Recruiting
Research Site Iztapalapa Mexico Recruiting
Research Site Mexico City Mexico Recruiting
Research Site Mexico City Mexico Recruiting
Research Site México Mexico Recruiting

+ 36 more sites — see the full list on the official registry below.

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03549754 on ClinicalTrials.gov ↗ ← All trials in India