Clinical Trials in India / NCT03549754
Recruiting
Observational
iCaReMe Global Registry: Multinational Real-world Evidence in Cardiorenal and Metabolic Diseases
NCT03549754 · tracked via the Priya Life Science India tracker
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| 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.
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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