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Clinical Trials in Norway / NCT00626964
Active, not recruiting Observational

Prevention of Coronary Heart Disease in Morbidly Obese Patients

NCT00626964 · tracked via the Priya Life Science Norway tracker
Phase
Observational
Started
2008-02
Last updated
2025-06-11

Condition(s) studied

Morbid ObesityHypertensionType 2 DMObstructive Sleep ApneaOsteoarthrosis

Investigational drug(s) / intervention(s)

Bariatric SurgeryConservative Treatment:

Bariatric Surgery: Bariatric Surgery Treatment: Duodenal Switch, Gastric Sleeve or Gastric bypass.

Conservative Treatment:: Intensive Lifestyle Intervention Program

Study summary

The changes in risks of developing coronary heart disease in patients with morbid obesity after different weight loss interventions have not been extensively studied. The primary objective of this study is to investigate whether an intensive lifestyle intervention program in a tertiary care clinic (Spesialsykehuset for Rehabilitering) is comparable with a 7-week low-energy-diet followed by bariatric surgery in decreasing the risk of cardiovascular disease in these patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: * Morbidly Obese patients with BMI \> 40, or BMI \> 35 with comorbidity such as Hypertension, Obstructive Sleep Apnea, Weight Related Osteoarthrosis, Type 2 DM. Exclusion Criteria: * Participation in other weight loss program the last 12 months. Serious psychiatric conditions

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Morbid Obesity Center, Vestfold Hospital Trust Tønsberg Norway

More The Hospital of Vestfold trials in Norway

Other trials for the same condition

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 NCT00626964 on ClinicalTrials.gov ↗ ← All trials in Norway