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Program on Surgical Control of Hyperlipidemias (POSCH)

This study has been completed.
Study NCT00000490.   Last updated on June 23, 2005.   Information provided by National Heart, Lung, and Blood Institute (NHLBI)

This Tabular View shows the required WHO registration data elements as marked by

Descriptive Information Fields
Brief Title  Program on Surgical Control of Hyperlipidemias (POSCH)
Official Title 
Brief Summary

To determine whether a profound reduction in serum cholesterol level, induced and maintained by partial ileal bypass, would prevent a second heart attack among men and women who had one myocardial infarction and whose blood cholesterol could not be reduced sufficiently by diet.

Detailed Description

BACKGROUND:

The correlative evidence linking elevated cholesterol to increased risk of cardiovascular disease is incontrovertible. Animal studies have shown that significant reductions in disease in humans may be forthcoming if blood lipids are reduced from elevated levels. Beginning in the 1960s, some patients had undergone a surgical bypass procedure for hyperlipidemia. Patients were selected for surgery after dietary management had been carried out for three years. The average serum cholesterol concentrations decreased markedly and the decrease was sustained.

This grant-supported clinical trial attempted to determine the effect on cardiovascular morbidity and mortality of the partial ileal bypass in patients who had suffered a myocardial infarction within the previous 5 years and who had serum cholesterol over 220 mg deciliter (200 mg if LDL cholesterol was over l40 mg).

DESIGN NARRATIVE:

Randomized, non-blind, fixed sample study with a control group and an experimental group of equal size. The experimental group received a partial ileal bypass and diet therapy to reduce serum cholesterol and triglycerides. The control group was given conventional medical therapy exclusive of cholesterol-lowering drugs. The primary endpoint was death due to any cause. Secondary endpoints included death due to atherosclerosis and morbidity from recurrent myocardial infarction, unstable angina, cerebrovascular accident. Other secondary endpoints included coronary artery bypass surgery, percutaneous transluminal coronary angioplasty, cardiac transplantation, and peripheral vascular surgery.

Beginning in January 1993, long-term morbidity and mortality follow-up are continuing through December 1997 under grant support (R01HL49522). Follow-up includes tracking morbidity and mortality by an annual telephone survey and review of patient records, including death and autopsy results. In addition, mortality and morbidity will be correlated with lipid changes and existing arteriographic results. The long-term course of control patients treated with the AHA Phase II Diet counseling will be assessed and the long-term side effects of partial ileal bypass will be evaluated.

Study Phase Phase III
Study Type  Interventional
Study Design  Prevention, Randomized
Primary Outcome Measure 
Secondary Outcome Measure 
Condition  Cardiovascular Diseases
Coronary Disease
Heart Diseases
Myocardial Infarction
Myocardial Ischemia
Intervention  Procedure: jejunoileal bypass
Behavioral: diet, fat-restricted
MEDLINE PMIDs 8862377,   8857853,   834123,   748369,   222301,   7398005,   7264481,   6750834,   6759035,   6838688,   6613866,   4082609,   4025120,   3899372,   3751907,   3528373,   3307368,   3440393,   2890362,   3303402,   2461778,   3341527,   3073042,   2685177,   2406359,   2205799,   2244557,   2120785,   1877445,   1895677,   1645643,   1309084,   1575819,   1301017,   1417188,   1512911,   8119065,   8482933,   8447332,   7900613,   7695177,   7897460,   7608434,   9625405,   9488536,   9690924,   11137103
Links
Recruitment Information Fields
Recruitment Status  Completed
Enrollment 
Start Date  June 1973
Completion Date December 1997
Eligibility Criteria 

Men and women, ages 30 to 64. Had one myocardial infarction. Had hyperlipoproteinemia.

Gender Both
Ages 30 Years to 64 Years
Accepts Healthy Volunteers No
Contacts ††
Location Countries 
Administrative Information Fields
NCT ID  NCT00000490
Organization ID 9
Secondary IDs ††
Study Sponsor  National Heart, Lung, and Blood Institute (NHLBI)
Collaborators ††
Investigators 
Investigator:     Henry Buchwald     University of Minnesota    
Information Provided By National Heart, Lung, and Blood Institute (NHLBI)
Verification Date June 2001
First Received Date  October 27, 1999
Last Updated Date June 23, 2005

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.




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