Obesity, Morbid Clinical Trial
Official title:
Comparing a Randomised Controlled Intervention With Observational Data.
Verified date | October 2016 |
Source | Region Örebro County |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Comparison of participants in a randomised controlled trial (RCT) with observational data from patients operated in Sweden during the same period of time. The primary objective is to compare effects from a complex surgical intervention from RCT and observational data.
Status | Completed |
Enrollment | 10992 |
Est. completion date | May 2016 |
Est. primary completion date | December 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - The same as acceptance criteria for bariatric surgery according to the 1991 NIH Consensus Statement Exclusion Criteria: - retrocolic gastric bypass procedure - previous bariatric procedures - primary open procedures - missing data on handling of the mesenteric defects |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Region Örebro County | The Scandinavian Obesity Surgery Registry |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | severe postoperative complications within 30 days | Specified as Clavien-Dindo grade 3b or more | 30 days | |
Primary | reoperation for small bowel obstruction | Efficacy outcome: Number of participants with reoperation due to small bowel obstruction defined as acute symptoms of bowel obstruction with findings suggestive of small bowel obstruction during surgery | 4 years | |
Secondary | postoperative length of stay | 30 days | ||
Secondary | length of the operation | intraoperative | ||
Secondary | specific postoperative complications | leakage or deep intra-abdominal infection, bleeding requiring intervention, small bowel obstruction/ileus, port-related complications, wound dehiscence, other wound complications (mainly superficial wound infections), anastomotic stricture, marginal ulcer, cardiovascular length of the operation event, pulmonary complication (other than pulmonary embolism), venous thromboembolism (including pulmonary embolism), urinary tract infection and other (in this case specified) complication | 30 days | |
Secondary | weight-loss at 2 years after surgery | specified as excessive weight-loss (% excess weight loss = 100 x [initial weight-postoperative weight]/[initial weight-weight corresponding to BMI 25 kg/m2]) | 2 years |
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