Obesity, Morbid
Conditions
Keywords
bariatric surgery, gastric bypass, intestinal obstruction, postoperative complication, methods, laparoscopy
Brief summary
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.
Detailed description
Randomised controlled trials (RCT) are golden standard for assessing interventions in medical science. Due to ethical or practical reasons, RCTs may however not always be feasible. The study objective was to test if the results from the RCT differ from observational data in a setting with a complex surgical intervention. Using the Scandinavian Obesity Surgery Registry database we intend to compare patients operated with laparoscopic gastric bypass surgery within a register based RCT from May 1st 2010 until Nov 14th 2011, with all patients operated with the same procedure registered in the database during the same period of time. Primary end-point measures are severe complications within 30 days (safety outcome) and surgery for small bowel obstruction (efficacy outcome) within 4 years.
Interventions
PROCEDUREclosure of mesenteric defects
Closure of mesenteric defects by use of non-absorbable running sutures in RCT; and according to the choice of the surgeon in the non-RCT
PROCEDUREnon-closure of mesenteric defects
Mesenteric defects are left open
Sponsors
The Scandinavian Obesity Surgery Registry
Region Örebro County
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| severe postoperative complications within 30 days | 30 days | Specified as Clavien-Dindo grade 3b or more |
| reoperation for small bowel obstruction | 4 years | 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 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| postoperative length of stay | 30 days | — |
| length of the operation | intraoperative | — |
| specific postoperative complications | 30 days | 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 |
| weight-loss at 2 years after surgery | 2 years | specified as excessive weight-loss (% excess weight loss = 100 x \[initial weight-postoperative weight\]/\[initial weight-weight corresponding to BMI 25 kg/m2\]) |
Outcome results
None listed