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30-Days Post-Operative Complications in Bariatric Surgery

Comparison of Laparoscopic Sleeve Gastrectomy (LSG) With Laparoscopic Gastric Bypass (LRYGB) in Bariatric Surgery; 30-Days Post-Operative Complications in Bariatric Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04779723
Acronym
Bariatric
Enrollment
116
Registered
2021-03-03
Start date
2018-06-13
Completion date
2019-10-12
Last updated
2021-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bariatric Surgery

Keywords

Bariatric surgery, Laparoscopic Roux-en-Y gastric bypass, Laparoscopic sleeve gastrectomy

Brief summary

comparison of 30-days post-operative outcomes of laparoscopic sleeve gastrectomy (LSG) and laparoscopic Roux-en-Y gastric bypass (LRYGB)

Detailed description

Obesity is one of the most challenging chronic diseases in the western world as well as in Pakistan. Half of the people in this world consider themselves overweight or obese. Obesity is one of the most challenging chronic diseases in the western world as well as in Pakistan . Half of the people in this world consider themselves overweight or obese. Obesity is challenging to control by medical therapy and drug treatment. The most effective way to treat obesity is bariatric surgery. Laparoscopic Roux-en-Y gastric bypass (LRYGB) is a gold standard bariatric surgical procedure. Recently there is much attention gained by laparoscopic sleeve gastrectomy (LSG). Therefore, we decided to conduct this comparative study to compare the early post-op complications of LSG with LRYGB technique in patients undergoing bariatric surgery.

Interventions

PROCEDUREComparison of two Techniques of bariatric surgery

We compared the 30 days outcomes in patients who underwent LSG procedure with those who underwent LRYGB

Sponsors

Multan Medical And Dental College
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* patients of age 18 to 65 years * body mass index (BMI) \>35 kg/m2 (Morbidly obese) * Patients with failed conservative treatment of weight control

Exclusion criteria

* Severe indicative gastroesophageal reflux disease (GERD) * Conversion of another bariatric procedure * Large hiatal hernia * Patients with inflammatory bowel disease

Design outcomes

Primary

MeasureTime frameDescription
Frequency of Anastomotic Leakage in Each Study Armwithin the first 30 days after surgeryPatients were examined on postoperative 30 days for the presence of Anastomotic leakage
Frequency of Bleeding in Each Study Arm24 hours after surgeryPatients were examined postoperative for the presence of bleeding
Number of Infections in Each Study Arm30 daysPatients were examined on postoperative 30 days for the presence of Wound infections
Mortality in Each Study Arm30 daysPatients were followed for 30 days and number of mortalities was noted on each arm

Secondary

MeasureTime frameDescription
Hospital Stay30 daysDuration of hospitalization

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026