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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04325581
Other study ID # pgi123
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date August 1, 2016
Est. completion date December 31, 2018

Study information

Verified date March 2020
Source Postgraduate Institute of Medical Education and Research
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Investigators postulate that the metabolic effects of LSG would be augmented with the use of liraglutide leading to additional excess weight loss, improved glucose homeostasis, decreased intrapancreatic and intrahepatic fat than either of them individually. However there are no studies till date which have evaluated the combined effects of two modalities of weight loss on the above mentioned parameters. This study plans to compare the effects of liraglutide in post- LSG obese patients in a placebo controlled design.


Description:

Various studies have shown that bariatric surgery is associated with significant durable weight loss with associated improvement in obesity related comorbidities and quality of life. The degree of effect on obesity related comorbidities depends on the bariatric surgery approach, typically classified as restrictive and/or malabsorptive effect. Data from International Federation for the Surgery of Obesity and Metabolic Diseases states that most common surgical procedures being performed are Roux-en-Y gastric bypass (45%), sleeve gastrectomy(37%), adjustable gastric banding(10%) and biliopancreatic division with or without duodenal switch(2.5%)5. . LSG is technically a simpler procedure compared to RYGB with lesser operative and long term nutritional complications. The mechanism for weight loss in laparoscopic sleeve gastrectomy is gastric restriction and possible changes in gut hormones resulting from higher level of GLP-1, and lower levels of ghrelin, as a consequence of resection of gastric fundus.

Therefore,investigators postulate that the metabolic effects of LSG would be augmented with the use of liraglutide leading to additional excess weight loss, improved glucose homeostasis, decreased intrapancreatic and intrahepatic fat than either of them individually. However there are no studies till date which have evaluated the combined effects of two modalities of weight loss on the above mentioned parameters. This study plans to compare the effects of liraglutide in post- LSG obese participants in a placebo controlled design.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date December 31, 2018
Est. primary completion date December 31, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Subjects diagnosed with obesity who have elected to undergo bariatric surgery

- Body mass index greater than 27.5kg/mt2

- Ability and willingness to co-operate with follow up.

Exclusion Criteria:

Decompensated liver disease ( child-turcotte pugh score >7)

- Impaired renal function, defined as eGFR< 45 ml/min/m2

- Clinically significant active cardiovascular disease including history of myocardial infarction within the past 6 months and/or heart failure (New York Heart Association (NYHA) class III and IV)

- Recurrent major hypoglycemic episodes

- Use of drugs like systemic corticosteroids, thiazolidinediones, DPPIV inhibitors

- Pregnancy or lactation

- History of pancreatitis or pancreatic cancer

- History of medullary thyroid cancer

- Family history of medullary thyroid cancer

- Contraindications to liraglutide or any of its excipients

- Hypersensitivity to liraglutide or similar drugs

- Patients currently using GLP-1 analogs

- Suspected or known abuse of alcohol

- Presence of secondary cause of obesity.

- Presence of an eating disorder or other psychiatric disorder.

- Prior gastric surgery.

- Unfit for surgery due to severe cardiac, pulmonary diseases or due to any reason.

- Contraindications to MRI scanning

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Liraglutide 6 MG/ML
Liraglutide in incremental dose upto maximum of 1.8 mg per day SC daily
Placebos
Normal Saline SC daily

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Postgraduate Institute of Medical Education and Research

Outcome

Type Measure Description Time frame Safety issue
Primary Incretin change Changes in GLP-1 levels during 2hour OGTT baseline and at 6weeks and 6months after laparoscopic sleeve gastrectomy
Primary Changes in indices of insulin resistance HOMA-IR calculated from fasting insulin and fasting glucose baseline and at 6weeks and 6months after laparoscopic sleeve gastrectomy
Primary Change in pancreatic steatosis Change in pancreatic steatosis would be determined using NUTS ACORN NMR software baseline and 6months after laparoscopic sleeve gastrectomy
Secondary body weight The change in body weight baseline and 6 weeks, 12weeks, 18weeks and 24weeks after surgery
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