Mechanism of Weight Loss After Endoscopic and Laparoscopic Sleeve Procedures

Sponsor
Northwell Health (Other)
Overall Status
Terminated
CT.gov ID
NCT04006002
Collaborator
(none)
4
1
30.9
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Study Details

Study Description

Brief Summary

The purpose of this research study is to understand the mechanism of weight loss for weight loss procedures: that is Laparoscopic sleeve gastrectomy and Endoscopic sleeve Gastroplasty.

Condition or Disease Intervention/Treatment Phase
  • Other: Metabolic and Hormonal profile

Detailed Description

We want to better understand the mechanisms for weight loss by understanding the anatomic and physiologic changes that occur with gastric restrictive procedures for weight loss and to determine the differences in metabolic profile between the two restrictive procedures. We also want to identify the rate of Gastro Esophageal Reflux Disease (GERD) in patients undergoing gastric restrictive procedures for weight loss.

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
4 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
A Pilot Study to Compare Anatomic, Physiologic, Metabolic and Weight Changes After Standard of Care Endoscopic Gastric Restrictive Bariatric Interventions vs. Standard of Care Laparoscopic Sleeve Gastrectomy
Actual Study Start Date :
Jul 1, 2019
Actual Primary Completion Date :
Jun 30, 2021
Actual Study Completion Date :
Jan 28, 2022

Arms and Interventions

Arm Intervention/Treatment
Endoscopic Sleeve Gastrectomy

This group includes all patient who undergo Endoscopic Sleeve Gastrectomy for weight loss

Other: Metabolic and Hormonal profile
To assess changes in metabolic profiles and body metrics such as weight and BMI in these patients after an endoscopic or surgical bariatric intervention

Laproscopic Sleeve Gastrectomy

This group includes all patient who undergo Laproscopic Sleeve Gastrectomy for weight loss

Other: Metabolic and Hormonal profile
To assess changes in metabolic profiles and body metrics such as weight and BMI in these patients after an endoscopic or surgical bariatric intervention

Outcome Measures

Primary Outcome Measures

  1. Percentage of participants with GERD before and after intervention [1 years]

    Percentage of participants with GERD (>6% abnormal esophageal acid exposure calculated via BRAVO pH monitoring for 96 hrs ) before and at 12 months after an endoscopic or surgical bariatric intervention

Secondary Outcome Measures

  1. Compare gastric emptying after intervention [1 year]

    To compare gastric emptying and small bowel transit times, before and at 12 months after an endoscopic or surgical bariatric intervention using wireless capsule technology

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. BMI ≥ 30 Kg/m2 scheduled to undergo a bariatric intervention

  2. Patients who will be undergoing ESG or LSG as part of their clinical care Age between 18 and 75 years.

  3. Both male and female subjects will be included in the study.

  4. Subjects from any ethnic background will be included in the study.

  5. Female participants of childbearing age should not be pregnant. (Pregnancy test will be performed on all women of child bearing potential before any standard of care endoscopic procedure. For the purpose of the study we will record that information in the patient study records).

  6. Successfully complete the screening process.

  7. Patients able to provide written informed consent on the IRB/EC-approved informed consent form.

  8. Demonstrate willingness to follow protocol requirements, including follow-up schedule, and completion of questionnaires.

  9. Having standard of care therapy (endoscopic or laproscopic) for treatment of Obesity.

Exclusion Criteria:
  1. Pregnant or planning to become pregnant during period of study participation.

  2. Female participants who are breast-feeding.

  3. Severe Immunodeficiency.

  4. Severe malnutrition.

  5. The participant has life expectancy of less than 1 year due to other medical conditions.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Northwell Health New York New York United States 10014

Sponsors and Collaborators

  • Northwell Health

Investigators

  • Principal Investigator: Petros Benias, MD, Northwell Health

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Northwell Health
ClinicalTrials.gov Identifier:
NCT04006002
Other Study ID Numbers:
  • 19-0112
First Posted:
Jul 2, 2019
Last Update Posted:
Feb 14, 2022
Last Verified:
Jan 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 14, 2022