search
Back to results

Antireflux Efficacy of Hiatal Hernia Repairs in Sleeve Gastrectomy Patients

Primary Purpose

Gastroesophageal Reflux

Status
Terminated
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Sleeve gastrectomy
Hiatal Hernia repair
Sponsored by
Hopital du Sacre-Coeur de Montreal
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Gastroesophageal Reflux focused on measuring Sleeve Gastrectomy, Gastroesophageal reflux, Bariatric Surgery, Complications

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All obese patients with a BMI between 35-50
  • Aged 18-65 and undergoing surgery for a Sleeve Gastrectomy in institution's bariatric surgery department

Exclusion Criteria:

  • hiatal hernias greater than 2 cm,
  • hiatal repair requiring mesh placement
  • prior bariatric surgery or any other counterindication to Sleeve Gastrectomy

Sites / Locations

  • Hopital Sacré-Coeur de Montréal

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Sleeve Gastrectomy group

Sleeve Gastrectomy + Hiatal Hernia repair group

Arm Description

This group will receive a Sleeve Gastrectomy only, a mainly restrictive procedure which consists in creating a narrow tube-like stomach based on its lesser curvature.

This group will receive a Sleeve Gastrectomy combined with hiatal hernia repair. Hiatal Hernia repair consists of a peri-esophageal dissection proximal to the diaphragmatic crura to achieve an intra-abdominal esophageal length of 2-3 cm. The pillars will then be closed anteriorly and posteriorly using nonabsorbable sutures.

Outcomes

Primary Outcome Measures

Change in the presence of pathological Gastroesophageal reflux disease (GERD)
Pathological GERD will be assessed objectively using a 24 hour pH study and an EGD (esophagogastroduodenoscopy - presence of esophagitis)

Secondary Outcome Measures

Presence of hiatal hernia (intrathoracic migration of the sleeve)
Presence of hiatal hernia will be assessed using EGD and high-resolution esophageal manometry
Presence of hypotensive lower esophageal sphincter (LES)
Hypotensive LES will be measured objectively using a high-resolution esophageal manometry study
Worsening or new-onset gastroesophageal reflux disease
Worsening or new-onset gastroesophageal reflux disease will be measured using a validated reflux questionnaire (GERD-HRQL). The GERD-HRQL questionnaire was developed and validated to measure changes of typical GERD symptoms such as heartburn and regurgitation in response to surgical or medical treatment. Total Score: Calculated by summing the individual scores to questions 1-15. Greatest possible score (worst symptoms) = 75 Lowest possible score (no symptoms) = 0

Full Information

First Posted
June 7, 2019
Last Updated
November 30, 2022
Sponsor
Hopital du Sacre-Coeur de Montreal
search

1. Study Identification

Unique Protocol Identification Number
NCT04433507
Brief Title
Antireflux Efficacy of Hiatal Hernia Repairs in Sleeve Gastrectomy Patients
Official Title
Antireflux Efficacy of Hiatal Hernia Repairs Concomitant to Sleeve Gastrectomy in Obese Patients (BMI 35-50)
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Terminated
Why Stopped
Recruitment issues
Study Start Date
April 1, 2019 (Actual)
Primary Completion Date
September 1, 2021 (Actual)
Study Completion Date
September 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hopital du Sacre-Coeur de Montreal

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Gastroesophageal reflux (GR) occurrence or persistence following a sleeve gastrectomy (SG) can be correlated to several factors but it is clear that one of the key factors is a persistent hiatal hernia or laxity of the esophageal hiatus. However, there are no clear guidelines presently available on surgical management of small size hernias or an abnormal hiatus. Therefore, hiatal hernia management is decided intraoperatively by the operating surgeon. The main goal of this study is to evaluate the efficacy of primary hiatal hernia repairs on gastroesophageal reflux concomitant to sleeve gastrectomy. The secondary objectives are hiatal hernia recurrence following primary surgery and the occurrence of "de novo" GR.
Detailed Description
Background : The Sleeve gastrectomy (SG) is the most common bariatric procedure worldwide because it is the simplest to perform, from a technical standpoint, and the most efficient in terms of metabolic control and weight loss. However, this intervention can lead to several complications, including the onset or intensification of gastroesophageal reflux (GR) with the associated impact on the patients' quality of life and a possible evolution into Barrett's esophagus. One of the key factors in the development of this complication is a persistent hiatal hernia. Aims: The main objective of this study is to provide an objective evaluation of the effect of primary hiatal hernia repair on GR concomitant to sleeve gastrectomy. The secondary objectives are hiatal hernia recurrence following primary surgery and the occurrence of "de novo" GR. Methods : A total of 100 patients will be recruited for the pilot study, with 50 patients in the SG group and 50 in the SG + primary hiatal hernia repair group following randomization. Then, based on a sample size study, recruitment will be continued as needed. None of the procedures performed are experimental. All obese patients with a BMI between 35-50, aged 18-65 and undergoing surgery for a SG in the institution's bariatric surgery department will be eligible to participate in this study. Exclusion criteria will be hiatal hernias greater than 2 cm, a hiatal repair requiring a drain, prior bariatric surgery or any other counterindication to SG. All patients will be evaluated preoperatively using: 1) EGD, 2) esophageal manometric study, 3) pH assessment and 4) validated GR questionnaires (GERD-HRPL; GCSI). Iconographic intraoperative data on hiatal morphology and the type of cure used will be collected and records will be kept according to Ethics committee guidelines. After a 6-month follow-up the participants will undergo the same tests, including questionnaires, for a medium-term profile.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastroesophageal Reflux
Keywords
Sleeve Gastrectomy, Gastroesophageal reflux, Bariatric Surgery, Complications

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
50 patients in the SG group and 50 in the SG + primary hiatal hernia repair group following randomization
Masking
None (Open Label)
Allocation
Randomized
Enrollment
16 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sleeve Gastrectomy group
Arm Type
Active Comparator
Arm Description
This group will receive a Sleeve Gastrectomy only, a mainly restrictive procedure which consists in creating a narrow tube-like stomach based on its lesser curvature.
Arm Title
Sleeve Gastrectomy + Hiatal Hernia repair group
Arm Type
Experimental
Arm Description
This group will receive a Sleeve Gastrectomy combined with hiatal hernia repair. Hiatal Hernia repair consists of a peri-esophageal dissection proximal to the diaphragmatic crura to achieve an intra-abdominal esophageal length of 2-3 cm. The pillars will then be closed anteriorly and posteriorly using nonabsorbable sutures.
Intervention Type
Procedure
Intervention Name(s)
Sleeve gastrectomy
Intervention Description
Laparoscopic sleeve gastrectomy (LSG) is performed through a standard 5-port technique. After dissection of the greater curvature of the stomach, a narrow tube-like stomach is created after stapling off the lateral aspect of the stomach using a 40 French bougie as a guide.
Intervention Type
Procedure
Intervention Name(s)
Hiatal Hernia repair
Intervention Description
Hiatal hernia repair consists in a circumferential dissection of the diaphragmatic crura to achieve an intra abdominal esophageal length of 2-3 cm. The crura will then be closed anteriorly and posteriorly using nonabsorbable sutures.
Primary Outcome Measure Information:
Title
Change in the presence of pathological Gastroesophageal reflux disease (GERD)
Description
Pathological GERD will be assessed objectively using a 24 hour pH study and an EGD (esophagogastroduodenoscopy - presence of esophagitis)
Time Frame
Before surgery and 6 months after surgery
Secondary Outcome Measure Information:
Title
Presence of hiatal hernia (intrathoracic migration of the sleeve)
Description
Presence of hiatal hernia will be assessed using EGD and high-resolution esophageal manometry
Time Frame
Before surgery and 6 months postoperative
Title
Presence of hypotensive lower esophageal sphincter (LES)
Description
Hypotensive LES will be measured objectively using a high-resolution esophageal manometry study
Time Frame
before the surgery and 6 months post-operative
Title
Worsening or new-onset gastroesophageal reflux disease
Description
Worsening or new-onset gastroesophageal reflux disease will be measured using a validated reflux questionnaire (GERD-HRQL). The GERD-HRQL questionnaire was developed and validated to measure changes of typical GERD symptoms such as heartburn and regurgitation in response to surgical or medical treatment. Total Score: Calculated by summing the individual scores to questions 1-15. Greatest possible score (worst symptoms) = 75 Lowest possible score (no symptoms) = 0
Time Frame
before the surgery and 6 months post-operative

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All obese patients with a BMI between 35-50 Aged 18-65 and undergoing surgery for a Sleeve Gastrectomy in institution's bariatric surgery department Exclusion Criteria: hiatal hernias greater than 2 cm, hiatal repair requiring mesh placement prior bariatric surgery or any other counterindication to Sleeve Gastrectomy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Radu Pescarus, MD
Organizational Affiliation
Hopital Sacré Coeur de Montréal
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hopital Sacré-Coeur de Montréal
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H4J 1C5
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Antireflux Efficacy of Hiatal Hernia Repairs in Sleeve Gastrectomy Patients

We'll reach out to this number within 24 hrs