Laparoscopic Sleeve Gastrectomy With or Without Hiatal Hernia Repair in Morbidly Obese Patients

Not Applicable

Recruiting

• Conditions: Morbid Obesity; Hiatal Hernia; Gastroesophageal Reflux Disease; Sleeve Gastrectomy

• Registration Number: NCT03776669
• Lead Sponsor: National Taiwan University Hospital

Brief Summary

Background:

Obesity and hiatal hernia are both risk factors of gastroesophageal reflux disease (GERD), and the incidence of hiatal hernia is much higher in morbidly obese patients. Many believe that higher intra-abdominal pressure with higher esophagogastric junction (EGJ) pressure gradient in morbidly obese patients is the main mechanism accounting for the occurrence of GERD. Hiatal hernia, on the other hand, is associated with structure abnormality of EGJ. Sleeve gastrectomy (SG) has been becoming a standalone bariatric surgery for decades, and it has been proved to effectively induce long-term weight loss in morbidly obese patients. Some studies found morbidly obese patients benefited from resolution of GERD after SG, however, other studies had the opposite findings. Some morbidly obese patients had aggravating GERD or de novo GERD after SG. The mechanism is still unclear now. It might result from removal of fundus and sling muscular fibers of EGJ, increased intra-gastric pressure (IIGP), and hiatal hernia after surgery. High resolution impedance manometry (HRIM) is used to access esophageal and EGJ function objectively. Impedance reflux was more frequently observed in patients having gastroesophageal reflux (GER) symptoms after SG. In addition, previous studies also found decreased EGJ resting pressure, decreased length of lower esophageal sphincter (LES), and presence of hiatal hernia were associated with more GERD after SG.

Objective:

To evaluate the long-term EGJ function and GERD in morbidly obese patients with hiatal hernia receiving laparoscopic sleeve gastrectomy (LSG) with or without hiatal hernia repair (HHR).

Detailed Description

Patients and methods:

A total of 70 patients will be recruited and randomized to two groups with a 1:1 allocation ratio. Patients in the control group receive LSG alone and in the experimental group receive LSG with HHR. All subjects should provide basic clinical and demographic information, be evaluated for GER symptoms using GerdQ score, sign informed consent, and complete preoperative abdominal computed tomography (CT) scan, esophagogastroduodenoscopy (EGD), and HRIM. Outpatient follow-up would be arranged 1 weeks after discharge, then 1 month, 3 months, 6 months, and 12 months after surgery. Weight change and GER symptoms will be evaluated at every outpatient visit. Abdominal CT scan, EGD, and HRIM will be performed 12 months after surgery.

Expected results:

Less reflux esophagitis, less impedance reflux episodes, lower incidence of hiatal hernia, higher EGJ resting pressure, and longer LES length should be observed in morbidly obese patients receiving LSG with HHR at 12-month follow-up, using EGD and HRIM as evaluation tools. Furthermore, lower GerdQ score should be observed in these patients.

Study Timeline

• Study First Submitted: 2018-12-13
• Study First Submitted QC: 2018-12-13
• Study First Posted: 2018-12-17
• Study Start: 2019-01-09
• Status Verified: 2022-01
• Last Update Submitted: 2022-01-19
• Last Update Posted: 2022-01-21
• Primary Completion: 2023-11-01
• Study Completion: 2024-12-17

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

• Patients with:

  1. Body mass index (BMI) ≧ 35, or
  2. 30 ≦ BMI < 35, with inadequately controlled type 2 diabetes mellitus (T2DM) or metabolic syndrome, or
  3. T2DM with BMI ≧ 32.5, or
  4. T2DM with BMI between 27.5 and 32.5 not well controlled by medication, especially for those with major cardiovascular risk.

• Age: 20 to 65 years old.

• Hiatal hernia diagnosed by either:

  1. HRIM: defined as the distance between low esophageal sphincter (LES) and crural diaphragm (CD) equal to or greater than 2 cm. (LES-CD ≧ 2 cm)
  2. EGD: defined as the apparent separation between the squamocolumnar junction and the diaphragmatic impression is greater than 2 cm.

Exclusion Criteria

• Prior major gastrointestinal (GI) tract surgery.

• Bleeding tendency.

• American Society of Anesthesiologists physical status (ASA) ≧ class III.

• Pregnancy or lactating women.

• Allergy to contrast medium for CT scan.

• Concomitantly untreated or uncontrolled endocrine disease.

• Alcohol or drug abuse.

• Mental, behavioral, and neurodevelopmental disorders.

  1. Patients who possess "National Health Insurance (NHI) Major Illness/Injury Certificate" for ICD-10-CM codes F01-F99. (ICD: International Classification of Diseases; CM: Clinical Modification)
  2. Patients who have been hospitalized in psychiatric ward in the recent one year.

• Type IV hiatal hernia.

• Moderate to severe reflux esophagitis (LA classification grade B/C/D) refractory to medical treatment.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
De novo reflux esophagitis	Within 12 months after surgery if symptomatic or at 12 months if asymptomatic.	Los angles classification grade B/C/D reflux esophagitis diagnosed by esophagogastroduodenoscopy.

Secondary Outcome Measures

Name	Time	Method
Impedance reflux	12 months after the surgery	Impedance reflux after single swallow by high resolution impedance manometry
GerdQ score	At 1 week (± 1 week) after discharge, then 1 month (± 2 weeks), 3 months (± 1 month), 6 months (± 1 month), and 12 months (± 1 month) after surgery.	Questionnaire for gastroesophageal reflux symptoms
Lower esophageal sphincter (LES) length	12 months after the surgery	Measured by high resolution impedance manometry
Post-operative complication	Within 30 days of surgery	Defined as complication ≧ grade III Clavien-Dindo classification
Esophagogastric junction (EGJ) resting pressure	12 months after the surgery	Measured by high resolution impedance manometry
De novo or aggravating hiatal hernia	12 months after the surgery (or within 12 months after surgery if symptomatic )	Diagnosed by high resolution impedance manometry or esophagogastroduodenoscopy.
Mesh-related complication	Within 12 months after surgery	infection, allergic reaction, intestinal complication, fistula formation, seroma formation, hematoma, recurrence of tissue defect, dysphagia, esophageal erosion or perforation.

Trial Locations

Locations (1)

National Taiwan University Hospital; 🇨🇳 Taipei, Taiwan