Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05365087
Other study ID # LMC2021-1001
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date March 1, 2018
Est. completion date December 31, 2032

Study information

Verified date March 2024
Source Lexington Health Incorporated
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A retrospective and prospective cohort study to compare the effect of completing a Transoral Fundoplication (TF) procedure prior to Laparoscopic Sleeve Gastrectomy (LSG) surgery to Laparoscopic Roux-en-Y Gastric Bypass (LRYGB) in bariatric patients with Gastroesophageal Reflux Disease (GERD) signs and symptoms. The aim of this study is to examine the effect of TF prior to sleeve gastrectomy as compared to Roux-en-Y Gastric Bypass on reflux symptoms in bariatric patients. Additional Follow up data until 10 years will be collected to evaluate for sequelae of GERD.


Description:

Gastroesophageal Reflux Disease (GERD) is a common condition that produces discomfort and can result in serious sequelae from frequent esophageal acid exposure, including Barrett's esophagus, erosive esophagitis, esophageal adenocarcinoma, voice changes, and asthma exacerbation. The prevalence of GERD in adults continues to increase in conjunction with the increase in obesity. Because obesity and GERD are clearly linked, an individual with obesity is four times more likely to develop esophageal carcinoma than in an individual with a normal BMI(Valezi, et al,2018). Additionally, the incidence of GERD is proportional to rising BMI ranging from 23 to 50%. Weight loss is associated with decreased GERD symptoms(Mion, & Dargent,2014). Bariatric surgery has proven to be effective in reducing BMI, which subsequently often reduces GERD. The laparoscopic sleeve gastrectomy (LSG) is an effective weight loss tool; however, recent literature suggests a correlation of de novo or worsening reflux symptoms in bariatric patients within one year postoperatively, independent of weight loss. A study conducted by Tai,et al,.(2013) found that the prevalence of GERD symptoms increased significantly from 12.1% to 47% after LSG. Additionally, of the 58 patients in the study who were asymptomatic prior to surgery, 44.8% developed GERD symptoms after LSG. Other studies have found that among patients with no preoperative GERD, 86% developed symptoms postoperatively.(Dupree, et al.,2014) The Laparoscopic Roux-en-Y gastric bypass (LRYGB) has been touted as the gold standard to treat both obesity and GERD; however, this procedure has a higher morbidity rate. While LSG has relatively low rates of re-operations, the LRYGB carries significant lifetime risk for multiple operative procedures due to adhesive bowel obstruction, internal hernia, non-healing ulcers and intussusception.(Zak, et al.,2016) Furthermore, nutrient malabsorption following LRYGB can result in irreversible neurological complications, and accelerated, ongoing decline in bone mineral density.(Pizzorno,2016). Options for surgical correction of GERD are limited following bariatric surgery. However, options for anti-reflux procedures prior to undergoing bariatric surgery are viable, and may include Transoral Fundoplication (TF). Transoral fundoplication is an anti-reflux procedure which has proven to achieve long-lasting relief of gastroesophageal reflux symptoms, and eliminate, or reduce the use of proton pump inhibitors (PPI). Daily dependence on PPI's were eliminated in 75-80% of cases for up to six years in a 2014 study conducted by Testoni et al.. Although a TF procedure is not an option post bariatric surgery due to technical issues, it is available prior to LSG. With these surgeries working in tandem, patients may attain the benefits of both, as they are reciprocal in nature: TF provides anti-reflux barriers and LSG enables patients to lose weight, which ultimately decreases GER symptoms. We propose that performing a TF procedure prior to a sleeve gastrectomy will result in a decrease in GERD symptoms similar to that of a LRYGB. In addition to evaluating symptoms, we will perform endoscopy screening post bariatric surgery at 1,3,5,and 10 years or more often as indicated , to assess for asymptomatic GERD and its sequelae.. Population to be Reviewed 1. Patient Identification 1. Patients seen for bariatric surgery consultation who report a history or current symptoms of GERD, or who are taking some form of medication for treatment of GERD, are asked to complete the Gastroesophageal Reflux Disease-Health Related Quality of Life Questionnaire (GERD-HRQL). The GERD-HRQL is a validated, reliable and practical standard instrument which assesses the impact and severity of reflux symptoms on a patient's quality of life. The use of the GERD-HQRL for this purpose reflects a standard of care in the evaluation of any patient presenting with GERD symptoms. 2. The GERD-HRQL consists of 11 questions which focus on disease symptoms such as heartburn, difficulty swallowing, bloating, and pain, as well as the effect of these symptoms on daily life and an individual's satisfaction with their current condition. Symptoms are scored from 0 to 5 (0= no symptoms, 1= symptoms noticeable but not bothersome, 2= symptoms noticeable and bothersome but not every day, 3= symptoms bothersome every day, 4= symptoms affect daily activities, 5= symptoms are incapacitating, and unable to do activities). The summation of this score represents the severity and frequency of typical GERD symptoms. A score of 13 or higher on the GERD-HRQL warrants further diagnostic workup which may include the following: esophagogastroduodenoscopy, esophageal ambulatory pH study, esophageal manometry, and an upper gastrointestinal series (UGI). 3. Each patient is then presented at the GERD conference where treatment options are discussed and determined. The GERD conference is a multi-disciplinary meeting in which the patient's diagnostic results are presented in consideration of their personal history and comorbidities; based on these results, medical history and present status, treatment plans are discussed in order to provide the patient with the best possible outcome. 4. Treatment options are then presented to the patient, who ultimately decides the course of action. In general, patients are allowed to choose the surgical option that meets their treatment goals if they are able to demonstrate a clear understanding of the risks, benefits and indications for each choice. Therefore, patients are not randomized to one procedure. 5. GERD conferences will be retrospectively reviewed from March 2018 to February 2020 to identify bariatric patients with GERD who chose to undergo the TF procedure followed by the LGS or LRNGB. Thereafter, a continuing review following each GERD conference identifies patients suitable for study inclusion. 6. Patients who chose to undergo the TF to Sleeve route or who chose to undergo the LRYGB will be asked to consider consenting for their information to be part of this study. All patients who meet the proposal criteria will be approached by the study researchers until there are 60 patients enrolled in each category. Upon agreement, the patient's consent of the study will be appropriately documented. 7. Patients who choose LSG or TF to LSG will undergo screening endoscopies at the following postoperative LSG intervals: 12 months, three years, five years and 10 years. 8. A cohort of 60 patients who presented preoperatively with no evidence of GERD and underwent LSG, and who complete standard surveillance endoscopy postoperatively will be included in the study to provide a baseline from which to compare effectiveness of treatment.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 180
Est. completion date December 31, 2032
Est. primary completion date December 31, 2032
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Bariatric patients who have documented GERD per GERD-HRQL at initial consultation and confirmed by preoperative testing - 60 bariatric patients who received or plan to have the TF procedure prior to Sleeve Gastrectomy - 60 bariatric patients who underwent or plan to undergo Roux-en-Y Gastric Bypass - Male or female - Ages 18 or older - Bariatric patients who have no evidence of GERD per GERD-HRQL at initial consultation or on preoperative testing. - 60 bariatric patients who received or plan to undergo LSG and who complete surveillance endoscopy one year postoperatively Exclusion Criteria: - Incomplete records missing any component of the demographic data to be analyzed - Patients who undergo Roux-en-Y Gastric Bypass conversion from Sleeve Gastrectomy

Study Design


Intervention

Procedure:
Transoral Fundoplication and Sleeve Gastrectomy
Transoral Fundoplication procedure completed prior to Sleeve Gastrectomy
Gastric Bypass
Laparoscopic Roux-en-Y gastric bypass

Locations

Country Name City State
United States Lexington Health Incorporated West Columbia South Carolina

Sponsors (1)

Lead Sponsor Collaborator
Lexington Health Incorporated

Country where clinical trial is conducted

United States, 

References & Publications (6)

Barr AC, Frelich MJ, Bosler ME, Goldblatt MI, Gould JC. GERD and acid reduction medication use following gastric bypass and sleeve gastrectomy. Surg Endosc. 2017 Jan;31(1):410-415. doi: 10.1007/s00464-016-4989-4. Epub 2016 Jun 10. — View Citation

DuPree CE, Blair K, Steele SR, Martin MJ. Laparoscopic sleeve gastrectomy in patients with preexisting gastroesophageal reflux disease : a national analysis. JAMA Surg. 2014 Apr;149(4):328-34. doi: 10.1001/jamasurg.2013.4323. — View Citation

Rondelli F, Bugiantella W, Vedovati MC, Mariani E, Balzarotti Canger RC, Federici S, Guerra A, Boni M. Laparoscopic gastric bypass versus laparoscopic sleeve gastrectomy: A retrospective multicenter comparison between early and long-term post-operative outcomes. Int J Surg. 2017 Jan;37:36-41. doi: 10.1016/j.ijsu.2016.11.106. Epub 2016 Nov 29. — View Citation

Tai CM, Huang CK. Increase in gastroesophageal reflux disease symptoms and erosive esophagitis 1 year after laparoscopic sleeve gastrectomy among obese adults. Surg Endosc. 2013 Oct;27(10):3937. doi: 10.1007/s00464-013-3022-4. Epub 2013 May 25. No abstract available. — View Citation

Testoni PA, Testoni S, Mazzoleni G, Vailati C, Passaretti S. Long-term efficacy of transoral incisionless fundoplication with Esophyx (Tif 2.0) and factors affecting outcomes in GERD patients followed for up to 6 years: a prospective single-center study. Surg Endosc. 2015 Sep;29(9):2770-80. doi: 10.1007/s00464-014-4008-6. Epub 2014 Dec 6. — View Citation

Trad KS, Turgeon DG, Deljkich E. Long-term outcomes after transoral incisionless fundoplication in patients with GERD and LPR symptoms. Surg Endosc. 2012 Mar;26(3):650-60. doi: 10.1007/s00464-011-1932-6. Epub 2011 Sep 30. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Measure change in reflux symptoms, impact of symptoms, and satisfaction of current status with the Gastroesophageal Reflux Disease Health Related Quality of Life (GERD HRQL-RSI) Questionnaire The GERD HRQL-RSI Questionnaire quantifies the symptoms of reflux the patient experiences, as well as the impact of symptoms on their daily life, and their satisfaction with their current status. The questionnaire also evaluates reflux medication use, which is another measure of treatment effectiveness. Items are rated on a scale of 0-5. The lowest possible score equals no symptoms. TS Cohort : Initial consultation, up to 6 weeks post fundoplication, up to 6 months post sleeve gastrectomy. RNY Cohort : At initial consultation, up to 6 months post RNY
Secondary Measure change in Body Mass Index (BMI) BMI is measured at initial consultation, up to 6 weeks post fundoplication, up to 6 months post LSG or RNY, and 12 months post LSG or RNY. It is a variable that may influence reflux symptoms. TS Cohort: Initial Consultation, up to 6 weeks post fundoplication, up to 6 months post sleeve gastrectomy, 12 months post LSG. For the RNY Cohort, Initial Consultation and up to 6 months post RNY and 12 month post RNY.
See also
  Status Clinical Trial Phase
Completed NCT02135107 - A Double-blind Comparative Study of the Efficacy and Safety of E3810 10mg Once and Twice Daily in Maintenance Therapy for PPI Resistant Gastroesophageal Reflux Disease Patients Phase 3
Completed NCT01432392 - Symptom Control and Impact on Daily Life in Patients With Gastroesophageal Reflux Disease N/A
Recruiting NCT01249482 - Symptom Assessment for GERD Patients Receiving H. Pylori Eradication N/A
Completed NCT01200550 - The Study to Describe Symptom Control and Impact on Daily Life in Gastroesophageal Reflux Disease (GERD) Patients N/A
Completed NCT01578642 - Feasibility Study for Evaluating the Effect of Electrical Stimulation on Lower Esophageal Sphincter Pressure and Esophageal Acid Exposure in Patients With Gastroesophageal Reflux Disease Phase 2
Completed NCT00998244 - Study to Evaluate the Effect of a Very Low Carbohydrate Diet on Gastroesophageal Reflux Disease N/A
Completed NCT00978016 - A Study to Evaluate the Efficacy and Safety of Arbaclofen Placarbil (XP19986) as Adjunctive Therapy in Subjects With Gastroesophageal Reflux Disease (GERD) Phase 2
Unknown status NCT01128608 - The Effect of High PCO2 Solution on Esophageal Acid Sensation N/A
Completed NCT00768196 - Prevalence of EED and Quality of Life Evaluated by Gastroesophageal Reflux Disease (GERD)-Q in Korean GERD Patients N/A
Completed NCT00768443 - Symptoms and Management Strategies in Gastroesophageal Reflux Disease (GERD) N/A
Recruiting NCT00498082 - Determinants of Efficacy of EsophyX Treatment in Gastro-Esophageal Reflux Disease N/A
Completed NCT00886197 - Diagnostic Efficacy of Narrow Band Imaging in Patients With Gastroesophageal Reflux Disease N/A
Completed NCT00378898 - Feasibility of Placing Bravo PH Capsule in Proximal Esophagus N/A
Completed NCT00507377 - Foreshortened Esophagus and Its Surgical Therapy
Completed NCT00217347 - Evaluation of Efficiency of Esophageal Capsule Endoscopy in the Screening of Patients With Gastroesophageal Reflux Disease or Dyspepsia as Compared to Upper Endoscopy N/A
Completed NCT00165022 - Development of a Novel Disease-Specific Quality of Life Questionnaire for Gastroesophageal Reflux Disease (GERD) Patients in Chinese Population N/A
Completed NCT00625495 - Study Comparing the Effects of Esomeprazole Adminstered Orally and Intravenously on Basal and Pentrigastrin-stimulated Acid Output in Subjects With Symptoms of Gastroesophageal Reflux Disease (GERD) Phase 4
Completed NCT00214552 - Evaluate the Effects on Asthma Control of Rabeprazole Given Twice Daily in Subjects With Asthma. Phase 3
Completed NCT00618150 - Patient Education in Gastroesophageal Reflux Disease N/A
Completed NCT03299985 - Diaphragmatic Myofascial Release in Gastroesophageal Reflux Disease N/A