Comparison of Total and Partial Fundoplication During Surgery of Patients With Gastroesophageal Reflux Disease (RefluxII)
Primary Purpose
Reflux, Gastroesophageal
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Nissen
Toupét
Sponsored by
About this trial
This is an interventional treatment trial for Reflux, Gastroesophageal
Eligibility Criteria
Inclusion Criteria:
- surgery treatment for GERD
- laparoscopic surgery
Exclusion Criteria:
- previous surgery for GERD
- ASA classification >3
- paraesophageal hernias or large hiatal
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Nissen
Toupét
Arm Description
Surgery of GERD with 360 degrees total fundoplication
Surgery of GERD with 270 degrees partial fundoplication
Outcomes
Primary Outcome Measures
Esophageal acid exposure
24-hour pH measurement
Secondary Outcome Measures
Recurrens rates
Medical journal or patients description
Dysphagia scoring
Dysphagia for liquids and solids were recorded within a four-graded scale stating the frequency of dysphagia episodes with an arbitrary (empirical) cut off for clinical significance. The same dysphagia scoring was also used in a previous rct, from the same institution, comparing different types of antireflux procedures in open surgery.
Full Information
NCT ID
NCT03659487
First Posted
August 30, 2018
Last Updated
October 26, 2018
Sponsor
Karolinska Institutet
1. Study Identification
Unique Protocol Identification Number
NCT03659487
Brief Title
Comparison of Total and Partial Fundoplication During Surgery of Patients With Gastroesophageal Reflux Disease
Acronym
RefluxII
Official Title
Comparison of Total and Partial Fundoplication During Surgery of Patients With Gastroesophageal Reflux Disease
Study Type
Interventional
2. Study Status
Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
November 2001 (Actual)
Primary Completion Date
April 2011 (Actual)
Study Completion Date
October 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
460 patients who are scheduled for surgical treatment of gastroesophageal reflux disease (GERD) participate in the study following the usual preoperative Clinical routines (Medical history, endoscopy with biopsies, esophageal manometry with 24 hour pH (acidity) registration ). Patients are randomized to fundoplication according to Nissen or modified Toupet. Postoperatively, patients are monitored after 6 weeks 12, 36, 24 and 60 months.
Detailed Description
Patients aged 18-75 years planned for elective surgical treatment of GERD participate in the study. Patients with recurrent reflux disease following prior surgery, ASA (American Society of Anesthesiologists (ASA) Physical Status") class> 3, paraesophageal herniating and / or major herniation without reflux and those with other contraindications against laparoscopic surgery are excluded. In addition, patient completes a QOL protocol. Patients in the study are randomized to laparoscopic fundoplication performed either with a 360 degrees (Nissen) alternatively 270 degree (modified Toupét). Both of these techniques are well established clinical routines. General intubation anesthesia is standardized to all study patients. Discharge from the hospital is typically on the first postoperative day. At a visit, after 6-8 weeks for clinical control, is a QOL protocol is completed as well. After 12 and 36 months, patients undergo upper endoscopy and manometry with 24 hour pH-registration and QOL protocol completion. The latter also occurs after 24 months and 60 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Reflux, Gastroesophageal
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Laparoscopic total (Nissen) vs posterior 270 degrees (Toupét) partial fundoplication for the treatment of gastroesophageal reflux disease.
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
460 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Nissen
Arm Type
Active Comparator
Arm Description
Surgery of GERD with 360 degrees total fundoplication
Arm Title
Toupét
Arm Type
Active Comparator
Arm Description
Surgery of GERD with 270 degrees partial fundoplication
Intervention Type
Procedure
Intervention Name(s)
Nissen
Intervention Description
Laparoscopic total (Nissen) fundoplication
Intervention Type
Procedure
Intervention Name(s)
Toupét
Intervention Description
Laparoscopic posterior 270 degrees partial fundoplication
Primary Outcome Measure Information:
Title
Esophageal acid exposure
Description
24-hour pH measurement
Time Frame
Change from baseline at 6 weeks, 12 and 36 month
Secondary Outcome Measure Information:
Title
Recurrens rates
Description
Medical journal or patients description
Time Frame
Change from baseline at 6 weeks, 12, 36 and 60 month
Title
Dysphagia scoring
Description
Dysphagia for liquids and solids were recorded within a four-graded scale stating the frequency of dysphagia episodes with an arbitrary (empirical) cut off for clinical significance. The same dysphagia scoring was also used in a previous rct, from the same institution, comparing different types of antireflux procedures in open surgery.
Time Frame
Change from baseline at 6 weeks, 12, 36 and 60 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
surgery treatment for GERD
laparoscopic surgery
Exclusion Criteria:
previous surgery for GERD
ASA classification >3
paraesophageal hernias or large hiatal
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anders Thorell, professor
Organizational Affiliation
Karolinska Institut
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
30840057
Citation
Hakanson BS, Lundell L, Bylund A, Thorell A. Comparison of Laparoscopic 270 degrees Posterior Partial Fundoplication vs Total Fundoplication for the Treatment of Gastroesophageal Reflux Disease: A Randomized Clinical Trial. JAMA Surg. 2019 Jun 1;154(6):479-486. doi: 10.1001/jamasurg.2019.0047.
Results Reference
derived
Learn more about this trial
Comparison of Total and Partial Fundoplication During Surgery of Patients With Gastroesophageal Reflux Disease
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