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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
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Reflux, Gastroesophageal

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    August 30, 2018
    Last Updated
    October 26, 2018
    Sponsor
    Karolinska Institutet
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    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

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    Comparison of Total and Partial Fundoplication During Surgery of Patients With Gastroesophageal Reflux Disease

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