Actively Recruiting
LINX vs Fundoplication
Led by University of Oxford · Updated on 2025-08-05
460
Participants Needed
5
Research Sites
225 weeks
Total Duration
On this page
Sponsors
U
University of Oxford
Lead Sponsor
K
King's College London
Collaborating Sponsor
AI-Summary
What this Trial Is About
Reflux disease can severely impact upon quality-of-life and lead to complications, including ulceration of the oesophagus. It is often controlled with self-help measures and medication. However, sometimes surgery is recommended. The current standard surgical treatment is called a fundoplication. This operation is carried out through keyhole (laparoscopic) surgery, and tightens the lower oesophagus to prevent reflux. Fundoplication is very safe and improves the quality-of-life of most patients. However, many patients have gas bloating, difficulty swallowing and recurrence of their reflux symptoms. As an alternative, some surgeons use a device called LINX, using a keyhole procedure. LINX is a magnetic device that wraps around the lower oesophagus to prevent reflux. Studies suggest that LINX may cause fewer complications, with a similar improvement in quality-of-life. However, there is a need for better evidence to compare LINX with fundoplication in the surgical treatment of reflux disease. GOLF is a multi-centre study designed which to determine if LINX achieves similar reflux control and improves symptoms compared to fundoplication. GOLF measures: (1) quality of life,(2) surgical complications, including need for additional treatment, (3) financial cost-effectiveness and (4) objectively measure the presence of acid that has refluxed into the lower oesophagus. GOLF aims randomise 460 patients to receive fundoplication or the LINX device. It will be conducted across at least 16 UK and 7 European specialist surgical centres. All participants will be followed up at 6 weeks, 6, 12 and 24 months to assess which treatment offers the best results after surgery. A quality assurance programme within participating centres will ensure that procedures are completed to a high-quality standard. Study results will incorporate a patient and public involvement programme, which will inform national and international guidelines for the surgical treatment of reflux disease.
CONDITIONS
Official Title
LINX vs Fundoplication
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years and above
- Willing and able to give informed consent
- Patients with GORD not adequately controlled by medication or intolerant to medication, considered for anti-reflux surgery
- Symptomatic and objectively confirmed GORD by endoscopy or 24-hour pH or BRAVO test
- No hiatal hernia or hiatal hernia less than 5 cm in length
- Adequate lower oesophageal motility shown by manometry with mean contractile amplitude greater than 30 mmHg or DCI greater than 450 mmHg-s-cm in 70% of swallows
You will not qualify if you...
- Unsuitable for surgery due to medical conditions preventing general anaesthesia
- Known or suspected allergies to titanium, stainless steel, nickel, or ferrous materials
- Previous anti-reflux or gastric surgery
- Previous or planned neurosurgical intervention
- Complete absence of lower oesophageal contractility on manometry
AI-Screening
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Trial Site Locations
Total: 5 locations
1
Guy's and St Thomas's NHS Foundation Trust, Guy's and St Thomas's Hospital
Oxford, Oxfordshire, United Kingdom, OX3 7LD
Actively Recruiting
2
Imperial College Healthcare NHS Trust, St Mary's Hospital
Oxford, Oxfordshire, United Kingdom, OX3 7LD
Actively Recruiting
3
Leeds Teaching Hospitals NHS Trust, St James's University Hospital
Oxford, Oxfordshire, United Kingdom, OX3 7LD
Actively Recruiting
4
Oxford University Hospitals NHS Foundation Trust, Churchill Hospital
Oxford, Oxfordshire, United Kingdom, OX3 7LD
Actively Recruiting
5
University Hospital Southampton NHS Foundation Trust
Oxford, Oxfordshire, United Kingdom, OX3 7LD
Actively Recruiting
Research Team
S
Sheraz Markar, PhD, FRCS, MSc, MA
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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