Actively Recruiting
Endoscopic Conversion of Sleeve Gastrectomy to Single Anastomosis Sleeve-ileal Bypass (SASI) for Gastroesophageal Reflux (GERD), Primary and Secondary Non-responder.
Led by Singapore Health Services · Updated on 2025-02-14
500
Participants Needed
3
Research Sites
99 weeks
Total Duration
On this page
Sponsors
S
Singapore Health Services
Lead Sponsor
C
Changi General Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
The aim of this study is to determine the feasibility and effectiveness of endoscopic anastomosis of sleeve gastrectomy to ileum with a lumen apposing metal stent (LAMS) after a failed sleeve gastrectomy.
CONDITIONS
Official Title
Endoscopic Conversion of Sleeve Gastrectomy to Single Anastomosis Sleeve-ileal Bypass (SASI) for Gastroesophageal Reflux (GERD), Primary and Secondary Non-responder.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 21 and 65 years
- Patients scheduled for laparoscopic sleeve gastrectomy at participating hospitals
- Able to provide informed consent
You will not qualify if you...
- Currently pregnant or breastfeeding
- Severe psychiatric illness
- Eating disorder
- Active cancer
- End-stage kidney disease
- Bleeding disorders
- Presence of pacemaker or implantable cardiac defibrillator
- Significant heart diseases such as recent heart attack, heart failure, ischemic heart disease, irregular heart rhythms
- Factors likely to limit following the study protocol, including dementia, substance abuse, history of unreliability in medication or appointments, or concerns from family
- Treatment with anti-platelet medications that cannot be stopped temporarily
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
Changi General Hospital
Singapore, Singapore
Actively Recruiting
2
Sengkang General Hospital
Singapore, Singapore
Actively Recruiting
3
Singapore General Hospital
Singapore, Singapore
Actively Recruiting
Research Team
C
Chin Hong Lim, MD
CONTACT
W
Wei Min Chong, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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