Investigation of complications after bariatric surgery in the UK
A National Multi-centre Prospective Audit of Unplanned Surgical and Endoscopic Interventions in Patients Who Have Undergone Bariatric Surgery in the UK or Abroad
This study looks at the problems some people face after weight loss surgery in the UK to see how they are treated and what works best for their recovery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 500 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Bedfordshire Hospitals NHS Foundation Trust Academic / other |
| Locations | 1 site (Luton) |
| Trial ID | NCT06738004 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the incidence, management, and outcomes of complications following bariatric surgery in the United Kingdom. Patients presenting with complications will be identified from hospitals, and their data will be collected regarding demographics, surgical history, and treatment outcomes. The study will analyze different management strategies to determine their effectiveness and impact on patient outcomes, ultimately aiming to identify best practices for emergency bariatric care.
Who should consider this trial
Good fit: Ideal candidates for this study are patients who have undergone bariatric surgery and are presenting with complications requiring unplanned interventions.
Not a fit: Patients under 18 years old or those whose complications are unrelated to previous bariatric surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved management strategies and outcomes for patients experiencing complications after bariatric surgery.
How similar studies have performed: While similar studies have been conducted, this specific observational approach focusing on emergency complications in bariatric surgery is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Admissions from i) the emergency department, clinic, urgent care or primary care to the bariatric surgical team as an emergency; ii) from an inpatient team as an urgent referral; iii) a return to theatre following an elective bariatric procedure; iv) another hospital via patient transfer to a specialised unit. * Participants undergoing any intervention or procedure to treat or diagnose bariatric complications, (e.g., OGDs, interventional radiology, surgery, supplemental enteral or parenteral nutrition). Exclusion Criteria: * age \<18 years old * have a length of stay \<24 hrs. * initial diagnosis of BSE is changed or if their readmission is found to be unrelated to previous bariatric surgery.
Where this trial is running
Luton
- Luton and Dunstable Hospital — Luton, United Kingdom (Recruiting)
Study contacts
- Principal investigator: Mohamed Aly, FRCS — The Hillingdon Hospitals NHS Foundation Trust
- Study coordinator: Mohamed Aly, FRCS
- Email: m.aly@nhs.net
- Phone: 01895 279994
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.