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Truncal Vagotomy in Patients Undergoing Revisional Sleeve Gastrectomy to Gastric Bypass

Truncal Vagotomy in Patients Undergoing Revisional Sleeve Gastrectomy to Gastric Bypass

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04901429
Enrollment
200
Registered
2021-05-25
Start date
2021-07-01
Completion date
2028-08-01
Last updated
2025-05-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

GERD

Brief summary

The purpose of this study is to investigate the efficacy of performing a truncal vagotomy along with a sleeve to bypass revision surgery in reducing the severity and/or incidence of gastroesophageal reflux disease (GERD) post-surgery.

Interventions

PROCEDURETruncal vagotomy

Truncal vagotomy will be performed in 50% of patients during other routine procedure.

Sponsors

Baylor Research Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Participating subjects will need to be \>18yrs of age and eligible for sleeve to bypass revision bariatric surgery. * Undergoing sleeve to bypass revision bariatric surgery.

Exclusion criteria

* Patients who are under the age of 18. * Not eligible for sleeve to bypass revision bariatric surgery.

Design outcomes

Primary

MeasureTime frameDescription
GERD-HRQL scoresapproximately 6 months post operationGERD-HRQL scores
Esophageal pH monitoringapproximately 6 months post operationEsophageal pH monitoring
Reflux symptom index questionnaireapproximately 6 months post operationReflux symptom index questionnaire

Countries

United States

Contacts

Primary ContactResearch Project Coordinator
ADVANCEDSURGERYRESEARCH@bswhealth.org214-820-4787

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026