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Truncal Vagotomy in Patients Undergoing Revisional Sleeve Gastrectomy to Gastric Bypass

Baylor Scott and White Health (BSWH) logo

Baylor Scott and White Health (BSWH)

Status

Enrolling

Conditions

GERD

Treatments

Procedure: Truncal vagotomy

Study type

Interventional

Funder types

Other

Identifiers

NCT04901429
021-171

Details and patient eligibility

About

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.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

200 participants in 2 patient groups

Truncal Vagotomy
Experimental group
Description:
Truncal vagotomy will be performed during other routine procedure.
Treatment:
Procedure: Truncal vagotomy
No Truncal Vagotomy
No Intervention group
Description:
No truncal vagotomy will be performed during other routine procedure.

Trial contacts and locations

1

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Central trial contact

Research Project Coordinator

Data sourced from clinicaltrials.gov

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