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Prophylactic Pyloric Balloon Dilatation During Ivor Lewis Oesophagectomy

NCT05085951 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2023-11-18

No results posted yet for this study

Summary

This is a feasibility study to assess recruitment for a randomised control trial comparing prophylactic pyloric ballon dilatation versus control group (no intervention) in Ivor-Lewis Oesophagectomy

Conditions

  • Postprocedural Delayed Gastric Emptying

Interventions

DEVICE

20 mm CRE balloon

Endoscopic balloon that is used to dilate pylorus

DIAGNOSTIC_TEST

OGD

OGD (No dilatation)

Sponsors & Collaborators

  • University Hospital Plymouth NHS Trust

    lead OTHER

Principal Investigators

  • Christopher Rollinson · University Hospitals Plymouth NHS Trust

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-12-09
Primary Completion
2022-08-31
Completion
2023-06-30

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05085951 on ClinicalTrials.gov