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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05189574
Other study ID # EVac-LSGL
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 3, 2020
Est. completion date December 17, 2021

Study information

Verified date January 2022
Source Ruhr University of Bochum
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Endoscopic negative pressure therapy (ENPT) is a safe technique, showing promising results in the treatment of leakages of the upper and lower gastrointestinal tract. The purpose of this study is to determine the safety and efficacy of ENPT in the management of proximal staple line leak after sleeve gastrectomy.


Description:

Clinical data of 40 cases of post-SG proximal staple line leak treated with ENPT are analysed. Success is defined as resolution of the fistula with no further need for intervention (surgical or endoscopic).


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date December 17, 2021
Est. primary completion date June 30, 2021
Accepts healthy volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Staple line leak detected by endoscopy and/or CT within 30 days after surgery. - Age 18 years or older. - Written informed consent. Exclusion Criteria: - Declined informed consent. - Leaks detected later than 30 days after surgery.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Endoscopic negative pressure therapy
Endoscopic placement of a sponge in/at staple line leaks under negative pressure.

Locations

Country Name City State
Germany Klinikum Vest GmbH Recklinghausen NRW

Sponsors (1)

Lead Sponsor Collaborator
Ruhr University of Bochum

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of patients with closure of staple line leak Resolution of the fistula with no further need for intervention (surgical or endoscopic). up to 16 weeks
Secondary Number of endoscopic interventions Number of endoscopic interventions in each patient up to 16 weeks
Secondary Hospital stay Time of hospital stay for each patient up to 24 weeks
Secondary Mortality Mortality rate during hospital stay up to 24 weeks
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