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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04172545
Other study ID # 2020OSstaplingcondition
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date August 2020
Est. completion date December 2021

Study information

Verified date March 2020
Source AZ Sint-Jan AV
Contact Jan Paul Mulier, MD PhD
Phone +3250452490
Email jan.mulier@azsintjan.be
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Measure anesthetic condition used during laparoscopic sleeve gastrectomy stapling. Measure quality of stapling in resected stomach by measuring staple thickness. Find if any relation exists.


Description:

During each staple firing the staple size, time of compression and anesthetic conditions being systolic arterial pressure, fluids transfused and intra abdominal pressure used are recorded.

After removal of stapled stomach during surgery, thickness of stomach wall and thickness of staple line are measured and compared to evaluate quality of staple formation.

the closer the staple height to the wall thickness the better the quality of stapling. Because no one has ever analyzed this relationship, and certainly not under different anesthetic conditions it is not clear yet if any relationship will be found.

the analysis will help to understand the relation and help to start perhaps a randomised trial to learn what conditions are best to improve staple quality.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 10
Est. completion date December 2021
Est. primary completion date December 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- primary sleeve gastrectomy

Exclusion Criteria:

- stomach disease

- prior surgery on the stomach

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
stapling
staples are fired through the gastric wall after waiting several seconds for compression without attention to blood pressure, fluids given or intra abdominal pressure, but these might have an impact on quality of stapling. therefore the conditions during stapling will be recorded during stapling.

Locations

Country Name City State
Belgium Azsintjan Brugge

Sponsors (1)

Lead Sponsor Collaborator
AZ Sint-Jan AV

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary thickness of staple line thickness of staple line measured in micrometers intra operative on excised stomach before being discarded
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