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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03890354
Other study ID # 2018/1006
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 21, 2019
Est. completion date April 15, 2019

Study information

Verified date April 2019
Source Mahidol University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

There are a lot of surgical techniques in minimally-invasive surgery to remove gastric subepithelium tumor. Surgical approach depend on location and size of tumor. Usefully used Endostapler to cut stomach include lesion. For tumors in difficult locations some surgeons prefer laparoscopic and endoscopic cooperation or use the intragastric port technique to identify and remove the mass. But in complex procedures, gastotomy and hand sawn to identify and remove gastric subepithelium tumor is a simple technique and easy to apply. This study demonstrates the safety and effectiveness of this technique.


Description:

: A retrospective chart review was made of all patients who presented with gastric subepithelial tumor and underwent laparoscopic or robotic resection at Ramathibodi Hospital during 2012-2018. Surgical outcomes and complication of gastotomy and hand-sewn repair were analyzed.


Recruitment information / eligibility

Status Completed
Enrollment 27
Est. completion date April 15, 2019
Est. primary completion date March 30, 2019
Accepts healthy volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- all patients who presented with gastric subepithelial tumor and underwent laparoscopic or robotic resection at Ramathibodi Hospital during 2012-2018.

Exclusion Criteria:

- conversion to open surgery

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Hand-Sewn Repair
gastotomy to identify and remove gastric subepithelium tumor and hand sawn repair

Locations

Country Name City State
Thailand Chairat Supsamutchai Bangkok Bankok

Sponsors (1)

Lead Sponsor Collaborator
Mahidol University

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Post operative complication anastomosis leak 7 day
Primary Post operative compliction wound infection 7 day
Secondary Surgical outcome Complete remove mass with out rupture 7 day