Transoral Removal of Specimen During Laparoscopic Gastric Resection

Investigators aimed to present the patients who underwent laparoscopic gastrectomy with transoral specimen extraction.

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Key information

Conditions

Gastric Disease Bariatric Surgery Candidate Digestive System Diseases Gastrointestinal Diseases Stomach Diseases

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Cihan Gokler

Malatya, 44090, Turkey (Türkiye)

About this study

Minimally invasive surgical procedures such as NOSE (Natural orifice spesmen extraction) and NOTES (Natural orifice translumenal endoscopic surgery) are gradually increasing. The transoral way is probably the least used for NOSE.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

laparoscopic gastric resection
Patients aged 18-70 years

Exclusion criteria

other transorally removed organs (appendix, gallbladder, surrenal)

Treatment and study plan

transoral specimen extraction

Procedure

transoral specimen extraction during laparoscopic gastric resection

Other names: laparoscopic gastric resection

Primary outcomes

Transoral Specimen Extraction During Laparoscopic Gastric Resection

Time frame: 2 years

laparoscopic gastric resections due to sleeve gastrectomy or pyloric obstruction will be observed after transoral removal.

Sponsors and collaborators

Lead sponsor

Inonu University

Other

Registry information

Important dates

Study start: 2019
Primary completion: 2019
Study completion: 2019
First posted: Oct 1, 2019
Registry last updated: Oct 1, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed