Comparison of Tumor Efficacy Safety in Laparoscopic Resection of Gastrointestinal Stromal Tumors Between Favorable and Unfavorable Site

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorFujian Medical University

About this trial

Participants with gastrointestinal stromal tumors(GIST) were divided into favorable and unfavorable sites according to the anatomical site of the tumor, and this study aims to validate the overall postoperative morbidity and mortality rates between favorable site receiving laparoscopic resection of GIST and that of unfavorable site under the currently standard surgical therapy.

Eligibility criteria

Qualifiers

Age between 18 and 75 years old

Primary gastric lesion confirmed pathologically GIST by endoscopic biopsy. Preoperative endoscopy, ultrasound endoscopy or computer tomography, Magnetic resonance suspected GIST, and then postoperative pathology confirmed as the original GIST

Written informed consent

Expected R0 resection by laparoscopy

Disqualifiers

Pregnant and lactating women

Suffering from a severe mental disorder

History of previous upper abdominal surgery (except for laparoscopic cholecystectomy)

History of previous gastric surgery (including ESD/EMR for gastric cancer)

Trial design

Treatments tested in this trial

  • Laparoscopic resection

Treatment groups

250 Participants
are divided into 2 treatment groups

Sponsors and collaborators