Trans-Pacific Multicenter Collaborative Study of Minimally Invasive Proximal Versus Total Gastrectomy for Proximal Gastric and Gastroesophageal Junction Cancers
Condition(s) studied
Investigational drug(s) / intervention(s)
Standard of Care: complete a questionnaire within 30 days before your surgery and then at 1, 3, 6, and 12 months after surgery
Control Group: complete a questionnaire within 30 days before your surgery and then at 1, 3, 6, and 12 months after surgery
Study summary
To compare the symptoms of patients who have a MIPG to the symptoms of patients who have a MITG.
Eligibility
Primary outcome measure(s)
- (MDASI-GI) MD Anderson Symptom Inventory Questionnaire — 3 months after surgery
Appetite level (reported on a 0-10 scale, in Q8 of MDASI-GI) scale 0-not present-10 as bad as you can image
Trial sites (4)
| Facility | City | Region | Status |
|---|---|---|---|
| Mayo Clinic in Rochester | Rochester | Minnesota | Active Not Recruiting |
| M D Anderson Cancer Center | Houston | Texas | Recruiting |
| Keio University School of Medicine | Tokyo | Japan | Recruiting |
| Yonsei University College of Medicine | Soeul | South Korea | Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05205343 on ClinicalTrials.gov ↗ ← All trials in South Korea