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A Study of Minimally Invasive Proximal Gastrectomy Versus Minimally Invasive Total Gastrectomy for Gastric and Gastroesophageal Junction Cancers

Memorial Sloan Kettering Cancer Center (MSK) logo

Memorial Sloan Kettering Cancer Center (MSK)

Status

Active, not recruiting

Conditions

Gastric Cancer
GastroEsophageal Cancer
Gastroesophageal Junction Adenocarcinoma

Treatments

Other: MDASI-GI

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Participants will a diagnosis of gastroesophageal junction (GEJ) adenocarcinoma and will have either a minimally invasive proximal gastrectomy (MIPG) or a minimally invasive total gastrectomy (MITG) as part of their routine care. Participants with complete a questionnaire 1 month before the surgical procedure and then 1, 3, 6 and 12 months after the surgical procedure.

Enrollment

4 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Able to speak and read English, Spanish, Japanese or Korean
  • Patients with a biopsy-confirmed diagnosis of non-metastatic gastric or GEJ adenocarcinoma, who are scheduled to undergo MIPG or MITG for curative-intention
  • Age ≥ 18

Exclusion criteria

  • Patients with known malabsorption syndromes or a lack of physical integrity of the upper gastrointestinal tract
  • Patients with known narcotic dependence, with average daily dose > 5 mg oral morphine equivalent
  • Subjects deemed unable to comply with study and/or follow-up procedures, at investigators' discretion
  • Patients who are pregnant (since are excluded from receiving standard-of-care MIPG or MITG)

Trial design

4 participants in 2 patient groups

Minimally Invasive Proximal Gastrectomy/MIPG
Description:
Participants will undergo MIPG (Trial Procedure)
Treatment:
Other: MDASI-GI
Minimally Invasive Total Gastrectomy/MITG
Description:
Participants will undergo MITG (Standard of Care/Control Group)
Treatment:
Other: MDASI-GI

Trial contacts and locations

8

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Central trial contact

Vivian Strong, MD; Daniel Coit, MD

Data sourced from clinicaltrials.gov

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