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Phase II trial to evaluate compliance of postoperative nutrition by Uplead in total gastrectomy for gastric cancer

Phase II trial to evaluate compliance of postoperative nutrition by Uplead in total gastrectomy for gastric cancer - Uplead trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000032291
Enrollment
35
Registered
2018-04-17
Start date
2018-02-16
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastric cancer

Interventions

Supplementation of Uplead

Sponsors

Kanagawa Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: i. Histologically proven adenocarcinoma of the stomach ii.Clinical T1-T4a and no distant metastasis iii.R0 resection is possible by open total gastrectomy iv.Enough oral intake after sugery v.Age ranging between 20 and more. vi.ECOG performance status 0-1. vii.Not cancer of the remnant stomach viii.Suficient organ functions. iv.Written informed consent.

Exclusion criteria

Exclusion criteria: i.Synchronous or metachronous cancer (synchronous multiple cancers in the stomach included). ii.Active inflammation which requires systemic treatment iii.Allergy for contents of Uplead iv.Uncontrollable diabetes mellitus v.Systemic treatment with corticosteroid vi.Unstable angina or cardiac infarction within 6 months vii.Pulmonary disorder under oxygen viii.Woman with on-going pregnancy or breast-feeding, or contemplating pregnancy. ix.Mental disorders which may affect ability or willingness to provide informed consent or abide by the study protocol

Design outcomes

Primary

MeasureTime frame
compliance with supplementation

Secondary

MeasureTime frame
body weight and lean body mass reduction 1 month and 3 months after surgery

Countries

Japan

Contacts

Public ContactTakanobu Yamada

Kanagawa Cancer Center Department of Gastrointestinal Surgery

tknbymd@kcch.jp+81-45-520-2222

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026