Recruiting NCT05257434
Postoperative Outcomes in Patients With Hepato-biliary-pancreatic Cancer According to inBody Test
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: inbody.
- Who it may be relevant to
- Registry conditions: Cancer. Basic parameters: 18 years — 90 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Japan
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
postoperative outcomes were evaluated by using inBody test
Detailed description
postoperative outcomes were evaluated by using inBody test
Interventions
- Behavioral inbody
Body fluid composition
Primary outcome measures
- long-term outcomes [Time frame: 5year]
Secondary outcome measures (1)
- short-term outcomes [Time frame: up to 24 weeks]
Eligibility criteria
Inclusion criteria
- surgically treated patients
Exclusion criteria
- a body weight loss of >10% during the 6 months before surgery; the presence of distant metastases; or seriously impaired function of vital organs because of respiratory, renal, or heart disease
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Japan · 1 center
- Takehiro Okabayashi — Kochi
Publications
- Kimura J, Sui K, Tabuchi M, Sakamoto S, Murokawa T, Iwata J, Morita S, Iiyama T, Okabayashi T. Preoperative percent body fat in bioelectrical impedance analysis predicts pancreatic fistula after pancreaticoduodenectomy. Langenbecks Arch Surg. 2023 Jun 28;408(1):248. doi: 10.1007/s00423-023-02998-y. PMID 37380749
Identifiers
NCT: NCT05257434 · Point study