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POP-UP: a Single-arm, Two-cohort Study: an 8-week Trimodal Pre-habilitation Program for Patients With Pancreatic Ductal Adenocarcinoma and Oesogastric

Study acronym: POP-UP
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary endpoint reworded 1 of 1 changed
See other at-risk trials from GERCOR - Multidisciplinary Oncology Cooperative Group

Record History

See every version on ClinicalTrials.gov ↗

  1. Notable Primary endpoint(s) modified Show 6 more changesShow less
    • Enrollment reopened
    • Enrollment increased: 9 → 72 participants
    • Study sites: 10 to 11
    • Eligibility criteria expanded, about 15 words
    • Secondary endpoints revised (29)
    • Study description expanded, about 3 words
  2. Notable Primary endpoint revisedv4 Show 7 more changesShow less
    • Trial status: Recruiting to Active, Not Recruiting
    • Enrollment target: estimated 72 to confirmed 9
    • Study sites: 4 to 10
    • Secondary endpoints: 16 to 29
    • Study description shortened, about 25 words
    • Eligibility criteria shortened, about 1 word
    • Study title expanded, about 5 words
  3. Notable Primary completion date: Mar 2027 to Dec 2027
    • Study completion date: Mar 2027 to Jun 2028
    • Start date changed from estimate of Aug 2024 to Jun 24, 2024
    v3
  4. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date: Mar 2024 to Aug 2024
    • Study sites: 0 to 4
    v2
  5. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This is a prospective, multicenter, two-cohort, open-label, single-arm feasibility study of a trimodal (nutritional, psychological, and personalized Adapted Physical Activity (APA)-individualized interventions) 8-week prehabilitation program in patients with localized pancreatic ductal adenocarcinoma (PDAC) or oesogastric cancer (OGC) receiving peri-operative triple chemotherapy and undergoing surgery.
Trial Details
NCT Number NCT06275737
Lead Sponsor GERCOR - Multidisciplinary Oncology Cooperative Group
Conditions
(from sponsor)
Pancreatic Ductal Adenocarcinoma, Esophageal Cancer
Related terms Esophageal Neoplasms
Enrollment 72 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov