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Palliative Radiation for Advanced Cervical Cancer

Study acronym: RAPPAL
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated February 17, 2026 (before its estimated July 1, 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Minor Re-verified, no change to tracked fieldsv10
  2. Notable Primary completion date: Jan 1, 2026 to Jul 1, 2026 Completion date: Jan 1, 2026 to Aug 1, 2026v9 Show 1 more changeShow less
    • Completion date: Jan 1, 2026 to Aug 1, 2026
  3. Notable Primary completion date: Aug 1, 2024 to Jan 1, 2026 Completion date: Feb 1, 2025 to Jan 1, 2026v8 Show 1 more changeShow less
    • Completion date: Feb 1, 2025 to Jan 1, 2026
  4. Minor Re-verified, no change to tracked fieldsv7
  5. Notable Phase: Phase 3 to Not applicablev6
Show 4 earlier versionsHide 4 earlier versions
  1. Minor 2 versions Re-verified since Sep 2, 2020, no change to tracked fieldsv4-v5
  2. Notable Trial status: Not Yet Recruiting to Recruiting Start date changed from estimate of May 1, 2020 to Jun 19, 2020 · Site details revisedv3 Show 2 more changesShow less
    • Start date changed from estimate of May 1, 2020 to Jun 19, 2020
    • Site details revised
  3. Notable Start date: Aug 1, 2019 to May 1, 2020 Collaborator revisedv2 Show 1 more changeShow less
  1. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
The present study is proposed to compare a rapid fractionation schedule of 1 week compared to a protracted schedule of 6-8 weeks for palliation for locally advanced cervical cancer.
Trial Details
NCT Number NCT03997110
Lead Sponsor Tata Memorial Hospital
Collaborators: Tata Memorial Centre
Conditions Cervical Cancer
Enrollment 230 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov