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TC or BEP in Treating Patients With Ovarian Malignant Sex Cord-Stromal Tumors

Study acronym: SCST-01
StatusRecruiting
PhasePhase 3
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated April 25, 2023 (before its estimated May 2025 completion). Its status may not reflect the trial's current state.

Record History

See every version on ClinicalTrials.gov ↗

  1. Minor Re-verified, no change to tracked fieldsv8
  2. Notable Primary completion date: May 2021 to May 2025
    • Study completion date: May 2024 to May 2030
    v7
  3. Minor Re-verified, no change to tracked fieldsv6
  4. Minor Study description expanded, about 2 wordsv5
  5. Notable Primary completion date: May 2018 to May 2021
    • Trial status: Enrolling by Invitation to Recruiting
    • Study completion date: May 2020 to May 2024
    • Site details revised
    v4
Show 2 earlier versionsHide 2 earlier versions
  1. Notable Trial status: Active, Not Recruiting to Enrolling by Invitation
    • Eligibility criteria revised
    v3
  2. Minor Re-verified, no change to tracked fieldsv2
  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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
1,336 trials monitored
See 90 trials at risk
Investigators will conduct the trial to determine whether paclitaxel and cisplatin (PT) has the same curative effects and less adverse effects than bleomycin, etoposide and cisplatin(BEP) among newly diagnosed ovarian malignant sex cord-stromal tumor patients after surgery.
Trial Details
NCT Number NCT02429700
Lead Sponsor Beihua Kong
Collaborators: Huazhong University of Science and Technology, Zhejiang University, Sun Yat-sen University
Conditions
(from sponsor)
Ovarian Sex Cord Stromal Tumor, Ovarian Neoplasms, Ovarian Cancer
Related terms Ovarian Neoplasms
Enrollment 132 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov