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Benefit of GnRH Agonist Before Frozen Embryo Transfer in Patients With Endometriosis and/or Adenomyosis

Study acronym: DECATEC
StatusRecruiting
PhasePhase 2/3
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated January 16, 2026 (before its estimated June 18, 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Minor Re-verified, no change to tracked fieldsv11
  2. Notable Primary and study completion dates: Jun 18, 2025 to Jun 18, 2026v10
  3. Minor Re-verified, no change to tracked fieldsv9
  4. Notable Primary and study completion dates: Jan 1, 2023 to Jun 18, 2025v8
  5. Notable Primary and study completion dates: Jan 1, 2022 to Jan 1, 2023v7
Show 5 earlier versionsHide 5 earlier versions
  1. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    • Start date changed from estimate of Mar 30, 2021 to Mar 18, 2021
    v6
  2. Notable Phase: Phase 4 to Phase 2/3
    • Start date: Feb 15, 2021 to Mar 30, 2021
    v5
  3. Notable Start date: Nov 15, 2020 to Feb 15, 2021v4
  4. Notable Start date: Oct 1, 2020 to Nov 15, 2020v3
  5. Notable Start date: Jun 1, 2020 to Oct 1, 2020
    • Primary and study completion dates: Sep 1, 2021 to Jan 1, 2022
    v2
  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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Women suffering from endometriosis and/or adenomyosis may also suffer from infertility. GnRH agonist injection could improve implantation and therefore increase the pregnancy rate in these patients. This study was designed to evaluate effects of the additional of GnRH agonist (single or 2 doses) to the routine oestrogens and progestins use as support before Frozen Embryon Transfer as compared to oestrogens and progestins only.
Trial Details
NCT Number NCT04356664
Lead Sponsor Hopital Foch
Conditions
(from sponsor)
Endometriosis, Adenomyosis, Infertility, Female
Related terms Adenomyosis, Endometriosis, Infertility, Female
Enrollment 180 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov