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Evaluation of a Long Versus Short Clomid Protocol for Controlled Ovarian Stimulation

StatusRecruiting
PhasePhase 4
Started
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Record History

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  1. Study description expanded, about 36 words
    • Site contact updated
    v4
  2. Primary completion date: Mar 2026 to Jun 2028
    • Study completion date: Dec 2027 to Jun 2028
    v3
  3. Trial status: Not Yet Recruiting to Recruitingv2 Show 5 more changesShow less
    • Enrollment target: 60 to 120
    • Start date changed from estimate of Dec 2024 to Jun 1, 2025
    • Primary completion date: Sep 2025 to Mar 2026
    • Eligibility criteria expanded, about 47 words
    • Site details revised
  4. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 goal of this clinical trial is to evaluate a long Clomid protocol as compared to a 5-day Clomid protocol for ovarian stimulation in patients with diminished ovarian reserve undergoing ovarian stimulation for in-vitro fertilization. The aim of the long Clomid protocol is to intensify stimulation of the ovaries and reduce both cost and injection burden for patients. Participants will be randomized to receive the long Clomid protocol vs. the typical protocol involving Clomid only for 5 days followed by growth hormone-releasing hormone (GnRH) antagonist. The primary outcome the investigators will evaluate will be the number of mature eggs retrieved.
Trial Details
NCT Number NCT06701071
Lead Sponsor University of Southern California
Conditions
(from sponsor)		 Infertility, Female
Related terms Infertility, Female
Enrollment 120 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov