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NCT06701071 · ClinicalTrials.gov registry record · Phase 4
Evaluation of a Long Versus Short Clomid Protocol for Controlled Ovarian Stimulation
A Phase 4 study of Infertility, Female, sponsored by University of Southern California.
- Recruiting
- Registry status
- Phase 4
- Development phase
- 120
- Enrollment target
- 1
- Study location
NCT06701071 is a Phase 4 study of Infertility, Female that is actively recruiting participants, run by University of Southern California. The registered enrollment target is 120 participants, below the 376-participant average among 18 other Infertility, Female trials with a reported enrollment target (68% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06701071, a Phase 4 study of Infertility, Female, is actively recruiting participants, sponsored by University of Southern California.
- RECRUITING
- Registry status
- Phase 4
- Development phase
- 120 participants
- Enrollment target
- 1
- Study location
Study Summary
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.
Conditions Studied
Interventions
- DRUG Clomiphene Citrate
Study Locations (1)
California
- HRC Fertility - Pasadena
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2025-06-01 |
| Est. Completion | 2027-12 |
| Phase | Phase 4 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06701071
The ClinicalTrials.gov registry entry for NCT06701071 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 376-participant average among 18 other Infertility, Female trials with a reported enrollment target (68% lower). The listed sponsor is University of Southern California, which has 617 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Infertility, Female appearing as the primary indexed condition, and to 1 intervention - of which Clomiphene Citrate is the first listed.
NCT06701071 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT06701071 about?
NCT06701071 is a clinical study titled "Evaluation of a Long Versus Short Clomid Protocol for Controlled Ovarian Stimulation". 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 ...
What is the current status of trial NCT06701071?
This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 120 participants. The study started on 2025-06-01. Estimated completion is 2027-12.
What conditions does trial NCT06701071 study?
This clinical trial studies the following conditions: Infertility, Female.
What interventions are being tested in trial NCT06701071?
The interventions under investigation include: Clomiphene Citrate (DRUG).
Who is sponsoring clinical trial NCT06701071?
This trial is sponsored by University of Southern California, which has 617 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06701071 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.