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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: Recruiting Phase 4 study of Infertility, Female, sponsored by University of Southern California.

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. According to ClinicalTrials.gov, the official US trial registry.

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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.

Primary Outcome

The number of mature oocytes retrieved at oocyte retrieval

Conditions Studied

Interventions

  • DRUG Clomiphene Citrate

Study Locations (1)

California

  • HRC Fertility - Pasadena

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2025-06-01
Est. Completion 2027-12
Phase Phase 4
University of Southern California

617 total trials

What NCT06701071 shows while recruiting

NCT06701071 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, below the 376-participant average among 18 other Infertility, Female trials with a reported enrollment target (68% lower).

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 a single indexed study location in 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.

Similar trials for Infertility, Female

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06701071's enrollment target sits among peer trials

120 8th of 18 higher than 11 of 18 other Infertility, Female trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Infertility, Female trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06701071, the US trial registry maintained by the National Library of Medicine. NCT06701071 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.