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NCT06394752 · ClinicalTrials.gov registry record · NA
UTERINE EVALUATION FOR THE IDENTIFICATION OF PATHOLOGY. This Study Will Compare the Intrauterine Pathology Detection Rate Between Standard of Care Hydrosonography, and a New Visual Saline Infusion Device Providing Direct Visualization of the Uterus.
A NA study of Infertility, Female and Fertility Issues, sponsored by Center for Reproductive Health & Gynecology.
- Recruiting
- Registry status
- NA
- Development phase
- 100
- Enrollment target
- 2
- Study locations
NCT06394752: Recruiting NA study of Infertility, Female and Fertility Issues, sponsored by Center for Reproductive Health & Gynecology.
NCT06394752 is a NA study of Infertility, Female and Fertility Issues that is actively recruiting participants, run by Center for Reproductive Health & Gynecology. The registered enrollment target is 100 participants, below the 377-participant average among 18 other Infertility, Female trials with a reported enrollment target (73% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06394752, a NA study of Infertility, Female and Fertility Issues, is actively recruiting participants, sponsored by Center for Reproductive Health & Gynecology.
- RECRUITING
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
- 2
- Study locations
Study Summary
This is a prospective, single center, multiple arm cohort study intended to compare the diagnostic accuracy of a Visual Saline Infusion Device (VSI) device, vs standard of care Hydrosonography in reproductive aged women to identify pathology in the uterus.
Conditions Studied
Interventions
- DEVICE Visual Saline Infusion
- DEVICE Hydrosonography
Study Locations (2)
California
- Center for Reproductive Health & Gynecology - Beverly Hills
Nayarit
- Punta Mita Fertility Center - Corral Del Risco
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2024-04-25 |
| Est. Completion | 2025-07-30 |
| Phase | NA |
What NCT06394752 shows while recruiting
NCT06394752 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 377-participant average among 18 other Infertility, Female trials with a reported enrollment target (73% lower).
The record links to 7 conditions, with Infertility, Female appearing as the primary indexed condition, and to 2 interventions - of which Visual Saline Infusion is the first listed.
NCT06394752 reports a single indexed study location in California, Nayarit.
Frequently Asked Questions
What is clinical trial NCT06394752 about?
NCT06394752 is a clinical study titled "UTERINE EVALUATION FOR THE IDENTIFICATION OF PATHOLOGY. This Study Will Compare the Intrauterine Pathology Detection Rate Between Standard of Care Hydrosonography, and a New Visual Saline Infusion Device Providing Direct Visualization of the Uterus.". This is a prospective, single center, multiple arm cohort study intended to compare the diagnostic accuracy of a Visual Saline Infusion Device (VSI) device, vs standard of care Hydrosonography in reproductive aged women to identify pathology in the uterus.
What is the current status of trial NCT06394752?
This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2024-04-25. Estimated completion is 2025-07-30.
What conditions does trial NCT06394752 study?
This clinical trial studies the following conditions: Infertility, Female, Fertility Issues, Gynecology, Hysteroscopy, Hysteroscopy Technique.
What interventions are being tested in trial NCT06394752?
The interventions under investigation include: Visual Saline Infusion (DEVICE), Hydrosonography (DEVICE).
Who is sponsoring clinical trial NCT06394752?
This trial is sponsored by Center for Reproductive Health & Gynecology, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06394752 being conducted?
This trial has 2 study locations across California, Nayarit. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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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 NCT06394752's enrollment target sits among peer trials
100 9th of 18 higher than 10 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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