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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 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.

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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.

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

FieldValue
Enrollment Target 100 participants
Start Date 2024-04-25
Est. Completion 2025-07-30
Phase NA

What the Registry Record Tells You About NCT06394752

The ClinicalTrials.gov registry entry for NCT06394752 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 377-participant average among 18 other Infertility, Female trials with a reported enrollment target (73% lower). The listed sponsor is Center for Reproductive Health & Gynecology, which has 1 total studies on file at ClinicalTrials.gov.

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 2 study locations spanning 2 distinct geographic areas - top geographies include 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.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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