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RECRUITING 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.

NCT06394752 · View on ClinicalTrials.gov ↗

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

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06394752

The ClinicalTrials.gov registry entry for NCT06394752 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Center for Reproductive Health & Gynecology, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 7 conditions, with Fertility Issues appearing as the primary indexed condition, and to 2 interventions — of which Visual Saline Infusion is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06394752 reports 2 study locations spanning 2 distinct geographic areas — top geographies include California, Nayarit. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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: Fertility Issues, Gynecology, Infertility Female, Hysteroscopy, Hysteroscopy Technique. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06394752?

The interventions under investigation include: Visual Saline Infusion (DEVICE), Hydrosonography (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

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. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

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