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COMPLETED NA

Pannus Assistance Needed for Obstetric Ultrasound Studies

NCT05764408 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this randomized controlled trial is to evaluate whether use of a pannus retractor adhesive improves fetal anatomic ultrasound examinations. The primary question it aims to answer is: • Does the use of a pannus retractor adhesive increase the rate of detailed anatomic survey completion, defined by satisfactory visualization of sixteen prespecified fetal anatomy views, for participants with a pannus and body mass index of at least 40 kg/m2?

Interventions

  • DEVICE traxi® Panniculus Retractor

Study Locations (1)

South Carolina

  • Prisma Health — Greenville

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2023-03-10
Est. Completion 2023-07-13
Phase NA

Sponsor

Prisma Health-Upstate

19 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05764408

The ClinicalTrials.gov registry entry for NCT05764408 describes a study currently listed as completed. 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 150 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Prisma Health-Upstate, which has 19 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Fetal Anomaly appearing as the primary indexed condition, and to 1 intervention — of which traxi® Panniculus Retractor 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: NCT05764408 reports 1 study location spanning 1 distinct geographic area — top geographies include South Carolina. 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 NCT05764408 about?

NCT05764408 is a clinical study titled "Pannus Assistance Needed for Obstetric Ultrasound Studies". The goal of this randomized controlled trial is to evaluate whether use of a pannus retractor adhesive improves fetal anatomic ultrasound examinations. The primary question it aims to answer is: • Does the use of a pannus retractor adhesive increase the rate of detailed anatomic survey completion, ...

What is the current status of trial NCT05764408?

This trial is currently completed. It is a NA study. The enrollment target is 150 participants. The study started on 2023-03-10. Estimated completion is 2023-07-13.

What conditions does trial NCT05764408 study?

This clinical trial studies the following conditions: Fetal Anomaly, Obesity Complicating Childbirth. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05764408?

The interventions under investigation include: traxi® Panniculus Retractor (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05764408?

This trial is sponsored by Prisma Health-Upstate, which has 19 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05764408 being conducted?

This trial has 1 study location across South Carolina. 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