Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT04362592 · ClinicalTrials.gov registry record · NA
In-Utero Endoscopic Correction of Spina Bifida
A NA study of Spina Bifida and Myelomeningocele, sponsored by University of Southern California.
- Recruiting
- Registry status
- NA
- Development phase
- 110
- Enrollment target
- 2
- Study locations
NCT04362592 is a NA study of Spina Bifida and Myelomeningocele that is actively recruiting participants, run by University of Southern California. The registered enrollment target is 110 participants, above the 46-participant average among 16 other Spina Bifida trials with a reported enrollment target (139% higher). The trial reports 2 study locations across 2 states.
The verdict
NCT04362592, a NA study of Spina Bifida and Myelomeningocele, is actively recruiting participants, sponsored by University of Southern California.
- RECRUITING
- Registry status
- NA
- Development phase
- 110 participants
- Enrollment target
- 2
- Study locations
Study Summary
The purpose of this study is to evaluate the feasibility and effectiveness of performing fetoscopic surgical correction of fetal spina bifida. Two surgical approaches will be utilized: the percutaneous technique versus the laparotomy/uterine exteriorization technique.
Conditions Studied
Interventions
- DEVICE In Utero Endoscopic Correction of Myelomeningocele IDE - Percutaneous Technique
- DEVICE In Utero Endoscopic Correction of Myelomeningocele IDE - Laparotomy/Uterine Exteriorization Technique
Study Locations (2)
California
- Hollywood Presbyterian Medical Center - Los Angeles
Florida
- Wellington Regional Medical Center - Wellington
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 110 participants |
| Start Date | 2018-11-02 |
| Est. Completion | 2031-10-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04362592
The ClinicalTrials.gov registry entry for NCT04362592 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 110 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 46-participant average among 16 other Spina Bifida trials with a reported enrollment target (139% higher). The listed sponsor is University of Southern California, which has 617 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Spina Bifida appearing as the primary indexed condition, and to 2 interventions - of which In Utero Endoscopic Correction of Myelomeningocele IDE - Percutaneous Technique is the first listed.
NCT04362592 reports 2 study locations spanning 2 distinct geographic areas - top geographies include California, Florida.
Frequently Asked Questions
What is clinical trial NCT04362592 about?
NCT04362592 is a clinical study titled "In-Utero Endoscopic Correction of Spina Bifida". The purpose of this study is to evaluate the feasibility and effectiveness of performing fetoscopic surgical correction of fetal spina bifida. Two surgical approaches will be utilized: the percutaneous technique versus the laparotomy/uterine exteriorization technique.
What is the current status of trial NCT04362592?
This trial is currently recruiting. It is a NA study. The enrollment target is 110 participants. The study started on 2018-11-02. Estimated completion is 2031-10-31.
What conditions does trial NCT04362592 study?
This clinical trial studies the following conditions: Spina Bifida, Myelomeningocele, Neural Tube Defects.
What interventions are being tested in trial NCT04362592?
The interventions under investigation include: In Utero Endoscopic Correction of Myelomeningocele IDE - Percutaneous Technique (DEVICE), In Utero Endoscopic Correction of Myelomeningocele IDE - Laparotomy/Uterine Exteriorization Technique (DEVICE).
Who is sponsoring clinical trial NCT04362592?
This trial is sponsored by University of Southern California, which has 617 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04362592 being conducted?
This trial has 2 study locations across California, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Spina Bifida
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.
-
Evaluating Long-term Use of a Pediatric Robotic Exoskeleton (P.REX/Agilik) to Improve Gait in Children With Movement Disorders
RECRUITING · NA
-
Transcutaneous Tibial Nerve Stimulation (TTNS) Treatment in Spina Bifida Pediatric Patients With Neurogenic Bladder
RECRUITING · NA
-
Laparotomy Versus Percutaneous Endoscopic Correction of Myelomeningocele
RECRUITING · NA
-
Autologous Human Umbilical Cord Tissue Patch for Postnatal Closure of Open Neural Tube Defects
RECRUITING · NA
-
Transcutaneous Spinal Stimulation for Children and Youth With Spina Bifida
RECRUITING · NA
-
Mobile Health Self-Management and Support System for Chronic and Complex Health Conditions
RECRUITING · NA
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.