Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT06488092 · ClinicalTrials.gov registry record · NA
IC-CS Risk: Patient Outcomes
A NA study of Cesarean Delivery, sponsored by University of Pennsylvania.
- Active
- Registry status
- NA
- Development phase
- 20,000
- Enrollment target
- 14
- Study locations
NCT06488092 is a NA study of Cesarean Delivery that is active but no longer recruiting, run by University of Pennsylvania. The registered enrollment target is 20,000 participants, above the 1,483-participant average among 10 other Cesarean Delivery trials with a reported enrollment target (1249% higher). The trial reports 14 study locations across 5 states.
The verdict
NCT06488092, a NA study of Cesarean Delivery, is active but no longer recruiting, sponsored by University of Pennsylvania.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 20,000 participants
- Enrollment target
- 14
- Study locations
Study Summary
This study is looking at the impact of the implementation of a cesarean risk calculator on cesarean delivery and maternal morbidity rates.
Conditions Studied
Interventions
- OTHER Cesarean Risk Calculator
Study Locations (14)
Michigan
- University of Michigan - Ann Arbor
- Henry Ford Macomb Hospital - Clinton Township
- Henry Ford Hospital - Detroit
- E.W. Sparrow Hospital - Lansing
Utah
- Logan Regional Hospital-Intermountain Healthcare - Logan
- McKay-Dee Hospital - Ogden
- Riverton Hospital-Intermountain Healthcare - Riverton
- University of Utah Hospital - Salt Lake City
Ohio
- Akron General - Akron
- Fairview Hospital - Cleveland
- Hillcrest Hospital - Mayfield Heights
Pennsylvania
- Lancaster General Health - Lancaster
- Chester County Hosptial - West Chester
New Jersey
- Princeton Medical Center - Plainsboro
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20,000 participants |
| Start Date | 2024-09-01 |
| Est. Completion | 2027-09 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06488092
The ClinicalTrials.gov registry entry for NCT06488092 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 20,000 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 1,483-participant average among 10 other Cesarean Delivery trials with a reported enrollment target (1249% higher). The listed sponsor is University of Pennsylvania, which has 1,423 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Cesarean Delivery appearing as the primary indexed condition, and to 1 intervention - of which Cesarean Risk Calculator is the first listed.
NCT06488092 reports 14 study locations spanning 5 distinct geographic areas - top geographies include Michigan, Utah, Ohio.
Frequently Asked Questions
What is clinical trial NCT06488092 about?
NCT06488092 is a clinical study titled "IC-CS Risk: Patient Outcomes". This study is looking at the impact of the implementation of a cesarean risk calculator on cesarean delivery and maternal morbidity rates.
What is the current status of trial NCT06488092?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 20,000 participants. The study started on 2024-09-01. Estimated completion is 2027-09.
What conditions does trial NCT06488092 study?
This clinical trial studies the following conditions: Cesarean Delivery.
What interventions are being tested in trial NCT06488092?
The interventions under investigation include: Cesarean Risk Calculator (OTHER).
Who is sponsoring clinical trial NCT06488092?
This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06488092 being conducted?
This trial has 14 study locations across Michigan, New Jersey, Ohio, Pennsylvania, Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Cesarean Delivery
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.
-
Post-Operative Cesarean Section Cosmesis
RECRUITING · NA
-
Induction of Labor After Cesarean Using Foley Alone vs. Concurrent Foley and Oxytocin
RECRUITING · NA
-
Delayed Cord Clamping at Term Cesarean
COMPLETED · NA
-
COMFORT Trial: Complex Obstetric Management With Focused Regional Transversus Abdominis Plane Block
RECRUITING · Phase 4
-
The Society for Obstetric Anesthesia and Perinatology Research Network General Anesthesia Registry
RECRUITING
-
Post-cesarean Analgesia: Comparing Effectiveness of Staggered v. Simultaneous Therapies
RECRUITING · Phase 4
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.