Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT06284421 · ClinicalTrials.gov registry record · NA
Durometer for Measuring Uterine Tone
A NA study of Cesarean Section Complications and Uterine Tone Disorders, sponsored by University of Chicago.
- Recruiting
- Registry status
- NA
- Development phase
- 20
- Enrollment target
- 1
- Study location
NCT06284421: Recruiting NA study of Cesarean Section Complications and Uterine Tone Disorders, sponsored by University of Chicago.
NCT06284421 is a NA study of Cesarean Section Complications and Uterine Tone Disorders that is actively recruiting participants, run by University of Chicago. The registered enrollment target is 20 participants, below the 771-participant average among 9 other Cesarean Section Complications trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06284421, a NA study of Cesarean Section Complications and Uterine Tone Disorders, is actively recruiting participants, sponsored by University of Chicago.
- RECRUITING
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
This study will evaluate the use of a durometer to measure uterine tone in parturients undergoing cesarean delivery.
Primary Outcome
The primary outcome will be the ability to obtain reliable readings of the 'hardness' of the uterus during a cesarean delivery.
Conditions Studied
Interventions
- DEVICE Shore durometer
Study Locations (1)
Illinois
- University of Chicago - Chicago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2024-02-08 |
| Est. Completion | 2026-08-30 |
| Phase | NA |
What NCT06284421 shows while recruiting
NCT06284421 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 771-participant average among 9 other Cesarean Section Complications trials with a reported enrollment target (97% lower).
The record links to 2 conditions, with Cesarean Section Complications appearing as the primary indexed condition, and to 1 intervention - of which Shore durometer is the first listed.
NCT06284421 reports a single indexed study location in Illinois.
Frequently Asked Questions
What is clinical trial NCT06284421 about?
NCT06284421 is a clinical study titled "Durometer for Measuring Uterine Tone". This study will evaluate the use of a durometer to measure uterine tone in parturients undergoing cesarean delivery.
What is the current status of trial NCT06284421?
This trial is currently recruiting. It is a NA study. The enrollment target is 20 participants. The study started on 2024-02-08. Estimated completion is 2026-08-30.
What conditions does trial NCT06284421 study?
This clinical trial studies the following conditions: Cesarean Section Complications, Uterine Tone Disorders.
What interventions are being tested in trial NCT06284421?
The interventions under investigation include: Shore durometer (DEVICE).
Who is sponsoring clinical trial NCT06284421?
This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06284421 being conducted?
This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Cesarean Section Complications
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.
Where NCT06284421's enrollment target sits among peer trials
20 10th of 9 the lowest of 9 other Cesarean Section Complications trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Cesarean Section Complications trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
-
Wound Irrigation With Saline Versus Hypodilute-chlorhexidine After Cesarean Section (WISHES Study)
RECRUITING · NA
-
Personalized Perioperative Analgesia Platform (PPAP) for Cesarean Section
RECRUITING · NA
-
An Evaluation of the Team Birth Project
COMPLETED · NA
-
Oxytocin Pharmacokinetics and Pharmacodynamics
RECRUITING · Phase 2
-
Calcium Chloride for Prevention of Blood Loss During Intrapartum Cesarean Delivery
COMPLETED · Phase 3
-
Arm and Ankle Blood Pressure Cuffs During C-Section
COMPLETED
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT00573339 · 20 participants
Cardiac Magnetic Resonance Imaging (MRI) Normal Reference Control Group Testing
- NCT00692939 · 20 participants · Phase 1
Autologous Stem Cell Transplantation for Crohn's Disease
- NCT00967785 · 20 participants · Phase 1
A Phase I Study of Mozobil in the Treatment of Patients With WHIMS
- NCT01406691 · 20 participants · Phase 4
Light Flashes to Treat Delayed Sleep Phase Disorder (DSPD)
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI