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NCT07387380 · ClinicalTrials.gov registry record · NA
KIRA Uterine Drain Device Evaluation- First-In- Human Study
A NA study of Cesarean Delivery Procedures, sponsored by Lucie Medical.
- Recruiting
- Registry status
- NA
- Development phase
- 10
- Enrollment target
- 1
- Study location
NCT07387380 is a NA study of Cesarean Delivery Procedures that is actively recruiting participants, run by Lucie Medical. The registered enrollment target is 10 participants. The trial reports 1 study location across 1 state.
The verdict
NCT07387380, a NA study of Cesarean Delivery Procedures, is actively recruiting participants, sponsored by Lucie Medical.
- RECRUITING
- Registry status
- NA
- Development phase
- 10 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this research is to evaluate a new investigational medical device, the Kira device, intended to make it easier for the surgical team to monitor blood loss during and immediately after cesarean deliveries (c-sections). This study will assess the safety of the device and the device's ability to gently suction blood from the uterus into a clear container where it can be seen and measured by the surgical team.
Conditions Studied
Interventions
- DEVICE Uterine drain for use in cesarean section
Study Locations (1)
Ohio
- Ohio State University - Columbus
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2026-01-06 |
| Est. Completion | 2026-06 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07387380
The ClinicalTrials.gov registry entry for NCT07387380 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Lucie Medical, which has 1 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Cesarean Delivery Procedures appearing as the primary indexed condition, and to 1 intervention - of which Uterine drain for use in cesarean section is the first listed.
NCT07387380 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.
Frequently Asked Questions
What is clinical trial NCT07387380 about?
NCT07387380 is a clinical study titled "KIRA Uterine Drain Device Evaluation- First-In- Human Study". The purpose of this research is to evaluate a new investigational medical device, the Kira device, intended to make it easier for the surgical team to monitor blood loss during and immediately after cesarean deliveries (c-sections). This study will assess the safety of the device and the device's ab...
What is the current status of trial NCT07387380?
This trial is currently recruiting. It is a NA study. The enrollment target is 10 participants. The study started on 2026-01-06. Estimated completion is 2026-06.
What conditions does trial NCT07387380 study?
This clinical trial studies the following conditions: Cesarean Delivery Procedures.
What interventions are being tested in trial NCT07387380?
The interventions under investigation include: Uterine drain for use in cesarean section (DEVICE).
Who is sponsoring clinical trial NCT07387380?
This trial is sponsored by Lucie Medical, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07387380 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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