Clinical Trial

KIRA Uterine Drain Device Evaluation- First-In- Human Study

Study acronym: RANI
Completed
View on ClinicalTrials.gov →
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.
Protocol Amendment History 3 changes
critical Trial completed 2026-05-19
notable Primary completion moved earlier: 2026-06 -> 2026-04-05 2026-05-19
minor Completion moved earlier: 2026-06 -> 2026-04-05 2026-05-19
Trial Details
NCT Number NCT07387380
Lead Sponsor Lucie Medical Inc
Conditions Cesarean Delivery Procedures
Enrollment 10 participants
Start Date 2026-01-06
Primary Completion 2026-04-05 (estimated)
Study Completion 2026-04-05 (estimated)
Updated on ClinicalTrials.gov 2026-05-18