Aviso: Este site agrega dados públicos oficiais da FDA, ClinicalTrials.gov, PubMed e SEC EDGAR apenas para referência geral. Não constitui aconselhamento médico, diagnóstico, recomendação de tratamento ou aconselhamento de investimento.

Ensaio clínico

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

NCT: NCT07387380 · COMPLETED

ID NCTNCT07387380
EstadoCOMPLETED
Data de início2026-01-06
Conclusão2026-04-05
SponsorLucie Medical Inc (INDUSTRY)
First posted
Last updated

Resumo breve

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.

Fonte oficial

Ver no ClinicalTrials.gov →

Dados provenientes da API do ClinicalTrials.gov. Para consultar o estado mais recente, veja o registo oficial.

↑