CompletedNot Applicable

Tranexamic Acid for Postpartum Vaginal Laceration Hemorrhage

Turkey (Türkiye)161 participantsStarted 2024-01-01

Plain-language summary

The necessary information was provided to the patients included in the study and their written consent was obtained.

Who can participate

Age range20 Years – 35 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Study Population: 161 women aged 20-35 years who had spontaneous vaginal deliveries. Sampling Method: Non-Probability Sample Minimum Age: 20 Years Maximum Age: 35 Years Sex: Female Gender Based: Yes Accepts Healthy Volunteers: Yes Criteria: Inclusion Criteria: Vaginal delivery without episiotomy Presence of superficial vaginal lacerations Postpartum blood loss not exceeding 500 ml Age between 20 and 35 years Informed consent obtained Exclusion Criteria: Cesarean delivery Episiotomy or vaginal lacerations requiring suturing Postpartum bleeding exceeding 500 ml Pre-existing coagulation disorders Tranexamic acid allergy \-

What they're measuring

Total Postpartum Blood Loss

Timeframe: Within the first 3 hours after delivery

Trial details

NCT IDNCT07094399

SponsorHarran University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2024-11-30

View on ClinicalTrials.gov More Postpartum Hemorrhage trials