Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 5:29 PM
Ignite Modification Date:
2025-12-24 @ 5:29 PM
NCT ID:
NCT01599468
Eligibility Criteria:
Inclusion Criteria:
* ASA1 parturients
* aged from 20 to 40
* correct preoperative haemostatic status (prothrombine ratio \> 60 % and platelet rate \> 100 000),
* cesarean section under spinal anesthesia complicated by uterine atony needing the introduction of Sulprostone
Exclusion Criteria:
* abnormal placentation
* severe pre-eclampsia
* coagulopathy and uterine rupture
* the contra indications of TXA : past history of vascular occlusive event, convulsion, and allergy.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
40 Years
Study:
NCT01599468
Study Brief:
Protocol Section:
NCT01599468