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:
2025-12-25 @ 12:34 AM
Ignite Modification Date:
2025-12-25 @ 12:34 AM
NCT ID:
NCT03478267
Eligibility Criteria:
Inclusion Criteria:
* Pregnant women between 32 and 41 weeks' gestation undergoing either vaginal or cesarean delivery with a fetal baseline heart rate of 110-130 beats per minute and 140-160 beats per minute.
Exclusion Criteria:
1. Delivery before 32 weeks of gestation
2. Maternal bradycardic (\<60) or tachycardic (\>100) resting heart rate.
3. Fetal bradycardia (\<110) or tachycardia (\>160).
4. Suspected chorioamnionitis
5. Maternal diseases which can affect her heart rate such as:
1. Cardiac disease (including arrhythmias)
2. Diseases of the thyroid gland
3. Rheumatic diseases
6. Use of medication which alters heart rate such as:
1. Beta blockers
2. Beta agonists
3. Cocaine, amphetamines
7. Use of Pethidine and Phenergan during delivery
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
44 Years
Study:
NCT03478267
Study Brief:
Protocol Section:
NCT03478267