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 @ 8:00 PM
Ignite Modification Date:
2025-12-24 @ 8:00 PM
NCT ID:
NCT00370604
Eligibility Criteria:
Inclusion Criteria:
* American Society of Anesthesiologists status 1 to 2
* Must have provided written informed consent = or \< 6cm cervical dilation
* Fetus 37 to 42 weeks gestation
* Must be able to read and write English well enough to provide written informed consent
Exclusion Criteria:
* BMI = or \> 40
* Multiple gestation pregnancy
* Known contraindications to use of epidural analgesia
* Pregnancy-induced hypertension
* Investigator concern for maternal or neonatal welfare
* Receipt of spinal or epidural anesthesia within 14 days of labour epidural request
* Women with chronic headaches (defined as headaches that occur 15 or more days per month for more than 3 months)
* Already participated in study
* History of narcotic abuse
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT00370604
Study Brief:
Protocol Section:
NCT00370604