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 @ 3:06 PM
Ignite Modification Date:
2025-12-24 @ 3:06 PM
NCT ID:
NCT01741259
Eligibility Criteria:
Inclusion Criteria are as follows:
* Over the age of 18
* Undergoing non-urgent, non-emergent cesarean section at Mercy Hospital St. Louis
Exclusion Criteria:
* non-English speaking
* mentally disabled
* allergy to meperidine
* seizure disorder
* renal impairment defined as a serum creatinine \>0.8 mg/dL or patients who give a history of renal impairment
* fever greater than 101
* patients receiving low molecular weight heparin at any dose or unfractionated heparin at doses greater than 5000 u subcutaneous twice daily
* pre-eclampsia requiring magnesium due to post-partum room assignment
* obstructive sleep apnea due to post-partum room assignment
* post-partum hemorrhage due to post-partum room assignment
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
50 Years
Study:
NCT01741259
Study Brief:
Protocol Section:
NCT01741259