Enhanced Recovery at Cesarean Birth to Improve Postoperative Outcomes and Reduce Postoperative Length of Stay

Completed · Phase 2

Conditions studied: Cesarean Section

In brief

To determine whether women randomized to an enhanced recovery program will have improved postoperative outcomes including improved breastfeeding initiation and continuation, reduction in hospital length of stay without compromising patient satisfaction in comparison to standard postoperative recovery interventions.

Key facts

Study ID

NCT02956616

Run by

Montefiore Medical Center

People needed

118

Starts

2017-09-01

Expected to finish

2018-06-15

Last updated by the study team

2019-04-25

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Women undergoing a non-urgent or elective cesarean delivery >37 weeks gestation

You may not qualify if…

• Women undergoing an urgent or emergent cesarean birth
• Women less than 18 years old
• Patients receiving general anesthesia
• Abnormally adherent placenta (Placenta Accreta) or expected excessive blood loss (Placenta accreta)
• Pre-existing essential hypertension or hypertensive disorders of pregnancy (preeclampsia, eclampsia, HELLP)
• Chronic or acute renal impairment
• Bleeding disorders or platelet dysfunction
• Peptic ulcer disease or gastrointestinal bleeding
• Known hypersensitivity to ketorolac (toradol)
• Active infection at the time of cesarean
• Cesarean birth prior to 37 weeks
• Women in significant pain in labor

Where it is running

• Montefiore Medical Center — The Bronx, New York, United States

Full record on ClinicalTrials.gov

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