NCT02891174View on ClinicalTrials.gov

The Effect of Ibuprofen on Post-partum Blood Pressure in Women With Hypertensive Disorders of Pregnancy

PHASE4CompletedINTERVENTIONAL
Enrollment

74

Participants

Timeline

Start Date

December 1, 2016

Primary Completion Date

March 31, 2018

Study Completion Date

June 20, 2018

Conditions
Hypertension, Pregnancy-InducedPre-eclampsia
Interventions
DRUG

Ibuprofen

At the time of delivery, eligibility will be reviewed. If the participant remains eligible, she will be randomized by the study pharmacy to begin post-partum analgesic therapy with ibuprofen followed by acetaminophen.

DRUG

Acetaminophen

At the time of delivery, eligibility will be reviewed. If the participant remains eligible, she will be randomized by the study pharmacy to begin post-partum analgesic therapy with acetaminophen followed by ibuprofen.

Trial Locations (1)

48109

University of Michigan, Ann Arbor

All Listed Sponsors
lead

University of Michigan

OTHER

NCT02891174 - The Effect of Ibuprofen on Post-partum Blood Pressure in Women With Hypertensive Disorders of Pregnancy | Biotech Hunter | Biotech Hunter