MedTrace Logo

Hypertension In Postpartum Preeclampsia Study

NCT03011567 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 202

Last updated 2024-01-03

Study results available
· View outcomes & findings →

Summary

This study aims to evaluate whether NSAIDs (Non-steroidal antiinflammatory drugs) administered during the postpartum period influence blood pressure in women with hypertensive disorders of pregnancy. The study design is a prospective double blinded randomized control trial with participants randomized to receive postpartum analgesic regimens with and without NSAIDs.

Conditions

  • Hypertension, Pregnancy-Induced

Interventions

DRUG

Acetaminophen

Participants will receive acetaminophen for postpartum mild pain relief

DRUG

Ibuprofen

Participants will receive ibuprofen for postpartum mild pain relief

Sponsors & Collaborators

  • MemorialCare Health System

    lead OTHER

Principal Investigators

  • Jennifer McNulty, MD · Long Beach Memorial Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-01-31
Primary Completion
2019-10-31
Completion
2019-10-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03011567 on ClinicalTrials.gov