Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Gestational Hypertension
  • Hypertension Pregnancy-induced
  • Postpartum Preeclampsia
  • Postpartum Pregnancy-Induced Hypertension
  • Pre Eclampsia
  • Superimposed Pre-Eclampsia
Type
Interventional
Phase
Phase 3
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: double-blind randomized placebo controlled clinical trialMasking: Triple (Participant, Care Provider, Investigator)Masking Description: Randomization will be performed by a person not involved in the clinical trial using a computer random list of numbers generated using STATA (StataCorp 14.0, Dallas, TX). This list of random number assignments will be kept secure and sent directly to the investigational drug service (IDS), who will be responsible for the allocation and dispensing of the medicationsPrimary Purpose: Prevention

Participation Requirements

Age
Between 18 years and 50 years
Gender
Only males

Description

To evaluate effectiveness of hydrochlorothiazide prophylaxis on prophylaxis, prevention and relapse of preeclampsia or gestational hypertension on readmission rates, need for additional antihypertensive therapy and number of triage visits.

To evaluate effectiveness of hydrochlorothiazide prophylaxis on prophylaxis, prevention and relapse of preeclampsia or gestational hypertension on readmission rates, need for additional antihypertensive therapy and number of triage visits.

Tracking Information

NCT #
NCT03298802
Collaborators
Not Provided
Investigators
Principal Investigator: Antonio Saad, M.D. UTMB