Hypertension in Pregnancy Clinical Trial
— ACEOfficial title:
Oral Combined Hydrochlorothiazide/Lisinopril Versus Oral Nifedipine for Postpartum Hypertension: A Comparative Effectiveness Pilot Randomized Controlled Trial
Verified date | July 2023 |
Source | The University of Texas Health Science Center, Houston |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to see if a combined pill of Angiotensin-converting enzyme (ACE) inhibitors (a medication that helps relax your veins and arteries to lower your blood pressure) with diuretics (sometimes called water pills, help rid your body of salt and water) will control blood pressure better than a different blood pressure medication of calcium channel blocker (lower your blood pressure by preventing calcium from entering the cells of your heart and arteries). Both medications are part of our usual care for high blood pressure after delivery.
Status | Active, not recruiting |
Enrollment | 70 |
Est. completion date | October 1, 2023 |
Est. primary completion date | June 26, 2022 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Postpartum women at = 18 years of age - Postpartum diagnosis of persistent hypertension (2 measurements of Systolic BP =150 and/or diastolic BP = 100 or systolic BP =140 and/or diastolic BP = 90 for people with diabetes) requiring an oral medication based on the ACOG criteria or - Hypertensive disorder of pregnancy diagnosed antepartum or intrapartum requiring blood pressure medication in the postpartum - Chronic hypertension requiring blood pressure medication postpartum Exclusion Criteria: - Urine output < 30 cc/h prior to screening for eligibility - Creatinine > 1.4 during current admission - End-stage renal disease - Hypersensitivity to ACE inhibitors or sulfa drugs - Idiopathic/hereditary angioedema - Hyperkalemia (serum potassium >5 mEq/L) during current admission - Pulmonary edema |
Country | Name | City | State |
---|---|---|---|
United States | University of Texas Health Science Center | Houston | Texas |
Lead Sponsor | Collaborator |
---|---|
The University of Texas Health Science Center, Houston |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of Participants With Stage 2 Hypertension | Stage 2 hypertension at day 7-10 after delivery (defined as SBP = 140 and/or DBP = 90 mmHg) or admission to the hospital for blood pressure control prior to day 10.
Primary outcome will be calculated as the average BP reading for day 7-10 after delivery. |
7-10 after delivery | |
Secondary | Number of Participants With Severe Postpartum Hypertension | severe postpartum hypertension (SBP=160 and/or DBP=110 mmHg on 2 occasions, 15 minutes apart) | 7-10 after delivery | |
Secondary | Number of Participants Who Received Additional Antihypertensive During Admission | number of participants who received additional antihypertensive during admission, at 7-10 days postpartum. | 7-10 days postpartum | |
Secondary | Postpartum Length of Stay | time spent in hospital following delivery | up to 30 days after delivery | |
Secondary | Postpartum Readmission | occurrence of returning to hospital for admission postpartum | up to 30 days after delivery | |
Secondary | Time to Blood Pressure Control | The time from delivery to Blood Pressure control (i.e time from delivery to last BP <150/100). | 10 days | |
Secondary | Incidence of Persistent Postpartum Hypertension | Incidence of persistent postpartum hypertension 6 weeks postpartum (SBP = 140 and/or DBP = 90 mmHg). | 6 weeks postpartum | |
Secondary | Occurrence of Proteinuria | Proteinuria is measured by urine protein creatinine ratio | 7-10 days, and 6 weeks postpartum | |
Secondary | Presense of Labs Abnormality | Labs abnormality including hyperkalemia or creatinine increase | 7-10 days, and 6 weeks postpartum | |
Secondary | Compliance With Medications | Compliance with medications. The patient will be asked to bring their medication bottle with them and the compliance will be measured by counting pills at each postpartum visit. | at the time of the 1st postpartum clinic visit, which is about 6 to 37 days after birth | |
Secondary | Time to Control Blood Pressure | Blood pressure at 3 month, 6 month, 9 month, 1 year after delivery and need for BP medications. Definition of controlled blood pressure is (SBP < 140 and/or DBP < 90 mmHg). This will be assessed by telephone encounter with the patient | 3 month-1 year | |
Secondary | Percentage of Patients Receiving Primary Care With BP Measurement | Percentage of patients receiving primary care with BP measurement at 1 year | 1 year postpartum | |
Secondary | Postpartum Complications- Number of Participants With ICU Admission | Need for ICU admission | 10 days postpartum | |
Secondary | Postpartum Complications- Number of Participants With HELLP (Hemolysis, Elevated Liver Enzymes and Low Platelets) Syndrome | Hemolysis, elevated liver enzymes, low platelet count: HELLP | 10 days postpartum | |
Secondary | Postpartum Complications- Number of Participants With Eclampsia | Eclampsia, which is considered a complication of severe preeclampsia, is commonly defined as new onset of grand mal seizure activity and/or unexplained coma during pregnancy or postpartum in a woman with signs or symptoms of preeclampsia. | 10 days postpartum | |
Secondary | Postpartum Complications- Number of Participants With Stroke | Stroke | 10 days postpartum | |
Secondary | Postpartum Complications- Number of Participants With Renal Failure | Renal failure | 10 days postpartum | |
Secondary | Postpartum Complications- Number of Participants With Pulmonary Edema | Pulmonary edema | 10 days postpartum | |
Secondary | Postpartum Complications - Number of Participants With Cardiomyopathy | Cardiomyopathy | 10 days postpartum | |
Secondary | Postpartum Complications- Number of Participants With Maternal Death | Maternal death | 10 days postpartum | |
Secondary | Receipt of Additional Antihypertensive During Admission | Receipt of additional antihypertensive during admission at 6 weeks postpartum | 6 weeks postpartum |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT00974714 -
L-arginine Effects on Chronic Hypertension in Pregnancy
|
Phase 3 | |
Terminated |
NCT03595982 -
Is Procardia XL 60 mg Q Daily Equivalent to 30 mg XL Given Twice Daily?
|
Phase 4 | |
Completed |
NCT04486170 -
Assessment of Postpartum Education to Improve Compliance
|
N/A | |
Completed |
NCT03506724 -
Response to Anti-hypertensives in Pregnant and Postpartum Patients
|
Phase 4 | |
Completed |
NCT03613714 -
Innovation in Postpartum Care for Women With Hypertensive Disorders of Pregnancy
|
N/A | |
Recruiting |
NCT04604535 -
The BEET-BP Trial - Investigating the Effect of Dietary Nitrates on Hypertension in Pregnancy
|
N/A | |
Completed |
NCT00412230 -
Insulin Resistance and Hypertensive Disorders in Pregnancy
|
N/A | |
Completed |
NCT04119232 -
Randomized Clinical Trial to Increase Physical Activity After a a Hypertensive Pregnancy
|
N/A | |
Completed |
NCT04633551 -
Vascular Inflammation and Anti-inflammatory Supplements After Adverse Pregnancy Outcomes
|
N/A | |
Completed |
NCT05859282 -
Development and Validation of a Short Tool to Assess the Awareness of Pregnancy-induced Hypertension
|
||
Active, not recruiting |
NCT05543265 -
Bridging the Gap From Postpartum to Primary Care
|
N/A | |
Completed |
NCT00571766 -
Effects of Oral L-Arginine on Chronic Hypertension in Pregnancy
|
Phase 3 | |
Recruiting |
NCT05473767 -
Expanding the Family Check-Up in Early Childhood to Promote Cardiovascular Health of Mothers and Young Children
|
N/A | |
Recruiting |
NCT05683093 -
Cardiovascular Longitudinal ALSPAC Research Investigations Following Hypertensive Pregnancy in Young Adulthood
|
||
Completed |
NCT06403722 -
Perinatal Outcomes in Patients With Elevated sFlt-1/PlGF Ratio
|
||
Recruiting |
NCT05852054 -
Supporting Transitions to Primary Care Among Under-resourced, Postpartum Women (STEP-UP)
|
Phase 3 | |
Recruiting |
NCT05137808 -
Understanding Blood Pressure Changes After Birth
|
||
Completed |
NCT03961360 -
Effectiveness of Higher Aspirin Dosing for Prevention of Preeclampsia in High Risk Obese Gravida
|
Phase 2/Phase 3 | |
Active, not recruiting |
NCT03648645 -
Hypertensive Pregnant Women Monitored by Teletransmitted Self-measurements of Blood Pressure
|
N/A | |
Recruiting |
NCT06054841 -
Reshaping Postpartum Follow-up
|
N/A |