Hypertension, Pregnancy Induced Clinical Trial
Official title:
Hydralazine vs. Labetalol for the Management of Hypertensive Crisis in Patients With Hypertensive Disorders of Pregnancy. A Randomized Controlled Trial.
Verified date | May 2013 |
Source | Saint Thomas Hospital, Panama |
Contact | n/a |
Is FDA regulated | No |
Health authority | Panama: Ministry of Health |
Study type | Interventional |
Hypertensive crisis (defined as a systolic pressure > 160mmHg or a diastolic pressure > 110mmHg) in patients with a hypertensive disorder of pregnancy is a serious complication with severe and even deadly consequences. The management in this population had been studied, but no consensus has been reached with regards to which treatment is better. Our study will compare two drugs: Hydralazine and Labetalol for the management of hypertensive crisis.
Status | Completed |
Enrollment | 261 |
Est. completion date | May 2013 |
Est. primary completion date | April 2013 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Gestational age > 24 weeks. - Hypertensive Crisis (systolic pressure > 160 mmHg / diastolic pressure < 110mmHg). Exclusion Criteria: - Known allergy to hydralazine. - Known allergy to labetalol. - Severe Bradycardia |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Panama | Saint Thomas Maternity Hospital | Panama |
Lead Sponsor | Collaborator |
---|---|
Saint Thomas Hospital, Panama |
Panama,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Control of Hypertensive Crisis | Number of patients with hypertensive crisis in which the blood pressure is controlled with the use of the assigned drug, without requiring additional medications. | 10 months | No |
Secondary | Adverse reactions | Number of patients in each group that reported an adverse reaction to the drug assigned. | 10 months | Yes |
Secondary | Number of doses | Number of doses of the assigned drug required to lower blood pressure, without requiring additional medication. | 10 months | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01911494 -
Community Level Interventions for Pre-eclampsia
|
N/A | |
Recruiting |
NCT06100484 -
Blood Pressure Variability Effect on Right Ventricular Strain in Women With Hypertensive Disorders With Pregnancy
|
||
Completed |
NCT02050529 -
Randomized Controlled Trial of Labetalol Versus Hydralazine for Severe Hypertension in Obstetric Patients.
|
Phase 2 | |
Recruiting |
NCT06069102 -
Optimal Blood Pressure Treatment Thresholds Postpartum
|
Phase 4 | |
Recruiting |
NCT06281665 -
Treatment With Aspirin After Preeclampsia: TAP Trial
|
Phase 4 | |
Not yet recruiting |
NCT05826925 -
Optimizing Cardiovascular Preventive Care for Women Following Hypertensive Disorders of Pregnancy
|
N/A | |
Not yet recruiting |
NCT05460416 -
Treatment Preventive for Pre-eclampsia by Acetylsalicylic Acid in Women Who Underwent Frozen Embryo Transfer
|
Phase 4 |