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Clonidine Versus Captopril for Treatment of Postpartum Very High Blood Pressure (CLONCAP)

Primary Purpose

Preeclampsia

Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
CLONIDINE
CAPTOPRIL
Sponsored by
Instituto Materno Infantil Prof. Fernando Figueira
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Preeclampsia focused on measuring captopril, clonidine, pregnancy-induced hypertension,

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Hypertensive disorders of pregnancy;
  • Postpartum;
  • Age 18 to 45 years;
  • Very high blood pressure

Exclusion Criteria:

  • Cardiac disease;
  • Smoking;
  • Use of illicit drugs that may interfere with maternal hemodynamics;
  • Contraindications to the use of captopril: renal failure, chronic liver disease and hypersensitivity to the drug;
  • Contraindications to the use of clonidine: sinus node disease, chronic liver disease and hypersensitivity to the drug;
  • Inability to receive postpartum oral medications

Sites / Locations

  • IMIP

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

CLONIDINE

CAPTOPRIL

Arm Description

Postpartum patients with very high blood pressure will be treated with oral clonidine (0,1mg)

Postpartum patients with very high blood pressure will be treated with oral CAPTOPRIL (25mg)

Outcomes

Primary Outcome Measures

Time until resolution of very high blood pressure episode
The time until resolution of very high blood pressure episode after clonidin or captopril use.

Secondary Outcome Measures

Maternal outcomes
Daily average systolic blood pressure;Daily average diastolic blood pressure;Need for combination with other hypotensive agent for the peak pressure or antihypertensive treatment maintenance;Need for new dose of antihypertensive medication for very high blood pressure; Laboratory tests during the postpartum; Adverse effects of hypotensive used for very high blood pressure;Puerperal complications

Full Information

First Posted
October 30, 2012
Last Updated
July 25, 2013
Sponsor
Instituto Materno Infantil Prof. Fernando Figueira
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1. Study Identification

Unique Protocol Identification Number
NCT01761916
Brief Title
Clonidine Versus Captopril for Treatment of Postpartum Very High Blood Pressure
Acronym
CLONCAP
Official Title
Randomized Clinical Trial for Effectiveness of Clonidine Versus Captopril for Treatment of Postpartum Very High Blood Pressure
Study Type
Interventional

2. Study Status

Record Verification Date
June 2013
Overall Recruitment Status
Completed
Study Start Date
January 2013 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
June 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Instituto Materno Infantil Prof. Fernando Figueira

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The postpartum period represents a stage of the pregnancy-puerperal still rarely addressed scientifically. There are no reports in the literature and concrete enough to elucidate important issues, especially in the field of hypertension and pregnancy. Searches based on current evidence concentrate their focus on the diagnosis of hypertensive disorders and treatment of these diseases maternofetais repercussions. However, the prognosis in the short and long term, as the BP outcome in mothers with severe preeclampsia, the most effective treatment for the control of hypertensive crisis and metabolic and cardiovascular events after two years of termination of pregnancy require further clarification. The main idea for developing this research came from the clinical experience with the use of captopril in Obstetric ICU IMIP. This drug has long been used in postpartum women with severe preeclampsia or chronic hypertension exacerbated by pregnancy for control of hypertensive crisis and keeping pressure levels. Following the technical standards of the institution and during his administration, there were reports of side effects such as dry cough and nausea, beyond the threshold dose of 150mg daily captopril was easily achieved hindering control the use of hypotensive. Alternative therapy, clonidine began to be used in mothers with some restriction on the use of ACE inhibitors and its hypotensive effect for peak pressure was satisfactory. What is not known yet is how long clonidine reduces high blood pressure and how long to leave stabilized compared to the use of captopril. There are no reports in the literature databases, no randomized clinical trials that prove the effectiveness of clonidine for the treatment of hypotensive pressure peaks in this particular group of patients, even in comparison with other classes of antihypertensive drugs, especially captopril, to this purpose. The investigators' primary assumption is that clonidine has better effectiveness in decreasing the frequency of pressure peaks when compared with captopril.
Detailed Description
The postpartum period represents a stage of the pregnancy-puerperal still rarely addressed scientifically. There are no reports in the literature and concrete enough to elucidate important issues, especially in the field of hypertension and pregnancy. Searches based on current evidence concentrate their focus on the diagnosis of hypertensive disorders and treatment of these diseases maternofetais repercussions. However, the prognosis in the short and long term, as the BP outcome in mothers with severe preeclampsia, the most effective treatment for the control of hypertensive crisis and metabolic and cardiovascular events after two years of termination of pregnancy require further clarification. The main idea for developing this research came from the clinical experience with the use of captopril in Obstetric ICU IMIP. This drug has long been used in postpartum women with severe preeclampsia or chronic hypertension exacerbated by pregnancy for control of hypertensive crisis and keeping pressure levels. Following the technical standards of the institution and during his administration, there were reports of side effects such as dry cough and nausea, beyond the threshold dose of 150mg daily captopril was easily achieved hindering control the use of hypotensive. Alternative therapy, clonidine began to be used in mothers with some restriction on the use of ACE inhibitors and its hypotensive effect for peak pressure was satisfactory. What is not known yet is how long clonidine reduces high blood pressure and how long to leave stabilized compared to the use of captopril. There are no reports in the literature databases, no randomized clinical trials that prove the effectiveness of clonidine for the treatment of hypotensive pressure peaks in this particular group of patients, even in comparison with other classes of antihypertensive drugs, especially captopril, to this purpose. The investigators' primary assumption is that clonidine has better effectiveness in decreasing the frequency of pressure peaks when compared with captopril. A triple blind randomized clinical trial will be conducted. Postpartum women with hypertensive disorders of pregnancy, admitted to the obstetric ICU of IMIP will be included in the research. After inclusion in the study, drugs for for very high blood pressure, according to randomization(captopril and clonidine)will be used. clonidine and captopril are administered at a dose of 25mg and 0.1mg respectively. If there is no control of blood pressure in 20 minutes new hypotensive doses will be administered until a total of 150mg/day (six tablets) and Captopril 0.6 mg / day (six tablets) clonidine. After exceeded the allowed dose, other drugs may be associated. Initially, nifedipine (30mg/day to 60mg/day) according to the service routine. The goal of intervention is to maintain a systolic blood pressure below 170mmHg and diastolic pressure below 110mmHg, with the lowest possible dose. Thus, these medications will be increased should the need arise, according to measurements taken daily by the attending physician and the nursing staff.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Preeclampsia
Keywords
captopril, clonidine, pregnancy-induced hypertension,

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CLONIDINE
Arm Type
Experimental
Arm Description
Postpartum patients with very high blood pressure will be treated with oral clonidine (0,1mg)
Arm Title
CAPTOPRIL
Arm Type
Active Comparator
Arm Description
Postpartum patients with very high blood pressure will be treated with oral CAPTOPRIL (25mg)
Intervention Type
Drug
Intervention Name(s)
CLONIDINE
Other Intervention Name(s)
CLON
Intervention Description
Postpartum patients with very high blood pressure will be treated with oral clonidine (0,1mg)
Intervention Type
Drug
Intervention Name(s)
CAPTOPRIL
Other Intervention Name(s)
CAP
Intervention Description
Postpartum patients with very high blood pressure will be treated with oral captopril (25mg)
Primary Outcome Measure Information:
Title
Time until resolution of very high blood pressure episode
Description
The time until resolution of very high blood pressure episode after clonidin or captopril use.
Time Frame
During hospital stay, up until one month postpartum
Secondary Outcome Measure Information:
Title
Maternal outcomes
Description
Daily average systolic blood pressure;Daily average diastolic blood pressure;Need for combination with other hypotensive agent for the peak pressure or antihypertensive treatment maintenance;Need for new dose of antihypertensive medication for very high blood pressure; Laboratory tests during the postpartum; Adverse effects of hypotensive used for very high blood pressure;Puerperal complications
Time Frame
During hospital stay, up until one month postpartum

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Hypertensive disorders of pregnancy; Postpartum; Age 18 to 45 years; Very high blood pressure Exclusion Criteria: Cardiac disease; Smoking; Use of illicit drugs that may interfere with maternal hemodynamics; Contraindications to the use of captopril: renal failure, chronic liver disease and hypersensitivity to the drug; Contraindications to the use of clonidine: sinus node disease, chronic liver disease and hypersensitivity to the drug; Inability to receive postpartum oral medications
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carlos Noronha, MD
Organizational Affiliation
IMIP
Official's Role
Principal Investigator
Facility Information:
Facility Name
IMIP
City
Recife
State/Province
Pernambuco
ZIP/Postal Code
50070-550
Country
Brazil

12. IPD Sharing Statement

Citations:
PubMed Identifier
28125624
Citation
Noronha Neto C C, Maia SS, Katz L, Coutinho IC, Souza AR, Amorim MM. Clonidine versus Captopril for Severe Postpartum Hypertension: A Randomized Controlled Trial. PLoS One. 2017 Jan 26;12(1):e0168124. doi: 10.1371/journal.pone.0168124. eCollection 2017.
Results Reference
derived
PubMed Identifier
23899372
Citation
Noronha-Neto C, Katz L, Coutinho IC, Maia SB, Souza AS, Amorim MM. Clonidine versus captopril for treatment of postpartum very high blood pressure: study protocol for a randomized controlled trial (CLONCAP). Reprod Health. 2013 Jul 30;10:37. doi: 10.1186/1742-4755-10-37.
Results Reference
derived

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Clonidine Versus Captopril for Treatment of Postpartum Very High Blood Pressure

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