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Resistant Hypertension Optimal Treatment (ReHOT)

Primary Purpose

Hypertension

Status
Unknown status
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Spironolactone
Clonidine
Sponsored by
Instituto do Coracao
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypertension focused on measuring Resistant Hypertension

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria

  1. Patients aged between 18 and 75
  2. With systolic blood pressure> 160 mmHg and <220mmHg and / or diastolic> 100 mmHg in the sitting position and according to Brazilian Guidelines on Hypertension (perform steps by obtaining two consecutive measurements differing by less than 4 mmHg between them, calibrated using a sphygmomanometer)
  3. Patient regularly enrolled in participating center

Exclusion criteria

  1. Systolic blood pressure> 220 mmHg
  2. Patients with cardiovascular events (stroke, AMI, etc.). or cardiovascular procedures with less than 6 months of evolution
  3. Renal stages IV and V (glomerular20 filtration estimated by MDRD formula <30 ml / min; where MDRD = 186 x (S_Cr) -1.154 x (age) -0.203 x (0.742 if fem.) x (1.210 if Afro-amer. ))
  4. Heart failure class III and IV
  5. History of malignant disease with life expectancy < 2 years
  6. Alcoholism
  7. Psychiatric illnesses that prevent compliance with the Protocol
  8. Women of childbearing age who are not in use of effective contraception
  9. Pregnancy
  10. Arrhythmias, valvular heart disease, AV block 2 and 3 degrees without MP
  11. Hepatic impairment
  12. Patients with a history of hypersensitivity to any of the drugs under study
  13. Examination of the fundus: Grade III and Grade IV

Sites / Locations

  • University of São Paulo General HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Spironolactone

Clonidine

Arm Description

Outcomes

Primary Outcome Measures

Blood pressure (mmHg)
Compare the effect of spironolactone on blood pressure vs. clonidine, when added to a multidrug combination consisting of chlorthalidone plus ACEi (or ARB) plus amlodipine, all of 3 up-titrated to the highest dose;

Secondary Outcome Measures

Sympathetic nervous system and renin-angiotensin-aldosterone activity
Compare the role of measuring sympathetic nervous system activity and renin-angiotensin-aldosterone activity on predicting the response of blood pressure to spironolactone and clonidine.

Full Information

First Posted
July 11, 2012
Last Updated
June 6, 2013
Sponsor
Instituto do Coracao
Collaborators
Conselho Nacional de Desenvolvimento Científico e Tecnológico
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1. Study Identification

Unique Protocol Identification Number
NCT01643434
Brief Title
Resistant Hypertension Optimal Treatment
Acronym
ReHOT
Official Title
Multicenter Study of Patients With Hypertension Resistant to Patient Identification and Standardization of Therapeutic
Study Type
Interventional

2. Study Status

Record Verification Date
June 2013
Overall Recruitment Status
Unknown status
Study Start Date
August 2012 (undefined)
Primary Completion Date
December 2013 (Anticipated)
Study Completion Date
July 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Instituto do Coracao
Collaborators
Conselho Nacional de Desenvolvimento Científico e Tecnológico

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Resistant hypertension (ReHy) is an emerging clinical and public health problem which tends to increase because populations are living longer and there is a growing global epidemic of obesity, diabetes and sleep apnea. It is also tempting to speculate that the excessive dietary salt ingestion reported in many countries can contribute substantially to the risk of ReHy development. ReHy is defined as persistent high blood pressure (above the target goal) in spite of the use of at least 3 antihypertensive agents of different classes, one of them must being diuretics. Data regarding the exact prevalence of ReHy are very limited. In addition, little data is available about 3-drug combinations but a simplified treatment algorithm has demonstrated that a combination of a diuretic plus an angiotensin-converting enzyme inhibitors (ACEi) or an angiotensin-receptor blocker (ARB) plus diuretic, adding a calcium channel blocker when necessary, controlled 64% of hypertensive patients and, in addition, was even more efficient than the current guideline-based management. By contrast, the fourth drug to be added-on the triple regimen is still controversial and guided by empirical choices or personal preferences. Recent studies suggest the emerging role of spironolactone as the "first-line" fourth drug for treating resistant hypertension. Conversely, because of the pathophysiological rationale, others have proposed the use of β-blockers or even centrally acting agents for managing the sympathetic hyperactivity. The present concerns about the limited blood pressure reducing effect of β-blockers, especially in elderly people, the potent effect of centrally acting agents and our personal experience are pointing to clonidine as the fourth drug to be added-on to a multidrug combination for reaching optimal blood pressure in patients with ReHy. Nevertheless, no studies have been performed comparing, head-to-head, which one is the best fourth drug (spironolactone or clonidine) to be added-on to a common used multidrug combination in order to treat this condition. Therefore, the principal objectives of the ReHOT Trial are to assess prospectively: (1) the prevalence of ReHy in a cohort of outpatients with stage II hypertension; (2) the effect of spironolactone on blood pressure, in comparison to clonidine, when added to a multidrug combination consisting of chlorthalidone plus ACEi (or ARB) plus amlodipine, all of 3 up-titrated to the highest dose; (3) the role of measuring sympathetic nervous system activity and renin-angiotensin-aldosterone activity on predicting the response of blood pressure to spironolactone and clonidine.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension
Keywords
Resistant Hypertension

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Spironolactone
Arm Type
Active Comparator
Arm Title
Clonidine
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Spironolactone
Intervention Description
Spironolactone (titrating dose from 12.5 to 50mg SID)
Intervention Type
Drug
Intervention Name(s)
Clonidine
Intervention Description
Clonidine (titrating dose from 0.100-0.300mg BID)
Primary Outcome Measure Information:
Title
Blood pressure (mmHg)
Description
Compare the effect of spironolactone on blood pressure vs. clonidine, when added to a multidrug combination consisting of chlorthalidone plus ACEi (or ARB) plus amlodipine, all of 3 up-titrated to the highest dose;
Time Frame
Patients willl be followed for an expected average of 3 months
Secondary Outcome Measure Information:
Title
Sympathetic nervous system and renin-angiotensin-aldosterone activity
Description
Compare the role of measuring sympathetic nervous system activity and renin-angiotensin-aldosterone activity on predicting the response of blood pressure to spironolactone and clonidine.
Time Frame
At baseline and at the end of the randomization (3 months)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Patients aged between 18 and 75 With systolic blood pressure> 160 mmHg and <220mmHg and / or diastolic> 100 mmHg in the sitting position and according to Brazilian Guidelines on Hypertension (perform steps by obtaining two consecutive measurements differing by less than 4 mmHg between them, calibrated using a sphygmomanometer) Patient regularly enrolled in participating center Exclusion criteria Systolic blood pressure> 220 mmHg Patients with cardiovascular events (stroke, AMI, etc.). or cardiovascular procedures with less than 6 months of evolution Renal stages IV and V (glomerular20 filtration estimated by MDRD formula <30 ml / min; where MDRD = 186 x (S_Cr) -1.154 x (age) -0.203 x (0.742 if fem.) x (1.210 if Afro-amer. )) Heart failure class III and IV History of malignant disease with life expectancy < 2 years Alcoholism Psychiatric illnesses that prevent compliance with the Protocol Women of childbearing age who are not in use of effective contraception Pregnancy Arrhythmias, valvular heart disease, AV block 2 and 3 degrees without MP Hepatic impairment Patients with a history of hypersensitivity to any of the drugs under study Examination of the fundus: Grade III and Grade IV
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Eduardo M. Krieger, Doctor
Phone
+55113069 5048
Email
edkrieger@incor.usp.br
First Name & Middle Initial & Last Name or Official Title & Degree
Jose E. Krieger, Doctor
Phone
+55113069-5068
Email
zecakrieger@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eduardo M. Krieger, Doctor
Organizational Affiliation
University of São Paulo General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of São Paulo General Hospital
City
São Paulo
ZIP/Postal Code
05403-000
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eduardo M. krieger, Doctor
Phone
+55113069-5048
Email
edkrieger@incor.usp.br
First Name & Middle Initial & Last Name & Degree
Jose E. krieger, Doctor
Phone
+55113069 5068
Email
zecakrieger@gmail.com
First Name & Middle Initial & Last Name & Degree
Eduardo M. Krieger, Doctor

12. IPD Sharing Statement

Citations:
PubMed Identifier
29463627
Citation
Krieger EM, Drager LF, Giorgi DMA, Pereira AC, Barreto-Filho JAS, Nogueira AR, Mill JG, Lotufo PA, Amodeo C, Batista MC, Bodanese LC, Carvalho ACC, Castro I, Chaves H, Costa EAS, Feitosa GS, Franco RJS, Fuchs FD, Guimaraes AC, Jardim PC, Machado CA, Magalhaes ME, Mion D Jr, Nascimento RM, Nobre F, Nobrega AC, Ribeiro ALP, Rodrigues-Sobrinho CR, Sanjuliani AF, Teixeira MDCB, Krieger JE; ReHOT Investigators. Spironolactone Versus Clonidine as a Fourth-Drug Therapy for Resistant Hypertension: The ReHOT Randomized Study (Resistant Hypertension Optimal Treatment). Hypertension. 2018 Apr;71(4):681-690. doi: 10.1161/HYPERTENSIONAHA.117.10662. Epub 2018 Feb 20.
Results Reference
derived
PubMed Identifier
24338935
Citation
ReHOT Investigators; Krieger EM, Drager LF, Giorgi DM, Krieger JE, Pereira AC, Barreto-Filho JA, da Rocha Nogueira A, Mill JG. Resistant hypertension optimal treatment trial: a randomized controlled trial. Clin Cardiol. 2014 Jan;37(1):1-6. doi: 10.1002/clc.22228. Epub 2013 Dec 11. Erratum In: Clin Cardiol. 2014 Jun;37(6):388. Multiple investigator names added.
Results Reference
derived

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Resistant Hypertension Optimal Treatment

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