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Sildenafil for Secondary Pulmonary Hypertension Due to Valvular Disease (SIOVAC)

Primary Purpose

Pulmonary Hypertension, Valvular Heart Disease

Status
Completed
Phase
Phase 4
Locations
Spain
Study Type
Interventional
Intervention
Sildenafil Citrate
Placebo
Sponsored by
Hospital General Universitario Gregorio Marañon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pulmonary Hypertension focused on measuring Secondary Pulmonary Hypertension, Valvular Heart Disease, Phosphodiesterase-Inhibitors, Sildenafil, Outcomes Research

Eligibility Criteria

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

Inclusion Criteria:

  • Age at the date of selection ≥ 18 years
  • Mean pulmonary pressure ≥ 30 mmHg, measured by a Swan-Ganz catheter placed in the pulmonary artery
  • Heart valve intervention: surgical or percutaneous replacement, repair or dilatation performed at least one year before inclusion
  • Stable clinical condition for at least one month, without hospital admissions for heart failure, and on appropriate and stable doses of conventional cardiovascular medications

Exclusion Criteria:

  • Requiring or likely to require the following medications: organic nitrates, alpha-blocker therapy, potent cytochrome P450 3A4 inhibitors (erythromycin, ketoconazole, cimetidine, HIV protease inhibitors such ritonavir and saquinavir) Patients who have suffered a myocardial infarction, stroke, or life-threatening arrhythmia within the last 6 months.
  • Patients with resting hypotension, with systolic blood pressure < 90 mmHg
  • Patients with retinitis pigmentosa
  • Anatomical deformation of the penis (such as angulation, cavernosal fibrosis or Peyronie's disease) or patients who have conditions which may predispose them to priapism (such as sickle cell anemia, multiple myeloma, or leukemia)
  • Severe renal impairment with creatinine clearance < 30 ml/min
  • Significant hepatic dysfunction
  • Prosthesis or valvular dysfunction with hemodynamic repercussion.
  • Pregnant or breast-feeding women
  • Patients unlikely to cooperate in the study or with inability or unwillingness to give informed consent
  • Life expectancy less than 2 years due to non-cardiac disease

Sites / Locations

  • Hospital Universitario Santiago de Compostela
  • Hospital Universitario Alava
  • Hospital German Trias y Pujol
  • Hospital de la Santa Creu y San Pau
  • Hospital Fundación de Alcorcón
  • Hospital Puerta de Hierro
  • Hospital de Galdakao
  • Hospital Reina Sofía
  • Hospital Virgen de las Nieves
  • Hospital Juan Canalejo
  • Hospital de Leon
  • Hospital General Universitario Gregorio Maranon
  • Hospital 12 de Octubre
  • Hospital Infanta Leonor
  • Hospital Virgen de la Victoria
  • Hospital Universitario de Salamanca
  • Hospital Universitario de Canarias
  • Hospital Clínico de Valladolid

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Sildenafil Citrate

Placebo

Arm Description

Sildenafil Citrate 40 mg t.i.d. oral

Sildenafil-matched oral placebo 40 mg t.i.d

Outcomes

Primary Outcome Measures

Combined Outcome End-Point: all-cause mortality or hospital admission for heart failure, worsening of World Health Organization (WHO) functional class, or of the patient global assessment score

Secondary Outcome Measures

Change from baseline to the sixth month in the in the six-minute walk test
Change on WHO functional capacity
All cause mortality
Cardiovascular mortality
Number of hospital admissions caused by or related to heart failure in each patient
Rate of progression/regression of tricuspid regurgitation by Doppler-echocardiography
Change on right ventricular (RV) dimensions and function assessed by Doppler echocardiography
Change on RV volumes and function assessed by cardiac magnetic resonance
Change on the right catheterization hemodynamic parameters
Identify patients who are more likely to respond to therapy by pharmacogenetics analysis

Full Information

First Posted
March 13, 2009
Last Updated
September 22, 2016
Sponsor
Hospital General Universitario Gregorio Marañon
Collaborators
Instituto de Salud Carlos III, Fundación de Investigación en Red en Enfermedades Cardiovasculares
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1. Study Identification

Unique Protocol Identification Number
NCT00862043
Brief Title
Sildenafil for Secondary Pulmonary Hypertension Due to Valvular Disease
Acronym
SIOVAC
Official Title
Sildenafil for Improving Outcomes After Valvular Correction
Study Type
Interventional

2. Study Status

Record Verification Date
September 2016
Overall Recruitment Status
Completed
Study Start Date
April 2009 (undefined)
Primary Completion Date
July 2016 (Actual)
Study Completion Date
July 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital General Universitario Gregorio Marañon
Collaborators
Instituto de Salud Carlos III, Fundación de Investigación en Red en Enfermedades Cardiovasculares

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate the clinical efficacy of the mid-term treatment with sildenafil in patients with persistent moderate or severe pulmonary hypertension (PH) after a heart valve intervention.
Detailed Description
Phase IV, prospective, multicenter, randomized, double-blind, placebo-controlled, academically funded clinical trial, with 6 months follow-up. A total of 354 patients will be recruited. Inclusion criteria are: 1) successful surgical or percutaneous repair of a cardiac valve at least one year before screening and 2) persistent moderate or severe PH, and 3) absence of any residual significant valvular lesion. Patients will be randomized 1:1 to received sildenafil 40 mg t.i.d. or placebo. The primary endpoint is a clinical composite score combining: all-cause mortality, hospital admission for heart failure, World Health Organization (WHO) functional class, and the patient global assessment score. Additional clinical and mechanistic secondary end-points are defined.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Hypertension, Valvular Heart Disease
Keywords
Secondary Pulmonary Hypertension, Valvular Heart Disease, Phosphodiesterase-Inhibitors, Sildenafil, Outcomes Research

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sildenafil Citrate
Arm Type
Experimental
Arm Description
Sildenafil Citrate 40 mg t.i.d. oral
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Sildenafil-matched oral placebo 40 mg t.i.d
Intervention Type
Drug
Intervention Name(s)
Sildenafil Citrate
Intervention Description
40 mg t.i.d.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo t.i.d.
Primary Outcome Measure Information:
Title
Combined Outcome End-Point: all-cause mortality or hospital admission for heart failure, worsening of World Health Organization (WHO) functional class, or of the patient global assessment score
Time Frame
Six months
Secondary Outcome Measure Information:
Title
Change from baseline to the sixth month in the in the six-minute walk test
Time Frame
6 Months
Title
Change on WHO functional capacity
Time Frame
3 & 6 Months
Title
All cause mortality
Time Frame
6 Months
Title
Cardiovascular mortality
Time Frame
6 months
Title
Number of hospital admissions caused by or related to heart failure in each patient
Time Frame
6 months
Title
Rate of progression/regression of tricuspid regurgitation by Doppler-echocardiography
Time Frame
3 & 6 Months
Title
Change on right ventricular (RV) dimensions and function assessed by Doppler echocardiography
Time Frame
3 & 6 months
Title
Change on RV volumes and function assessed by cardiac magnetic resonance
Time Frame
6 Months
Title
Change on the right catheterization hemodynamic parameters
Time Frame
6 Months
Title
Identify patients who are more likely to respond to therapy by pharmacogenetics analysis
Time Frame
6 Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age at the date of selection ≥ 18 years Mean pulmonary pressure ≥ 30 mmHg, measured by a Swan-Ganz catheter placed in the pulmonary artery Heart valve intervention: surgical or percutaneous replacement, repair or dilatation performed at least one year before inclusion Stable clinical condition for at least one month, without hospital admissions for heart failure, and on appropriate and stable doses of conventional cardiovascular medications Exclusion Criteria: Requiring or likely to require the following medications: organic nitrates, alpha-blocker therapy, potent cytochrome P450 3A4 inhibitors (erythromycin, ketoconazole, cimetidine, HIV protease inhibitors such ritonavir and saquinavir) Patients who have suffered a myocardial infarction, stroke, or life-threatening arrhythmia within the last 6 months. Patients with resting hypotension, with systolic blood pressure < 90 mmHg Patients with retinitis pigmentosa Anatomical deformation of the penis (such as angulation, cavernosal fibrosis or Peyronie's disease) or patients who have conditions which may predispose them to priapism (such as sickle cell anemia, multiple myeloma, or leukemia) Severe renal impairment with creatinine clearance < 30 ml/min Significant hepatic dysfunction Prosthesis or valvular dysfunction with hemodynamic repercussion. Pregnant or breast-feeding women Patients unlikely to cooperate in the study or with inability or unwillingness to give informed consent Life expectancy less than 2 years due to non-cardiac disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Javier Bermejo, MD, PhD
Organizational Affiliation
Hospital General Universitario Gregorio Maranon
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Universitario Santiago de Compostela
City
Santiago de Compostela
State/Province
A Coruña
Country
Spain
Facility Name
Hospital Universitario Alava
City
Vitoria
State/Province
Alava
Country
Spain
Facility Name
Hospital German Trias y Pujol
City
Badalona
State/Province
Barcelona
Country
Spain
Facility Name
Hospital de la Santa Creu y San Pau
City
Barcelona
State/Province
Barcelon
Country
Spain
Facility Name
Hospital Fundación de Alcorcón
City
Alcorcón
State/Province
Madrid
Country
Spain
Facility Name
Hospital Puerta de Hierro
City
Majadahonda
State/Province
Madrid
Country
Spain
Facility Name
Hospital de Galdakao
City
Galdakao
State/Province
Vizcaya
Country
Spain
Facility Name
Hospital Reina Sofía
City
Córdoba
Country
Spain
Facility Name
Hospital Virgen de las Nieves
City
Granada
Country
Spain
Facility Name
Hospital Juan Canalejo
City
La Coruna
Country
Spain
Facility Name
Hospital de Leon
City
Leon
Country
Spain
Facility Name
Hospital General Universitario Gregorio Maranon
City
Madrid
ZIP/Postal Code
28007
Country
Spain
Facility Name
Hospital 12 de Octubre
City
Madrid
Country
Spain
Facility Name
Hospital Infanta Leonor
City
Madrid
Country
Spain
Facility Name
Hospital Virgen de la Victoria
City
Malaga
Country
Spain
Facility Name
Hospital Universitario de Salamanca
City
Salamanca
Country
Spain
Facility Name
Hospital Universitario de Canarias
City
Tenerife
Country
Spain
Facility Name
Hospital Clínico de Valladolid
City
Valladolid
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
33399006
Citation
Bermejo J, Gonzalez-Mansilla A, Mombiela T, Fernandez AI, Martinez-Legazpi P, Yotti R, Garcia-Orta R, Sanchez-Fernandez PL, Castano M, Segovia-Cubero J, Escribano-Subias P, Alberto San Roman J, Borras X, Alonso-Gomez A, Botas J, Crespo-Leiro MG, Velasco S, Bayes-Genis A, Lopez A, Munoz-Aguilera R, Jimenez-Navarro M, Gonzalez-Juanatey JR, Evangelista A, Elizaga J, Martin-Moreiras J, Gonzalez-Santos JM, Moreno-Escobar E, Fernandez-Aviles F; SIOVAC ("Sildenafil for Improving Outcomes after VAlvular Correction") Investigators. Persistent Pulmonary Hypertension in Corrected Valvular Heart Disease: Hemodynamic Insights and Long-Term Survival. J Am Heart Assoc. 2021 Jan 19;10(2):e019949. doi: 10.1161/JAHA.120.019949. Epub 2021 Jan 5.
Results Reference
derived
PubMed Identifier
29281101
Citation
Bermejo J, Yotti R, Garcia-Orta R, Sanchez-Fernandez PL, Castano M, Segovia-Cubero J, Escribano-Subias P, San Roman JA, Borras X, Alonso-Gomez A, Botas J, Crespo-Leiro MG, Velasco S, Bayes-Genis A, Lopez A, Munoz-Aguilera R, de Teresa E, Gonzalez-Juanatey JR, Evangelista A, Mombiela T, Gonzalez-Mansilla A, Elizaga J, Martin-Moreiras J, Gonzalez-Santos JM, Moreno-Escobar E, Fernandez-Aviles F; Sildenafil for Improving Outcomes after VAlvular Correction (SIOVAC) investigators. Sildenafil for improving outcomes in patients with corrected valvular heart disease and persistent pulmonary hypertension: a multicenter, double-blind, randomized clinical trial. Eur Heart J. 2018 Apr 14;39(15):1255-1264. doi: 10.1093/eurheartj/ehx700.
Results Reference
derived
Links:
URL
http://www.mineco.gob.es
Description
Funding Agent
URL
http://www.redcardiovascular.com
Description
Cardiovascular Research Spanish National Network

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Sildenafil for Secondary Pulmonary Hypertension Due to Valvular Disease

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