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Effects of Viagra on Heart Function in Patients With Heart Failure

Single Dose Sildenafil in Heart Failure Patients Improves 6-minute Walk Test by a Reduction in Left Ventricular Filling Pressure

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00781508
Enrollment
10
Registered
2008-10-29
Start date
2006-12-31
Completion date
2009-11-30
Last updated
2014-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure, Left Ventricular Dysfunction

Keywords

heart failure, left sided, ventricular dysfunction, diastolic dysfunction, sildenafil

Brief summary

Sildenafil (Viagra) is known to reduce pulmonary hypertension. Heart failure patients also have pulmonary hypertension and several recent reports have shown that sildenafil leads to an improvement in their exercise capacity. In these studies sildenafil caused a reduction in the pulmonary and systemic vascular resistances, improved pulmonary gas diffusion and perhaps increased cardiac output. It is uncertain if left ventricular filling pressures are reduced and whether there is improvement in left ventricular relaxation. The investigators hypothesize that in heart failure patients the improvement in exercise capacity associated with sildenafil is related to a significant reduction in left ventricular filling pressures. The investigators propose to study 20 patients with stable but moderately symptomatic heart failure. The study design is a randomized cross-over trial of the administration of a single dose of sildenafil 50 mg or a matching placebo. Exercise capacity will be determined before and after the oral administration of sildenafil 50 mg or placebo. Left ventricular filling pressures will be assessed by Doppler echocardiography and the serum level of B-type natriuretic peptide (BNP is known to increase with higher left ventricular filling pressures). After an initial echocardiogram and performing a 6 minute walk test, the patient will then be given either sildenafil or a matching placebo in a randomized double-blind fashion. One hr later a blood sample for serum BNP, the echocardiogram and the 6 minute walk test will be repeated.

Detailed description

Sildenafil (Viagra) has been extensively studied in patients with idiopathic pulmonary hypertension. It reduces pulmonary vascular resistance, improves exercise capacity and is now an approved therapy for this condition. Heart failure (HF) patients also have pulmonary hypertension and several recent reports have shown that sildenafil leads to an improvement in their exercise capacity. In HF sildenafil causes a reduction in the pulmonary and systemic vascular resistances, improves pulmonary gas diffusion and perhaps increases cardiac output. It is uncertain if left ventricular filling pressures are reduced and whether there is improvement in left ventricular relaxation. We hypothesize that in HF patients the improvement in exercise capacity associated with sildenafil is related to a significant reduction in left ventricular filling pressures. We propose to study 10 patients with stable, symptomatic HF Class III. The study design is a randomized cross-over assignment of the administration of a single oral dose of sildenafil 50 mg or a matching placebo. Patients will be excluded if walking is impaired due to non-cardiac conditions or if they are taking nitrates. Exercise capacity will be determined before and 60 minutes after the oral administration of sildenafil 50 mg or placebo. The difference in the standardized 6 minute walk test (distance patient is able to walk over a 6 minute interval) will be used to assess exercise capacity. Left ventricular filling pressures will be assessed by Doppler echocardiography and the serum level of B-type natriuretic peptide (BNP). Evaluation of left ventricular relaxation will be determined by Doppler echocardiography techniques. Each patient will have a blood sample for BNP, an initial echocardiogram and perform a 6 minute walk test. They will then be given a single dose of either sildenafil or a matching placebo in a randomized double-blind fashion. The randomization was performed so that half of the group would receive the placebo on the initial test and sildenafil on the subsequent test and the other half would have the reverse sequence. One hr after the medication/placebo administration a blood sample for serum BNP, the echocardiogram and the 6 minute walk test will be repeated. After completion of the above protocol, the patient will return in 48 hrs and the protocol will be repeated with the predetermined assignment of either placebo or sildenafil.

Interventions

DRUGsildenafil

Changes in left ventricular filling pressure 1 hour after the administration of a single oral dose of sildenafil 50 mg.

OTHERPlacebo

Changes in left ventricular filling pressure 1 hour after oral administration of placebo

Sponsors

National Center for Research Resources (NCRR)
CollaboratorNIH
MetroHealth Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
25 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Adults with Class III congestive heart failure and impaired left ventricular systolic function. * A prior BNP level ≥ 200 pg/mL. * Previously documented systolic pulmonary artery pressure \>40 mmHg. * Clinically stable for a minimum of 6 weeks. * Able to give informed consent,

Exclusion criteria

* Unable to give informed consent. * Currently taking nitrates. * A HF exacerbation within the past 6 weeks. * Co-morbid conditions that could limit their walking. * Have a resting systolic blood pressure \< 110 mmHg

Design outcomes

Primary

MeasureTime frameDescription
Reduction of the Left Ventricular Filling Pressure in Association With Administration of SildenafilLeft ventricular filling pressure was assessed 1 hr after oral administration of sildenafilLeft ventricular filling pressure was assessed by the ratio of the velocity of early mitral inflow (E) divided by the early tissue velocity (e). E/e

Secondary

MeasureTime frameDescription
The Distance Walked During the 6-minute Walk Test 1 hr After the Oral Administration of Sildenafil 50 mg.Measured 1 hr after oral administration of sildenafil 50 mgA standardized course was used to determine the distance walked (meters) during a 6 min walk supervised by a nurse trained in performance of the test.

Countries

United States

Participant flow

Recruitment details

Patients were recruited from the Heart Failure Clinic at MetroHealth Medical Center over a 12 month interval. Recruitment was slow due to the fact that many of the patients were already perscirbed nitrates and so were ineligible for the study.

Pre-assignment details

More than 50 patients had to be excluded due to their already taking nitrates for their heart failure.

Participants by arm

ArmCount
Sildenafil First Placebo Second
Effect of sildenafil on left ventricular filling pressures in patients with heart failure
5
Placebo First Sildenafil Second
Effect of placebo on left ventricular filling pressures in patients with heart failure
5
Total10

Baseline characteristics

CharacteristicPlacebo First Sildenafil SecondSildenafil First Placebo SecondTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
2 Participants1 Participants3 Participants
Age, Categorical
Between 18 and 65 years
3 Participants4 Participants7 Participants
Age, Continuous64 years
STANDARD_DEVIATION 12
64 years
STANDARD_DEVIATION 12
64 years
STANDARD_DEVIATION 12
Region of Enrollment
United States
5 participants5 participants10 participants
Sex: Female, Male
Female
0 Participants1 Participants1 Participants
Sex: Female, Male
Male
5 Participants4 Participants9 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 50 / 5
serious
Total, serious adverse events
0 / 50 / 5

Outcome results

Primary

Reduction of the Left Ventricular Filling Pressure in Association With Administration of Sildenafil

Left ventricular filling pressure was assessed by the ratio of the velocity of early mitral inflow (E) divided by the early tissue velocity (e). E/e

Time frame: Left ventricular filling pressure was assessed 1 hr after oral administration of sildenafil

Population: All patients (10) that completed the protocol were analyzed.

ArmMeasureValue (MEAN)Dispersion
Sildenafil First Then PlaceboReduction of the Left Ventricular Filling Pressure in Association With Administration of Sildenafil16.7 E/e' ratioStandard Deviation 6.9
Placebo First Then SildenafilReduction of the Left Ventricular Filling Pressure in Association With Administration of Sildenafil16.4 E/e' ratioStandard Deviation 6.5
Secondary

The Distance Walked During the 6-minute Walk Test 1 hr After the Oral Administration of Sildenafil 50 mg.

A standardized course was used to determine the distance walked (meters) during a 6 min walk supervised by a nurse trained in performance of the test.

Time frame: Measured 1 hr after oral administration of sildenafil 50 mg

ArmMeasureValue (MEAN)Dispersion
Sildenafil First Then PlaceboThe Distance Walked During the 6-minute Walk Test 1 hr After the Oral Administration of Sildenafil 50 mg.210 metersStandard Deviation 34
Placebo First Then SildenafilThe Distance Walked During the 6-minute Walk Test 1 hr After the Oral Administration of Sildenafil 50 mg.219 metersStandard Deviation 40

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026