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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03763045
Other study ID # Med135
Secondary ID
Status Active, not recruiting
Phase Phase 2/Phase 3
First received
Last updated
Start date December 2, 2018
Est. completion date February 28, 2019

Study information

Verified date January 2019
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Sildenafil is a phosphodiesterase inhibitor that can exert a nitric oxide-mediated vasodilation effect, so it's considered one of the preferred agents especially in hypoxia induced pulmonary hypertension, can achieve pulmonary vasodilation by enhancing sustained levels of cyclic guanosine monophosphate (cGMP) and nitric oxide.

Despite the potential burden of pulmonary hypertension in hemodialysis patients, such agent like sildenafil has limited studies about optimum dose, safety and long term efficacy in End stage renal disease patients on hemodialysis with pulmonary hypertension


Description:

1- To evaluate the effect of sildenafil on pulmonary artery pressure and right ventricular function in hemodialysis patients with pulmonary hypertension.

1. Primary outcome:

● Reduction in estimated Pulmonary Artery pressure value (ePAP) in mmHg via transthoracic Doppler Echocardiography.

2. Secondary outcomes:

- Detection of safety of sildenafil in hemodialysis patients.

- Finding out sildenafil's optimum dose for hemodialysis patients with pulmonary hypertension.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 60
Est. completion date February 28, 2019
Est. primary completion date February 16, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

1. Age from 18-80 years old.

2. Patients on maintenance hemodialysis for more than six months receiving 3 sessions / week using bicarbonate dialysate with a low flux filter and heparin as anticoagulant.

3. Estimated Pulmonary Artery Pressure (ePAP) =35 mmHg via Doppler echocardiography

4. Urea reduction ratio (URR) will be = 60% for all patients.

5. Dry weight will be targeted in each case to achieve edema-free state.

6. Informed consent in accordance with the Declaration of Helsinki.

Exclusion Criteria:

- 1. Current treatment of pulmonary hypertension (prostacyclin analogues, endothelin receptor antagonists or phosphodiesterase inhibitors).

2-Heart diseases (congestive heart failure, ischemic heart disease, congenital heart disease).

3- Lung diseases (chronic obstructive pulmonary disease, pulmonary thromboemboli or tumor, interstitial lung diseases, sleep apnea, pulmonary fibrosis, Sarcoidosis).

4-Systemic diseases (scleroderma, systemic lupus erythematosus, portal hypertension).

5-Human immunodeficiency virus (HIV) infection. 6-History of hypersensitivity to sildenafil. 7-Treatment with any drugs that may interact with sildenafil (Erythromycin , Azoles, Saquinavir-CYP3A4 inhibitors- , Bosentan - CYP3A4 inducer-Nitrates ) 8- Uncontrolled hypertension 9- Anemia with hemoglobin level <10 g/dl

Study Design


Intervention

Drug:
Sildenafil
Sildenafil 25 mg: Phosphodiesterase inhibitor to be taken once daily
Sildenafil
Sildenafil 50 mg: Phosphodiesterase inhibitor to be taken once daily
Other:
Placebo
Placebo tablet.

Locations

Country Name City State
Egypt Ain Shams University Hospital Cairo Abbasia

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Decrease in Pulmonary Artery Pressure Decrease in ePAP (mmHg) via Doppler echocardiography Systolic right ventricular (or pulmonary artery) 3 months
Secondary Transthoracic echocardiography Decrease in Estimated PASP (Pulmonary Artery Systolic Pressure) in (mmHg). 3 months
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