Intracavernosal Injection of Papaverine/Verapamil Versus Papaverine/Phentolamine in Erectile Dysfunction

A

Adam International Hospital

Status

Completed

Conditions

Erectile Dysfunction

Treatments

Drug: Verapamil

Study type

Observational

Funder types

Other

Identifiers

NCT03033537
2016

Details and patient eligibility

About

Introduction: Erectile dysfunction is a common condition with a significant effect on quality of life. Verapamil is calcium channel blocker of the phenyl alkylamine class which relaxes the tone of the smooth muscles lining blood vessels, leading to their dilatation.

Full description

Objective: Evaluating the effect of intracavernosal injection of (Papaverine + Verapamil) and comparing it with (Papaverine + Phentolamine) in patients with erectile dysfunction. Patients and methods: Each one of the 20 erectile dysfunction patients was subjected to intracavernosal injection with (30mg Papaverine + 1mg Phentolamine), where penile duplex & clinical evaluation was carried out followed by a wash out interval of 2 weeks after which each patient was subjected to the exact previous procedures using (30 mg Papaverine + 5 mg Verapamil). Keywords: Erectile dysfunction - Intracavernosal injection - Penile duplex - Phentolamine - Verapamil.

Enrollment

20 patients

Sex

Male

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Married male patients suffering from erectile dysfunction and scheduled for intracavernosal injection.

Exclusion criteria

Responders to PDE5-inhibitors; congenital or acquired penile anomalies; uncontrolled medical conditions or known hypersensitivity to verapamil; Peyronie's disease and any known bleeding or coagulation disorders.

Trial design

20 participants in 2 patient groups

Verapamil
Description:
Intracavernosal injection of Verapamil
Treatment:
Drug: Verapamil
Phentolamine
Description:
Intracavernosal injection of Phentolamine to treat erectile dysfunction for a period of 2 wweks
Treatment:
Drug: Verapamil

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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