NCT00667966 - Assess Efficacy in Subjects With Traumatic Spinal Cord Injury | Biotech Hunter

Enrollment

Participants

Timeline

Start Date

July 31, 2005

Study Completion Date

February 28, 2007

Conditions

Erectile DysfunctionSpinal Cord Injury

Interventions

DRUG

Vardenafil (Levitra, BAY 38-9456), 10 mg

10 mg vardenafil was administered with a glass of water 1 h before starting the test with the stimulator.

DRUG

Placebo

10/20 mg placebo in sequence in respective arm

DRUG

Vardenafil (Levitra, BAY 38-9456), 20 mg

20 mg vardenafil was administered with a glass of water 1 h before starting the test with the stimulator.

Trial Locations (2)

Toledo

Badalona