H-22411: BOTOX® for Peyronie's Disease



Status:Recruiting
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:February 2009
End Date:January 2017
Contact:Sharon Harrison
Email:sharons@bcm.edu
Phone:713-798-2240

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The Efficacy of Botulinum Toxin Type a in Treating Peyronie's Disease

Peyronie's disease is a condition in which a plaque, or hard lump, forms on the penis. It
causes hardened tissue, pain, and an abnormal bending in the penis. These symptoms are more
severe during an erection. Significant bending of the penis can result in pain, poor
erections, and an inability to engage in sexual intercourse.

This disease affects about 3% of the male population. The average age of onset of this
disease is 57 years old. The cause of the disease is unknown. However, many believe that it
may be due to trauma to the penis (such as injury or extremely vigorous sexual activity).

Treatments for this disease have been limited and often unsuccessful. The goal of treatment
is to reduce pain and maintain sexual function. Oral medicines that prevent plaque formation
and promote plaque breakdown have not been effective. Many patients with the disease will
require injections of medicines directly into the plaque. These injections have been used
for over 50 years in the treatment of major Peyronie's disease. The disease often resolves
on its own without treatment. Surgery may be performed to remove hardened tissue in the
penis. However, surgery is not done during the first 12 months of the disease.

There are 2 phases of the disease: the active phase and the inactive phase. The active phase
usually occurs during the first 12 months of the disease. The stabilization of the plaque is
known as the inactive phase. We are inviting men with stable disease to take part in this
study which will test BOTOX® versus a placebo (a placebo contains no medicine).

This will be a randomized, placebo-controlled, cross-over, single-center trial. Study drug
is Botulinum toxin type A (BOTOX®). Subjects who meet the inclusion criteria for the study
will be randomized to either the treatment or placebo arm.

- Treatment: Injection solution will consist of 100 units of BOTOX® in 10 cc of
preservative free normal saline, or

- Placebo: Injection solution will consist of 10 cc preservative free normal saline.

Inclusion Criteria:

- Subjects with stable Peyronie's plaques.

- Males at least 18 years of age

- Must give informed consent.

Exclusion Criteria:

- Subjects in the active phase of Peyronie's disease.

- Subjects with less than 1 year history of Peyronie's disease.

- Subjects taking oral medications for Peyronie's disease which include Trentol,
Viagra, vitamin E, colchicines, L-arginine, and tamoxifen. There will be a 2 week
wash-out period if patients are on these medications.

- Subjects with more than 1 penile plaque will be excluded from the study.

- Subjects with calcified plaques demonstrated by ultrasound will be excluded from the
study.

- Known allergy or sensitivity to any components of the study medication (botulinum
toxin A), anesthetics, or any other product associated with the treatment and general
study procedures.

- Any medical condition or neuromuscular disorder that may put the patient at increased
risk with exposure to botulinum toxin A (BTX-A), including myasthenia gravis,
Eaton-Lambert syndrome, or amyotrophic lateral sclerosis.

- Patient taking aminoglycosides or any drug known to interfere with neuromuscular
transmission.

- Patient has hemophilia or other clotting factor deficiencies or disorders that cause
bleeding diathesis.

- Patient must not be taking aspirin, non-steroidal anti-inflammatory drugs, or
Coumadin for 7 or more days prior to Botox injection.

- Episode of unstable angina pectoris, myocardial infarction, transient ischemic
attack, or cerebrovascular accident within the past 6 months.
We found this trial at
1
site
1200 Moursund Street
Houston, Texas 77030
(713) 798-4951
Baylor College of Medicine Baylor College of Medicine in Houston, the only private medical school...
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mi
from
Houston, TX
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