Botox for Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS)

NCT ID: NCT00529386

Last Updated: 2019-03-25

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1
• Total Enrollment: 7 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-01-31
• Study Completion Date: 2009-12-31

Brief Summary

The objective of this study is to evaluate the safety and efficacy of intraprostatic injection of Botox for the treatment of men diagnosed with chronic nonbacterial prostatitis/chronic pelvic pain syndrome (CP/CPPS).

Detailed Description

This is a prospective open label study examining the efficacy and safety of intraprostatic Botox . Men with a clinical diagnosis of chronic nonbacterial prostatitis/CPPS will be treated with intraprostatic Botox™ and followed for 12 weeks (primary efficacy analyses), and 24 weeks (long term follow-up) for responders.

It is proposed that a total of 40 males will be enrolled. There will be seven (7) research clinic visits and two phone contacts: Visit 1 (screening), Visit 2 (baseline/treatment), Visit 3 (2-week safety evaluation - clinic contact), Visit 4 (4-week safety evaluation - phone contact), Visit 5 (6-week interim efficacy/safety), Visit 6 (12-week primary endpoint evaluation), Visit 7 (14-week clinic follow up), Visit 8 (16 week phone contact) and Visit 9 (24-week clinic close out).

Outcome measures include Chronic Prostatitis Symptom Index (CPSI 0-35), NRS pain (0-10), Global Response Assessment (GRA) at 12 weeks. Safety to be monitored during the study.

Conditions

Prostatitis; Chronic Pain Syndrome

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Botox

300 IU botox

Group Type: EXPERIMENTAL

Botox

Intervention Type: DRUG

300 units

Interventions

Botox

300 units

Intervention Type: DRUG

Other Intervention Names

Botulinem toxin

Eligibility Criteria

Inclusion Criteria

1. Participant has signed and dated the appropriate Informed Consent document.

2. Participant must be ≥ 18 years of age.

3. Participant has had a clinical diagnosis of chronic nonbacterial prostatitis (chronic pelvic pain syndrome) (CPPS) defined as symptoms of discomfort or pain in the perineal or pelvic region for at least the past 3 months without evidence of bacterial infection.

4. Participants must report ejaculatory pain and/or perineal discomfort.

5. Participants must have pain or discomfort localized to perineum or prostate during physical examination.

6. Participants must have an aggregate score of greater than or equal to 15 on the National Institutes of Health chronic prostatitis symptom index (NIH-CPSI).

7. Participant must have > 8 on the pain domain sub-score of the NIH-CPSI.

8. Participant must have had empiric treatment with 4 weeks fluoroquinolone, and subsequently failed the antibiotic therapy.

Exclusion Criteria

1. Participant has a history of prostate, bladder or urethral cancer.

2. Participant has inflammatory bowel disease (such as Crohn's disease or ulcerative colitis, but not irritable bowel syndrome).

3. Participant has undergone pelvic radiation or systemic chemotherapy.

4. Participant has undergone intravesical chemotherapy.

5. Participant has been treated for unilateral orchialgia without pelvic symptoms.

6. Participant has a current urethral stricture and/or bladder stones.

7. Participant has a neurological disease or disorder affecting the bladder.

8. Participant has a neurological impairment or psychiatric disorder preventing his understanding of consent and his ability to comply with the protocol.

9. Participant has a documented UTI within the last 3 months.

10. Participant has evidence of facultative Gram negative or enterococcus with a value of ≥ 1000 CFU/ml in mid-stream urine (VB2).

11. Participant has had previous intraprostatic injection of Botox.

12. Participant currently enrolled in an investigational study.

13. Participant interested in future fertility/fathering children.

14. Participant with urinary retention (PVR >200cc).

15. Participant having had prostate surgery in the past 3 months.

16. Participant having had minimally invasive surgical therapy for BPH.

17. Participant with a cystostomy or nephrostomy.

18. Participant with penile or urinary sphincter implants.

19. Participant with previous rectal surgery, current rectal disease or peri-rectal inflammatory disorders except hemorrhoidectomy.

20. Participant with PSA >10 ng/ml(PSA range 4-10, biopsy at PI discretion (deferral).

• Minimum Eligible Age: 18 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

Allergan

INDUSTRY

Sponsor Role: collaborator

Queen's University

OTHER

Sponsor Role: lead

Responsible Party

Dr. J. Curtis Nickel

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

J. Curtis Nickel, MD FRCSC

Role: PRINCIPAL_INVESTIGATOR

Queen's University

Locations

Centre for Advanced Urological Research

Kingston, Ontario, Canada

Countries

Canada

Other Identifiers

BOTOX-CP

Identifier Type: -

Identifier Source: org_study_id