Alfuzosin for Voiding Dysfunction in Multiple Sclerosis (MS)
A Pilot Study Looking At The Use Of Alfuzosin In The Treatment Of Bladder Dysfunction In Patients With Multiple Sclerosis
What it found
The trial ended early for another reason (see below).
Reason given: Lack of funding
This trial finished 17 years ago. We found no results in the registry or in any paper that cites it.
What was tested
Treatment tested
- Alfuzosin
What it measured
Main measures
The primary efficacy measures will be the ICIQ-LUTSqol questionnaire, the IPSS questionnaire, uroflow/PVR and the voiding diaries.
12 weeks
Bladder, bowel and sexual function
Who could take part
MS (type not specified) · 18 and over
Show the full criteria
Inclusion criteria
1. Participant should be eighteen years of age or older. 2. Participant should have LUTS secondary to Multiple Sclerosis as defined below. 3. Participant should have frequency ≥ 8/day and/or incontinence and/or nocturia ≥ 2/night and/or urgency and/or urinary retention. 4. Participant should be able to understand, speak and read English. 5. Participant 's urine culture should not show any evidence of urinary tract infection. 6. Participant should be willing to take part in the study and sign the consent form. 7. Female participants consents to use a medically acceptable method of birth control throughout the entire study period and for four weeks after the study is completed. Medically acceptable methods of contraception that may be used by the study participants and/or their partner includes abstinence, birth control pills or patches, diaphragm with spermicide, IUD, condom and vaginal spermicide, surgical sterilization, vasectomy, progestin implants or injections.
Exclusion criteria
1. Participant with known hypersensitivity to Alfuzosin. 2. Participant with history of postural hypotension and/or syncope. 3. Participant has used another alpha blocker within the last 30 days. 4. Participant has active urethral stricture disease. 5. Participant has a history of prostate cancer within the preceding five years. 6. Participant has hepatic dysfunction. 7. Participant has renal dysfunction. 8. Participant has unstable angina pectoris. 9. Participant has a positive pregnancy test at the time of screening. 10. Participant has a history of serious social, mental or medical conditions that would stop patient from taking part in the study. 11. Participant has a history of alcohol or drug abuse within the last five years. 12. Participant who is currently being treated for chronic bacterial prostatitis or painful bladder syndrome/interstitial cystitis. 13. Participant has a significant medical problem which the investigator considers a serious risk for the patient to be part of the study. 14. Use of any investigational drug or device within the last 6 months. 15. Participant who is unwilling or unable to abide by the requirements of study. 16. Participant has a bladder infection proven by urine culture.
As registered. Criteria can change, so ask the trial team or your neurologist.
About this trial
In the sponsor's words
Multiple Sclerosis is often associated with severe functional deficits resulting in a range of progressive impairments. Approximately 80% of patients have bladder symptoms at the time of diagnosis and up to 97% will have bladder symptoms during the course of the disease. To date, the vast majority of treatment has been centered on the use of medications to control "bladder spasms" and the use of catheters to help patients empty the bladder. There have been very few studies looking at medications like Alfuzosin that may help in controlling bladder symptoms in Multiple Sclerosis. Alfuzosin has been shown to significantly improve voiding symptoms and bladder emptying in patients with prostatic enlargement. There have been no controlled studies yet to determine whether this treatment helps patients with Multiple Sclerosis. The purpose of this study is to determine if Alfuzosin improves bladder symptoms and quality of life in patients with Multiple Sclerosis.
Loading reviews and guidelines…
History
Started
Nov 2007
Main results due
Nov 2009
Finished
Nov 2009