Your session is about to expire
← Back to Search
Antibiotics for Overactive Bladder Post-Botox
Phase 4
Recruiting
Research Sponsored by University of Alberta
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1, 2 and 6 weeks following the procedure
Awards & highlights
All Individual Drugs Already Approved
Approved for 40 Other Conditions
Pivotal Trial
Drug Has Already Been Approved
Summary
This trial is testing if taking antibiotics right after Botox injections in the bladder can prevent infections in women with overactive bladder. The goal is to see if antibiotics reduce the risk of bladder infections after the procedure. Botox A was approved by the U.S. Food and Drug Administration for the treatment of overactive bladder.
Who is the study for?
This trial is for women over 18 with an overactive bladder (OAB) that hasn't improved with medication. It's not for those under 18, pregnant or breastfeeding, men, anyone allergic to Botox or Ciprofloxacin, currently have a UTI or can't empty their bladder fully.
What is being tested?
The study tests if taking the antibiotic Ciprofloxacin after getting Botox injections in the bladder reduces infections compared to a placebo pill. Women are randomly assigned to one of these two groups and followed up for six weeks.
What are the potential side effects?
Possible side effects include reactions related to antibiotics like stomach upset, rash, and yeast infections. There may also be typical Botox injection issues such as pain at the injection site or difficulty urinating.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1, 2 and 6 weeks following the procedure
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1, 2 and 6 weeks following the procedure
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Rate of Postoperative Urinary Tract Infection
Secondary study objectives
Rate of Other Adverse Events
Rate of Postoperative Urinary Tract Infection Rate
Awards & Highlights
All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
Approved for 40 Other Conditions
This treatment demonstrated efficacy for 40 other conditions.
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Drug Has Already Been Approved
The FDA has already approved this drug, and is just seeking more data.
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: Treatment ArmActive Control1 Intervention
Ciprofloxacin 500 mg PO every 12 hrs for 3 days following the procedure
Group II: Placebo ArmPlacebo Group1 Intervention
Placebo pill PO every 12 hrs for 3 days following the procedure
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for Overactive Bladder (OAB) include anticholinergics and beta-3 adrenergic agonists. Anticholinergics work by blocking acetylcholine receptors in the bladder, which reduces involuntary contractions and helps increase bladder capacity.
Beta-3 adrenergic agonists relax the bladder muscle by stimulating beta-3 receptors, also increasing bladder capacity and reducing urgency and frequency of urination. These treatments are crucial for OAB patients as they directly address the symptoms of urgency, frequency, and incontinence, significantly improving quality of life.
Find a Location
Who is running the clinical trial?
University of AlbertaLead Sponsor
937 Previous Clinical Trials
433,622 Total Patients Enrolled
Women and Children's Health Research Institute, CanadaOTHER
17 Previous Clinical Trials
24,698 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am female.I am male.I am not allergic to Botox, do not have a UTI, can empty my bladder fully, and am willing to follow post-treatment instructions.I am on antibiotics and understand the risks with Botox injections.I have overactive bladder due to a neurological condition like MS or spinal cord injury.I am under 18 years old.I am allergic to Ciprofloxacin or similar drugs, or I am taking Tizanidine or Agomelatine.I am 18 years old or older.I have OAB not caused by any known condition and treatments haven't worked.
Research Study Groups:
This trial has the following groups:- Group 1: Treatment Arm
- Group 2: Placebo Arm
Awards:
This trial has 4 awards, including:- All Individual Drugs Already Approved - Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
- Approved for 40 Other Conditions - This treatment demonstrated efficacy for 40 other conditions.
- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
- Drug Has Already Been Approved - The FDA has already approved this drug, and is just seeking more data.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Share this study with friends
Copy Link
Messenger