Comparison of Electroacupuncture to Mirabegron for Treatment of Overactive Bladder
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Details and patient eligibility
About
This study compares electroacupuncture to mirabegron for treatment of overactive bladder (OAB) symptoms in women who have failed treatment with anticholingeric therapy.
Full description
Screening/Eligibility Visit:
If it is determined that a patient with a diagnosis of OAB has failed therapy with at least one anti-cholinergic agent, the potential participant will be screened and eligibility will be confirmed by a study investigator. A signed, IRB-approved informed consent will be obtained.
Randomization:
Randomization will be performed after the patient has agreed to participate and discussed and signed the informed consent form. Patients will be randomized in random blocks of 4, 6 and 8 into either the acupuncture group or mirabegron group. Once patient participation is confirmed, an enveloped marked with the study participant number will be opened by one of the study investigators in front of the patient.
Acupuncture Protocol:
All acupuncture sessions will be performed by a licensed acupuncturist employed by University Hospitals Connor Integrative Health Network. All acupuncturists involved in the study protocol will be trained and supervised in the correct technique by Christine Kaiser, MS, LAc, Dipl.OM. Acupuncture session will be performed weekly for 6 weeks and will be scheduled to accommodate both the patient's and acupuncturists' schedules. Acupuncture sessions will last for 30 minutes. Selected points will include kidney 3, kidney 6, spleen 6, and ren 4. The current delivery with electroacupuncture is approximately 10-20 mA (adjusted to patient sensation) delivery at 10 Hz for 30 minutes per session. After completion of 6 weeks of treatments patients will be contacted by phone at 2 week intervals to determine duration of symptomatic relief after cessation of treatment..
Mirabegron Protocol:
Patients assigned to the medication group will be prescribed 50 mg of myrbetriq daily to take for 6 weeks. At the completion of the study, if patients are satisfied with the effect of mirabegron they may continue to use it at their discretion.
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Ages
Volunteers
Inclusion criteria
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- Patients must be 18 years or older as well as willing and able to provide informed consent
- Patients with documented symptoms of overactive bladder including: urgency, frequency >7 times per day, nocturia, urgency incontinence for at least 6 months
- Patients who have failed at least one anti-cholinergic medication defined as no change or unsatisfactory improvement in symptom severity after 6 weeks of a daily regimen
Exclusion criteria
- Patients younger than 18 years,
- Patients unable or unwilling to provide informed consent,
- Patients who are illiterate,
- Patients who are non-English speaking or reading,
- Patients with a current urinary tract infection
- Patients with a history of interstitial cystitis
- Patients who have a history of a bleeding disorder
- Patients who are currently on chronic anti-coagulation
- Patients who are have taken mirabegron in the past or are currently using it
- Patients currently undergoing acupuncture treatment for a different condition
- Patients who are currently undergoing pelvic floor physical therapy
- Patients who are currently undergoing or will undergo treatment for a urologic or gynecologic malignancy
- Patients who are currently pregnant
- Patients with an implanted pacemaker or AICD
- Patients with a history of uncontrolled or poorly controlled hypertension
Trial design
Primary purpose
Allocation
Interventional model
Masking
0 participants in 2 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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