Comparison of the Effects of Transcutaneous Electrical Nerve Stimulation Protocols in Women With Overactive Bladder
NCT ID: NCT05672277
Last Updated: 2023-01-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
40 participants
INTERVENTIONAL
2023-02-15
2024-02-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Comparison of the Efficacy of Transcutaneos Nerve Stimulations in Women With Idiopathic Overactive Bladder
NCT06349694
Transcutaneous Tibial Nerve Stimulation for Urgency Urinary Incontinence
NCT04936464
Chronic Pelvic Pain Syndrome in Males
NCT06369545
Effect of Tibial Transcutaneous Electrostimulation in Women with Urgency Urinary Incontinence
NCT05590481
Home-Based Transcutaneous Remotely Monitored Posterior Tibial Neuromodulation
NCT07081412
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Group 1
Group 1 will be applied TENS three days per week
TENS 1
Parasacral TENS will be applied for 30 minutes 3 days a week during 6 weeks.
Group 2
Group 2 will be applied TENS one day per week
TENS 2
Parasacral TENS will be applied for 30 minutes one day a week during 6 weeks.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
TENS 1
Parasacral TENS will be applied for 30 minutes 3 days a week during 6 weeks.
TENS 2
Parasacral TENS will be applied for 30 minutes one day a week during 6 weeks.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Having diagnosed with OAB,
* Being a volunteer
Exclusion Criteria
* presence of severe pelvic organ prolapse,
* malignant disease,
* urinary infection,
* neurological disease,
* have electronic and metal implant,
* loss of sensation,
* lumbosacral peripheral nerve lesion
18 Years
65 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ankara Yildirim Beyazıt University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
seyda toprak celenay
associate professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Seyda Toprak Celenay
Role: PRINCIPAL_INVESTIGATOR
Ankara Yildirim Beyazıt University
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2023/01/02
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.