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Clinical Trial Details — Status: Unknown status

Administrative data

NCT number NCT02452593
Other study ID # UFRGSDGO
Secondary ID
Status Unknown status
Phase N/A
First received April 8, 2015
Last updated May 21, 2015
Start date January 2014
Est. completion date August 2015

Study information

Verified date May 2015
Source Federal University of Rio Grande do Sul
Contact Magda Ms Aranchipe, Master
Email mchipe@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Urinary incontinence is defined according to the International Continence Society as any involuntary loss of urine, which may bring several negative consequences on women's lives, and among incontinent women, about 50% have urinary incontinence, 30% mixed and 20% emergency.

The overactive bladder present in urge incontinence and mixed cause significant impacts on people's lives and has a prevalence of 16.5% in the US population.

Behavioral therapies, exercises the pelvic muscles and drugs are the main forms of treatment. Drug therapy using drugs which are not specific for the bladder and are associated with many unwanted systemic side effects.

The results obtained by researchers in several countries using conservative techniques in the treatment of patients with urinary incontinence are encouraging and this study aims to evaluate carefully and systematically the effectiveness of tibial stimulation technique.

Importantly, also, that conservative techniques have lower cost than the surgical treatment and have virtually no side effects as most of the drugs used in the pharmacological treatment of female urinary incontinence.


Description:

Goal

Development of instrumentation for home treatment of overactive bladder and urgency / mixed incontinence using tibial stimulation and pelvic floor exercises.

Secondary objectives

- Development of an innovative portable equipment, with domestic technology for home application of the posterior tibial nerve stimulation technique using the type SSP surface electrodes (Silver Spike Point).

- Comparison of the effectiveness of tibial stimulation techniques and pelvic floor exercises in the treatment of overactive bladder and urgency / mixed incontinence.

Design Randomized Clinical Trial

Sample Women over the age of 18, complaining of urinary incontinence Urgency or Mixed (with main urgency component), catered in Urogynecology Ambulatory of Hospital de Clinicas de Porto Alegre.


Recruitment information / eligibility

Status Unknown status
Enrollment 30
Est. completion date August 2015
Est. primary completion date July 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Women with Urinary Incontinence of Urgency or Mixed older than 18 years

Exclusion Criteria:

- Presence Of vaginal or urinary infection

- Not understand or sign the informed consent

- Not understand or are unable to perform the proposed treatment

- Pregnancy or the postpartum period covering the period up to 6 months after delivery

- Women in previous use of chronically used drugs (antidepressants, diuretics, and others) that can evidently alter the urinary function.

- Stress Urinary Incontinence of pure or mixed incontinence with a predominance of Stress component neurogenic bladder

- Use of Botox® in the bladder or pelvic muscles in the last year

- Use Interstim® or Bion®

- Use pacemaker or implantable defibrillator

- Current use of TENS in the pelvic region, lower back or legs

- Previous use of percutaneous tibial stimulation

- Drug / experimental devices in the past 4 weeks,

- Participation in any clinical research involving or affecting the urinary or renal function in the last 4 weeks.

- Pelvic radiotherapy;

- Changes in sensibility Lower Limb;

Study Design


Intervention

Other:
"Tibial stimulation" and "pelvic floor exercises"
A group will make tibial nerve stimulation and the other will make pelvic floor training. After 8 weeks the patients exchanges their therapeutic approaches for over 8 weeks

Locations

Country Name City State
Brazil Hospital de Clinicas de Porto Alegre Porto Alegre Rio Grande do Sul

Sponsors (2)

Lead Sponsor Collaborator
Federal University of Rio Grande do Sul Hospital de Clinicas de Porto Alegre

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of participants with Urinary incontinence 3 months
See also
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Completed NCT04470765 - Transcutaneous Tibial Nerve Stimulation: the ZIDA Device Equivalence N/A
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Active, not recruiting NCT05241379 - AURA-2: Augmenting Urinary Reflex Activity N/A
Completed NCT02657057 - Effects of Transcutaneous and Percutaneous PTNS on Idiopathic OAB N/A
Withdrawn NCT00773552 - Solifenacin Succinate Versus Placebo in Inner City Women Ages 20-45 With Overactive Bladder Phase 4
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Completed NCT00337558 - A Study of Solifenacin With Bladder Training Versus Solifenacin Alone in Patients With Overactive Bladder (SOLAR) Phase 4
Completed NCT03180372 - Hybrid Fractional Laser Treatment for Symptoms of Urinary Incontinence N/A
Completed NCT05783219 - Lidocaine Patches Prior to Percutaneous Nerve Evaluation Phase 2
Active, not recruiting NCT05308979 - Intradetrusor Botulinum Toxin A for OAB Via 1 Versus 10 Injections: A Randomized Clinical Trial Phase 4
Completed NCT03672461 - A Group-Based Therapeutic Yoga Intervention for Urinary Incontinence in Ambulatory Older Women N/A
Completed NCT01391780 - Pelvic Floor Muscle Evaluation in Women With Stress Urinary and Urgency Urinary Incontinence N/A
Completed NCT03655054 - eCoin for OAB Feasibility Follow-on Study N/A