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the effect of tibial nerve stimulation on urinary symptoms in multiple sclerosis

Effect of percutaneous posterior tibial nerve stimulation on treatment of lower urinary tract symptom in women patient multiple sclerosis who referred to Emam Khomeini hospital

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013031512820N1
Enrollment
20
Registered
2013-04-17
Start date
2013-04-04
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple sclerosis. Multiple sclerosis

Interventions

Patients will be treated with 12 sections of electrical posterior tibial stimulation. Each stimulation will be applied for 30 minutes, once a week for 12 weeks, by unilateral insertion of 38 monopolar
Treatment - Other

Sponsors

Vice-chancellor for research, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Women with Multiple Sclerosis (between 18-55 years old) who have lower urinary symptoms such as urgency, frequency and nacturia with detrusor sphincter dyssynergia or over active bladder refractory to drug therapy (treatment of at least three months with one or two anticholinergic drugs) are included in study. The exclusion criteria are: urinary infection; previous urogenital surgery; renal stone; pregnancy; severe cardiopulmonary diseases; physical inability; diabetes mellitus; other central nervous system diseases. Also, patients who don’t consent do not consider. When the urinary symptoms aggravate, attack of multiple sclerosis appear or weekly treatment are not followed, the patients are also removed from the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Maximum-systometric-capacity. Timepoint: Before and after intervention. Method of measurement: Urodynamic study.;Involuntary detrusor contraction volume. Timepoint: Before and after intervention. Method of measurement: Urodynamic study.

Secondary

MeasureTime frame
Frequency. Timepoint: In each refering. Method of measurement: Ask from the patients.;Nacturia. Timepoint: In each refering. Method of measurement: Ask from the patients.;PVR. Timepoint: Before and after of stimulation. Method of measurement: Nelaton Catheter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSarraf Payam

Tehran University of Medical Sciences

p-sarraf@tums.ac.ir+98 21 6119 2424

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026