• Bladder and TranscUtaneous Tibial Nerve Stimulation for nEurogenic Lower Urinary Tract Dysfunction

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ClinicalTrials.gov ID

NCT03965299

Lead Sponsor

University of ZurichOTHER

Overall Status

Recruiting

Study Type

Interventional

Phase

Not Applicable

Enrollment

114Estimated

Last Update Posted

Jan 20, 2026Actual

Start Date

Jun 19, 2019Actual

Primary Completion Date

Sep 30, 2026Estimated

Completion Date

Sep 30, 2026Estimated

Official Title

Transcutaneous Tibial Nerve Stimulation in Patients With Acute Spinal Cord Injury to Prevent Neurogenic Detrusor Overactivity: A Nationwide Randomised, Sham-controlled, Double-blind Clinical Trial

Brief Summary

Most patients with spinal cord injury (SCI) develop neurogenic lower urinary tract dysfunction (NLUTD), one of the most devastating sequelae of SCI which ultimately can lead to renal failure. We urgently need an intervention that prevents NLUTD before irreversible damage occurs. Neuromodulation procedures are a promising avenue so that we investigate the effect of transcutaneous tibial nerve stimulation (TTNS) in patients with acute SCI.

This nationwide randomized, sham-controlled, double-blind multicentre clinical trial includes all SCI centres in Switzerland (Basel, Nottwil, Sion, Zürich). Patients are randomly assigned to VERUM TTNS (active stimulation, n=57) and SHAM stimulation (n=57) groups in a 1:1 allocation using computer-generated permuted block randomisation lists stratified on study centre and lower extremity motor score. Daily 30-minute sessions are performed five times a week during an intervention period of 6-9 weeks. The primary outcome of this study is the success of TTNS to prevent neurogenic DO jeopardizing the upper urinary tract, assessed by urodynamics at 1 year after SCI or any earlier time point if DO treatment is necessary (study end). Secondary outcome measures are bladder diary parameters, clinical symptom scores assessed by standardized and validated questionnaires. Furthermore, neurophysiological and neuroimaging outcome measures are assessed as well as, biochemical and molecular changes. Tertiary outcome measure is the safety of TTNS.

Before the actual start of the TASCI RCT, start-up activities will include a piloting phase on groups of healthy volunteers and patients. The goal during this phase is to evaluate the feasibility of the experimental setup, in particular for the TTNS and SHAM intervention, but also to test the setup of the different pre and post assessments (e.g. neurophysiology and neuroimaging tests). Groups of up to 15 participants each will be enrolled in a few consecutive pilot studies allowing for fine tuning and small adaptations in between, if appropriate.

• Spinal Cord Injury, Acute

• VERUM TTNS
• SHAM TTNS

Ages Eligible for Study

Adult (18-64)Older Adult (65+)

Sexes Eligible for Study

All

Accepts Healthy Volunteers

No

Eligibility Criteria

Inclusion Criteria:

• Age >18 years

• Patients with acute SCI (traumatic SCI and sudden onset (<7 days) non-traumatic SCI) within 40 days after injury

• Patients with acute SCI at cervical or thoracic level

• Willing to take part and follow the requirements of the TASCI protocol (up to one year after SCI)

  • no percutaneous tibial nerve stimulation (PTNS)
  • no functional electrical stimulation (FES), apart from upper limb FES
  • no electrical muscle stimulation (EMS)

• Informed Consent

Exclusion Criteria:

• Contraindications to the investigational product
• DO with contractions greater than 40 cmH2O at a bladder filling volume of less than 500mL at baseline visit
• Treatment with antimuscarinics or with mirabegron
• Known or suspected non-adherence, drug or alcohol abuse
• Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant
• Participation in another study with investigational drug or product within the 30 days preceding and during the present study
• Neuromodulation treatment for urological or bowel indication in the last six months or ongoing
• Botulinum toxin injections in the detrusor and/or urethral sphincter in the last six months
• Bilaterally absent tibial nerve compound muscle action potential (cMAP, amplitude < 1mV)
• Women who are pregnant or breast feeding
• Intention to become pregnant during the course of the study
• Individuals especially in need of protection (according to Research with Human Subjects published by the Swiss Academy of Medical Sciences [www.samw.ch/en/News/News.html\])
• Enrolment of the investigator, his/her family members, employees and other dependent persons
• Pre-existing or concomitant medical condition apart from SCI that might pose a safety issue or would interfere with interpretation of study results or study conduct (e.g. Parkinson's disease, neurodegenerative disorders including multiple sclerosis and amyotrophic lateral sclerosis, urological malignancies)

Primary Purpose

Prevention

Allocation

Randomized

Interventional Model

Parallel Assignment

Masking

Triple

Lead Sponsor

University of ZurichOTHER

Collaborators

Swiss National Science FoundationOTHER

Clinique Romande de ReadaptationNETWORK

Rehab BaselOTHER

Swiss Paraplegic Research, NottwilNETWORK

BioMedical Research Forschungslabor für Urologie, University of BernUNKNOWN

Universidade do PortoOTHER

Center for Lower Urinary Tract Research School of Medicine, University of PittsburghUNKNOWN

s.moehr@rehab.ch