bTUNED: transcutaneous tibial nerve stimulation for neurogenic lower urinary tract dysfunction

Author:

Stalder Stephanie A.1ORCID,Gross Oliver1ORCID,Anderson Collene E.12ORCID,Bachmann Lucas M.3ORCID,Baumann Sarah1,Birkhäuser Veronika1ORCID,Bywater Mirjam4,del Popolo Giulio5ORCID,Engeler Daniel S.6ORCID,Agrò Enrico Finazzi7ORCID,Friedl Susanne8ORCID,Grilo Nuno9ORCID,Kiss Stephan4,Koschorke Miriam1ORCID,Leitner Lorenz1ORCID,Liechti Martina D.1ORCID,Mehnert Ulrich1ORCID,Musco Stefania5ORCID,Sadri Helen1,Stächele Lara1ORCID,Tornic Jure10ORCID,van der Lely Stéphanie1ORCID,Wyler Stephen4,Kessler Thomas M.1ORCID

Affiliation:

1. Department of Neuro‐Urology, Balgrist University Hospital University of Zürich Zürich Switzerland

2. Swiss Paraplegic Research, Nottwil and Department of Health Sciences and Medicine University of Lucerne Lucerne Switzerland

3. Medignition Inc. Research Consultants Zürich Switzerland

4. Department of Urology Cantonal Hospital Aarau Aarau Switzerland

5. Department of Neuro‐Urology Azienda Ospedaliera‐Universitaria Careggi Florence Italy

6. Department of Urology, School of Medicine University of St. Gallen St. Gallen Switzerland

7. Unit of Urology, Department of Surgical Sciences, Tor Vergata University Hospital Tor Vergata University Rome Italy

8. Spinal Cord Injury Center, Balgrist University Hospital University of Zürich Zürich Switzerland

9. Department of Urology Lausanne University Hospital Lausanne Switzerland

10. Department of Urology Cantonal Hospital Winterthur Winterthur Switzerland

Abstract

ObjectiveTo present the protocol for a randomized controlled trial (RCT) evaluating the efficacy and safety of transcutaneous tibial nerve stimulation (TTNS) for refractory neurogenic lower urinary tract dysfunction (NLUTD).Study Design and ResultsbTUNED (bladder and TranscUtaneous tibial Nerve stimulation for nEurogenic lower urinary tract Dysfunction) is an international multicentre, sham‐controlled, double‐blind RCT investigating the efficacy and safety of TTNS. The primary outcome is success of TTNS, defined as improvements in key bladder diary variables at study end compared to baseline values. The focus of the treatment is defined by the Self‐Assessment Goal Achievement (SAGA) questionnaire. Secondary outcomes are the effect of TTNS on urodynamic, neurophysiological, and bowel function outcome measures, as well as the safety of TTNS.ConclusionsA total of 240 patients with refractory NLUTD will be included and randomized 1:1 into the verum or sham TTNS group from March 2020 until August 2026. TTNS will be performed twice a week for 30 min during 6 weeks. The patients will attend baseline assessments, 12 treatment visits and follow‐up assessments at the study end.

Funder

Swiss Continence Foundation

Publisher

Wiley

Subject

Urology

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