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NCT03671993

Clinical Effect Observation for Electrical Pudendal Nerve Stimulation in Treating Urethral Pain Syndrome

Completed NA Last updated 3 December 2019
What this trial tests

NA trial testing Electrical pudendal nerve stimulation in Pelvic Pain Syndrome in 50 participants. Completed in 10 March 2019.

Timeline
5 October 2018
Primary endpoint
10 February 2019
10 March 2019

Quick facts

Lead sponsorShanghai Institute of Acupuncture, Moxibustion and Meridian
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment50
Start date5 October 2018
Primary completion10 February 2019
Estimated completion10 March 2019
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Shanghai Institute of Acupuncture, Moxibustion and Meridian

Who can join

Adults 18 to 75, any sex, with Pelvic Pain Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In this randomized controlled trial, we intend to determine whether electrical pudendal nerve stimulation is more effective than intravesical instillation in urethral pain syndrome.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. The short-term efficacy of electrical pudendal nerve stimulation versus intravesical instillation for the urethral pain syndrome: a randomized clinical trial.
    Li T, Feng XY, Feng XM, Lv JW, et al · · 2021 · cited 3× · PMID 33934208 · DOI 10.1007/s00345-021-03698-2

Verify or expand the search:

Other trials of Electrical pudendal nerve stimulation

Trials testing the same drug.

Other recruiting trials for Pelvic Pain Syndrome

Currently open trials in the same condition.

Other Shanghai Institute of Acupuncture, Moxibustion and Meridian trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03671993.

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