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NCT03616353: IMPACTS

IMpact of Perineural Hydrodissection Over Alternative Therapies in Patients With Carpal Tunnel Syndrome

Status unknown EARLY_PHASE1 Last updated 9 August 2019
What this trial tests

EARLY_PHASE1 trial testing Perineural Hydrodissection in Carpal Tunnel Syndrome in 60 participants. Status unknown.

Timeline
15 October 2018
Primary endpoint
30 June 2020
30 June 2020

Quick facts

Lead sponsorLeslie Witton
PhaseEARLY_PHASE1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designsingle group
Maskingtriple
Primary purposetreatment
Enrollment60
Start date15 October 2018
Primary completion30 June 2020
Estimated completion30 June 2020
Sites1 location across Canada

Drugs / interventions tested

Conditions studied

Sponsor

Leslie Witton

Who can join

18 and older, any sex, with Carpal Tunnel Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a multidisciplinary, single-blinded, three-arm randomized controlled trial, comparing perineural hydrodissection and steroid injection for the treatment of CTS. Patients are screened based on pre-established eligibility criteria and randomized to one of the three study groups. Patients are followed at 6-week, 3-month, 6-month, and 12-month time points to assess the primary and secondary outcomes of the study, which include both patient-reported outcome measures and objective clinical assessments.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Carpal Tunnel Syndrome

Currently open trials in the same condition.

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Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing