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NCT06724861

Sensory Rehabilitation in Chemo Induced Peripheral Neuropathy

Not yet recruiting NA Last updated 9 December 2024
What this trial tests

NA trial testing Explicit Sensory Retraining for the lower extremities in CIPN - Chemotherapy-Induced Peripheral Neuropathy in 27 participants. Not yet recruiting.

Timeline
11 December 2024
Primary endpoint
11 December 2024
11 December 2026

Quick facts

Lead sponsorAssaf-Harofeh Medical Center
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingdouble
Primary purposetreatment
Enrollment27
Start date11 December 2024
Primary completion11 December 2024
Estimated completion11 December 2026
Sites1 location across Israel

Drugs / interventions tested

Conditions studied

Sponsor

Assaf-Harofeh Medical Center

Who can join

18 and older, any sex, with CIPN - Chemotherapy-Induced Peripheral Neuropathy or Age Over 18. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is a cross-over RCT evaluating the effectiveness of 3 sessions a week apart of explicit sensory retraining to the lower extremities in individuals with CIPN versus usual care. The primary outcome measures are TNAS for subjective symptoms, VAS for pain and TUG for mobility. Additional outcome measures are FABS for balance, sensory assessments - monofilaments for touch threshold, LEPT for proprioception, a home exercise log and a satisfaction questionnaire.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for CIPN - Chemotherapy-Induced Peripheral Neuropathy

Currently open trials in the same condition.

Other Assaf-Harofeh Medical Center 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/NCT06724861.

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