EligibleTrials

The Efficacy of Compression/Ice Gloves/Socks in Patients With UTD1-induced Neuropathy.

Recruiting · NCT07638774 · Interventional (participants receive a specific treatment) · Lead sponsor: Fudan University

View the official record on ClinicalTrials.gov →
Breast cancer

Interventions studied

compression glove/sockice glove/sock

What this trial is about

This study is a prospective, multicenter, phase Ⅲ trial to evaluate of the compression/ice gloves/socks efficacy in UTD1-induced peripheral sensory and motor neuropathy. 324 patients will be included. All patients will be randomly divided into three groups at a ratio of 1:1:1. Group A is the blank control group, group B is the compression glove/sock group, and group C is the ice glove/sock group.

Who can take part

Age range
18 Years to 75 Years
Sex
Female
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)

Inclusion criteria

Exclusion criteria

Where it is running

1 location listed.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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