Chemotherapy-Induced Peripheral Neuropathy - Additional Evaluation in Breast Cancer Survivors

ConditionBreast Cancer
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUniversity Hospital Schleswig-Holstein

About this trial

The main goal of this trial is to identify the optimal cut-off score of a Scoring System to discriminate between mild chemotherapy-induced peripheral neuropathy (CIPN) and no CIPN in breast cancer survivors previously treated with taxane-based chemotherapy and adjuvant radiotherapy.

Eligibility criteria

Qualifiers

Histologically proven breast cancer

Previous treatment with taxane-based chemotherapy followed by adjuvant radiotherapy

Mild or no CIPN according to the Total Neuropathy Score

Female gender

Disqualifiers

Disease-related skin disorders of the lower extremities (e.g., related to skin infections, bullous dermatoses, dermatitis, papulo-squamous skin disorders, or urticaria/erythema)

Pregnancy, Lactation

Expected non-compliance

Trial design

Treatments tested in this trial

  • Symptom-based scoring system

Treatment groups

28 Participants
are divided into 1 treatment group