Surgical Glove Compression to Prevent Paclitaxel Neuropathy
Starting soon · Not applicable
Conditions studied: Paclitaxel-Induced Peripheral Neuropathy, Breast Cancer, Surgical Glove
In brief
This study aims to evaluate the effect of surgical glove compression as a prophylactic method to prevent paclitaxel-induced peripheral neuropathy. Participants will be randomly assigned to two groups: one receiving standard care, and the other receiving prophylactic surgical glove compression. The study will compare the development, severity of neuropathy in the hands and fingers, and its impact on quality of life.
Key facts
- Study ID
- NCT07504770
- Run by
- Necmettin Erbakan University
- People needed
- 84
- Starts
- 2026-03-26
- Expected to finish
- 2027-03-26
- Last updated by the study team
- 2026-04-17
Who can join
Age: 18 and older, up to 80. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Patients aged between 18 and 80 years
- Diagnosed with Stage II-III breast cancer
- No distant metastasis
- Planned to receive adjuvant or neoadjuvant paclitaxel for at least 12 weeks
- Willing and able to provide informed consent
- Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2 Karnofsky ≥ 60%)
You may not qualify if…
- Recurrent breast cancer
- Prior treatment associated with neuropathy (e.g., taxanes, platinum-based chemotherapy, anti-tubulin or proteasome inhibitors)
Where it is running
- Necmettin Erbakan University, Faculty of Health Sciences — Konya, Meram, Turkey (Türkiye)
Full record on ClinicalTrials.gov
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