Using cohesive bandages to treat axillary web syndrome after breast cancer surgery
Effectiveness of Cohesive Bandage on Axillary Web Syndrome After Breast Cancer Surgery: a Randomized Controlled Trial
This study is testing if using special bandages along with exercises can help women with axillary web syndrome feel better after breast cancer surgery compared to regular physical therapy.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 90 (estimated) |
| Ages | 18 Years to 70 Years |
| Sex | Female |
| Sponsor | University of Alcala Academic / other |
| Locations | 1 site (Alcalá De Henares, Madrid) |
| Trial ID | NCT04338334 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the effectiveness of cohesive bandages in treating axillary web syndrome, a condition that can occur after breast cancer surgery. The study involves a randomized single-blinded controlled design with 90 women who have undergone unilateral breast cancer surgery. Participants will be divided into two groups: one receiving cohesive bandaging along with therapeutic exercises, and the other receiving standard physical therapy. Follow-up assessments will be conducted at multiple intervals to measure pain, swelling, and shoulder mobility.
Who should consider this trial
Good fit: Ideal candidates are women who have undergone unilateral breast cancer surgery and are experiencing axillary web syndrome.
Not a fit: Patients with cognitive or visual impairments, bilateral breast cancer, or other systemic diseases may not benefit from this study.
Why it matters
Potential benefit: If successful, this treatment could significantly improve pain management and functional recovery for patients with axillary web syndrome.
How similar studies have performed: While similar approaches have been explored, this specific intervention using cohesive bandages is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Unilateral breast cancer; * Breast surgery with lymphadenectomy and / or sentinel lymph node biopsy; * Axillary web syndrome in upper limb of the operated side; * Consent to participate in the study; * No contraindications. Exclusion Criteria: * Cognitive impairment; * Visual impairment for reading; * Lymphedema; * Bilateral breast cancer; * Systemic disease (metastases), * Infection; * Locoregional recurrence.
Where this trial is running
Alcalá De Henares, Madrid
- María Torres-Lacomba — Alcalá De Henares, Madrid, Spain (Recruiting)
Study contacts
- Principal investigator: María Torres-Lacomba, PhD — University of Alcalá
- Study coordinator: María Torres-Lacomba, PhD
- Email: maria.torres@uah.es
- Phone: +34678900061
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.