CompletedNot Applicable

Effect of Different Bandage Interface Pressures on Breast Cancer Related Lymphedema

Turkey (Türkiye)21 participantsStarted 2019-06-01

Plain-language summary

The goal of this randomised comparison study is to compare different bandage interface pressures in individuals with breast cancer related lymphedema The main questions it aims to answer are: * Is high or low bandage pressure effective in reducing edema and soft tissue thickness? * do bandages applied with high or low bandage pressure comprimise sleep, comfort or subjective benefit from treatment? Participants will recieve complex decongestive physiotherapy. Bandage will apply high or low pressure. Effects of high and low bandage interface pressures will compare

Who can participate

Age range

18 Years – 85 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Stage 2 unilateral BCRL involving whole extremity according to ISL * To be volunteer. Exclusion Criteria: * Acute deep vein thrombosis * Acute soft tissue infection * Peripheral artery disease in upper extremity * Systemic diseases with peripheral edema (kidney, hearth insufficiency etc.), * Allergy to materials used for treatment * Mental diseases effect cooperation * Sensory loss in the effected limb * Open wound in the effected limb.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

change from baseline skin and subcutanetous thickness with 4 weeks treatment and follow up

Timeframe: baseline, 1.day, 2 weeks, 4 weeks, 3 months (follow-up)

change from baseline residual volume with 4 weeks treatment and follow up

Timeframe: baseline, 1.day, 2 weeks, 4 weeks, 3 months (follow-up)

Trial details

NCT IDNCT05660590

SponsorAbant Izzet Baysal University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-04-22

View on ClinicalTrials.gov More Lymphedema of Upper Limb trials