Actively Recruiting
Subclinical Monitoring of Lymphatic Function in Oncology Patients for Lymphoedema Prevention (ONCOLYMPH)
Led by The Greater Poland Cancer Centre · Updated on 2025-06-08
600
Participants Needed
1
Research Sites
260 weeks
Total Duration
On this page
Sponsors
T
The Greater Poland Cancer Centre
Lead Sponsor
P
Poznan University of Physical Education
Collaborating Sponsor
AI-Summary
What this Trial Is About
Lymphoedema, a chronic condition caused by the accumulation of protein-rich fluid in the intercellular spaces due to impaired lymphatic function, is a common complication in cancer patients. It can lead to visible swelling, discomfort, and mobility issues, but most frequently affects the limbs. This condition not only impacts patients physically but also has significant psychological consequences, including reduced quality of life, social stigma, and challenges with returning to daily activities. Oncology patients are particularly at risk for developing lymphoedema due to factors such as lymphadenectomy, radiotherapy, and extensive surgical procedures. Up to 30% of breast cancer survivors develop lymphoedema, and it is also a common complication in patients treated for other cancers, such as those involving the cervix, vulva, prostate, and bladder. Despite the importance of early detection, diagnostic tools for assessing lymphatic dysfunction are often specialised and not suitable for routine screening in clinical practice. The primary goal of this study is to explore the early signs of lymphatic dysfunction in cancer patients before evident clinical symptoms, with the aim of identifying individuals at risk of developing lymphoedema. This will provide valuable information that could guide early interventions and preventive measures to reduce the severity or even prevent the onset of lymphoedema. By focusing on early, subclinical dysfunction, the study seeks to contribute to improving both the clinical management of lymphatic complications and the overall quality of life for oncology patients. Regular monitoring and timely physiotherapy interventions could play a key role in enhancing recovery outcomes and reducing the long-term impact of lymphoedema.
CONDITIONS
Official Title
Subclinical Monitoring of Lymphatic Function in Oncology Patients for Lymphoedema Prevention (ONCOLYMPH)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Admission to the Greater Poland Cancer Centre for treatment in participating departments
- Age 18 years or older
- Ability to stand independently for 30 seconds
- Written informed consent to participate in the study
You will not qualify if you...
- Age 18 years or younger
- Cardiac arrhythmia
- Presence of pacemakers or other implanted electronic devices
- History of external defibrillation
- Pregnancy
- Critical limb ischaemia
- Advanced heart failure (NYHA III and IV)
- Symptoms of deep vein thrombosis
- Uncompensated heart, kidney, or thyroid failure
- Peripheral nerve damage
- Psychiatric disorders that prevent informed consent or limit cooperation
- Lack of informed consent to participate
AI-Screening
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Trial Site Locations
Total: 1 location
1
The Greater Poland Cancer Centre
Poznan, Greater Poland Voivodeship, Poland, 61-866
Actively Recruiting
Research Team
E
Ewa Tańska, PhD
CONTACT
J
Janusz Doś, PT, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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