- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06220903
The Effect of Complex Decongestive Therapy in Patients With Lymphedema
The Effect of Complex Decongestive Therapy on Fluid Excretion From The Body in Patients With Lymphedema
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The lymphatic system is the accessory circulatory system that takes lymph fluid from the interstitial space and adds it to the blood circulation. It starts from the interstitial space. It consists of lymph vessels, lymph fluid and lymphatic organs. Lymph fluid passes through many lymph nodes during its transport and is filtered in these nodules. The lymphatic system takes lymphatic fluid from the tissues and brings it to the venous part of the circulatory system. The main task of the lymph system is to reabsorb substances that cannot be absorbed by the blood circulation system. Non-absorbable substances in the interstitial space are called lymphatic load. Lymphatic load; It consists of protein, water, fat and cells. The aim of lymphedema treatment is to remove the protein-rich fluid accumulated in the interstitial space into the venous system. There are many factors in the flow of lymph fluid into the veins. The most important of these is the high filtration pressure that occurs when fluid is filtered through blood capillaries. Lymph fluid flowing from the periphery to the center is generally affected by pressure changes and moves from where the pressure is high to where it is low. Contraction of the muscles adjacent to the lymph vessels, pulsation of the neighboring arteries, and the effect of the smooth muscles in the lymph vessel wall also cause pressure changes. Other factors include respiratory movements acting as a pump in the lymph flow, the actual pressure effect of abdominal pressure on the cisterna chyli, and negative intrathoracic pressure.
Complex Decongestive Physiotherapy is proven effective and considered the gold standard for the treatment of lymphedema. It increases the hydrostatic pressure that has decreased due to edema and helps the lymph fluid to re-enter the circulation.
Purpose of the study; To objectively investigate whether the lymph fluid added to the circulation through Complex Decongestive Physiotherapy in lymphedema patients has an effect on fluid excretion from the body.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Beykoz
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Istanbul, Beykoz, Turkey, 34100
- Istanbul Medipol University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Female cases
- Cases diagnosed with lower extremity unilateral/bilateral lymphedema
- Having received or not received radiotherapy and/or chemotherapy
Exclusion Criteria:
- Having received treatment for lymphedema in the last year
- Having metastatic disease
- Those diagnosed with severe heart failure and/or arrhythmia
- Arterial disorders
- Kidney diseases
- Infection in affected extremities
- Psychological disorders
- Diabetes
- Nephrotic syndrome
- Diuretic use
- Patients using chemotherapy and drugs that have toxic effects on the kidneys
- Those with liver cirrhosis, liver disease
- Neurological diseases
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Treatment Group
Complex DecongestivePhysiotherapy program was planned for the affected extremity of the cases.
The treatment was performed 5 days a week, for 4 weeks, for a total of 20 sessions and each session was 60 minutes.
The treatment included Manual Lymph Drainage, skin care, multi-layer bandaging, exercise and compression stockings.
|
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
MoistureMeterD Compact Device
Time Frame: 4 weeks
|
Tissue dielectric constant technique provides information about the emergence of lymphedema in the early stages and the change in the amount of water under the skin.
A high-frequency electromagnetic wave produced by the device is directed to the skin by contacting the probe with the skin.
The effective measurement depth is 2.5 mm.
The device evaluates the amount of water under the tissue thought to be the beginning of lymphedema.
|
4 weeks
|
|
Liquid Intake-Urine Excretion Tracking
Time Frame: 4 weeks
|
The subjects were asked to fill out a 24-hour fluid intake-urine excretion chart to evaluate the difference between fluid intake and urine excretion.
|
4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Body Mass Index
Time Frame: 4 weeks
|
BMI values of the cases; Calculated and recorded using TANITA MC 780 S Professional Body Analysis Monitor.
It was calculated with the formula Body Mass Index (BMI) = Weight/Height2 (kg/m2).
|
4 weeks
|
|
Range of motion
Time Frame: 4 weeks
|
Universal Goniometer was used to evaluate joint range of motion.
Hip, knee and foot flexion were measured.
|
4 weeks
|
|
Evaluation of edema
Time Frame: 4 weeks
|
While the patients were in a semi-sitting position and the foot and ankle were in neutral position, circumference measurements were made with a tape measure at 5 cm intervals from the ankle to the lateral malleolus level towards the proximal.
Extremity volume was determined by calculating with the frustum formula.
The difference between both extremities (healthy and diseased side) was determined and measurements were made every day before and during treatment.
|
4 weeks
|
|
Lymphedema Quality of Life
Time Frame: 4 weeks
|
The patients' quality of life was evaluated using the Lymphedema Quality of Life Questionnaire-Lower extremity, which consists of questions about symptoms, body image, function and mode, respectively.
|
4 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Cemile Uydur, MsC, Avrupa Şafak Hospital Physical Therapy and Rehabilitation Unit
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MedipolU-FTR-DO-02
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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