ClinicalTrials.Veeva

Menu

Compression Bandaging and Manual Lymph Drainage in Women With Lymphedema (LYMPHATIC)

U

University of Malaga

Status

Unknown

Conditions

Arm Lymphedema After Breast Cancer

Treatments

Other: Manual lymph drainage
Other: Multimodal treatment: compression bandaging and manual lymph drainage.

Study type

Interventional

Funder types

Other

Identifiers

NCT02165696
UMA_CBM_2014/LYMP
Lymphatic Multimodal Treatment

Details and patient eligibility

About

Lymphedema is the result of accumulation of fluid and other elements in tissue spaces because of an imbalance between the production of fluid interstitial and transport. Lymphedema can cause significant physical and psychological morbidity. Prevalence of lymphedema in patients after breast cancer surgery is 12-60% and the incidence is 12-26%.Psychological and social consequences of secondary lymphedema related breast cancer have been little recognized and documented. Although, it have performed many studies related secondary lymphedema it not found sufficient evidence in the literature to suggest the most effective treatment. There is some evidence suggesting that compression therapy and manual lymphatic drainage can improve lymphedema but more studies are needed. The aim of this research is to to evaluate the clinical effect of multimodal treatment (compression bandaging and manual lymph drainage) versus applying manual lymphatic drainage in women with arm lymphedema after breast cancer surgery.

Full description

This study has two sub research: a quantitative approach and a qualitative approach. The research will be carried out by a multicenter way

Quantitative approach consist in carried out a single-blind randomized controlled trial of 44 women with arm lymphedema. Patients will be distributed in two intervention groups by a randomized way. Participants will be given his assignment by closed envelope. Both treatments will be administered five days a week for six weeks. The experimental group (n=22) will receive multimodal treatment: combination of manual lymphatic drainage and compression bandaging. The control group (n=22) only will receive manual lymphatic drainage. We want to determinate the effect on volume arm decrease, quality of life, level of hand strength, degree of pain, fatigue level, and state of anxiety and depression. The influence on the lymphedema will be analyzed with lower limbs strength, physical activity, lung function, respiratory muscle strength by maximal inspiratory and expiratory pressure measurements (MIP and MEP) and cardiorespiratory functional capacity. Patients adherence will be analyzed by a smartphone.

Qualitative apprach: to know the perceptions and experiences of the participants in both interventions groups through a qualitative descriptive study. Data will be obtained with semi-structured depth interview.

Enrollment

44 estimated patients

Sex

Female

Ages

45 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Women between 45 and 65 years with secondary lymphedema in upper limb after breast cancer surgery.
  • Cancer stages I-III according to TNM classification of the American Joint Committee on Cancer.

Exclusion criteria

  • To have received lymphedema treatment previously.
  • To be treated by radiation therapy or chemotherapy.
  • Distant metastases or local recurrence of cancer.
  • Infectious signs in the upper limb with lymphedema.
  • Uncontrolled hypertension.
  • Heart disease.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

44 participants in 2 patient groups

Manual lymphatic drainage and compression bandaging
Experimental group
Description:
Experimental group: 30 minutes and one hour maximum time of manual lymphatic drainage and compression bandaging with multilayer inelastic bandages with low extensibility. It is possible to apply bandages two or three times per week. Also, an elastic bandage is also held in hand fingers with slight compression and other protective bandage is used in skin. The treatment will be carried out for six weeks five days a week
Treatment:
Other: Multimodal treatment: compression bandaging and manual lymph drainage.
Manual lymphatic drainage
Active Comparator group
Description:
Control group: 30 minutes and one hour maximum time of manual lymphatic drainage. The treatment will be carried out for six weeks five days a week.
Treatment:
Other: Manual lymph drainage

Trial contacts and locations

1

Loading...

Central trial contact

Martín-Valero R., Ph D

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems