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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02369679
Other study ID # 2014/5584/I
Secondary ID
Status Completed
Phase N/A
First received February 4, 2015
Last updated April 5, 2017
Start date October 13, 2014
Est. completion date April 5, 2017

Study information

Verified date April 2017
Source Parc de Salut Mar
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Treatment of lymphedema is based on a combined program called complex decongestive therapy. The components of the complex decongestive therapy are skin care, kinesiotherapy, manual lymphatic drainage and compression. The compression with multilayer bandage has proved to be the most effective of these therapies when analyzed separately.The multilayer bandage produces a gradient compression on the limb where distal pressure is higher than proximal pressure. Several materials are needed for the multilayer bandage, including tubular bandage lining, digit bandages, foam under-cast padding and multiple layers of short-stretch bandages to cover the entire limb. The Precast Adjustable Compression Wrap fits each patient through a Velcro system.

The aim is to compare the effectiveness of a precast adjustable compression wrap (Circaid) with the multilayer compression bandages in the treatment of the upper limb lymphedema.


Description:

The gold standard of the treatment of lymphedema is based on a combined program called complex decongestive therapy. The components of the complex decongestive therapy are skin care, kinesiotherapy, manual lymphatic drainage and compression. The compression with multilayer bandage has proved to be the most effective of these therapies when analyzed separately. With the multilayer compression bandage the upper limb lymphedema volume decreased a 37.2%.

The multilayer bandage produces a gradient compression on the limb where distal pressure is higher than proximal pressure. Several materials are needed for the multilayer bandage, including tubular bandage lining, digit bandages, foam under-cast padding and multiple layers of short-stretch bandages to cover the entire limb. The Precast Adjustable Compression Wrap fits each patient through a Velcro system.

Decreasing compression is achieved by controlling the tension applied to each Velcro through a visual color guide. The Precast Adjustable Compression Wrap has proved to be safe and effective to treat lower limb lymphedema, but there is little information about its effectiveness in the treatment of the upper limb lymphedema.

The aim is to compare the effectiveness of a precast adjustable compression wrap (Circaid) with the multilayer compression bandages in the treatment of the upper limb lymphedema.


Recruitment information / eligibility

Status Completed
Enrollment 47
Est. completion date April 5, 2017
Est. primary completion date January 19, 2016
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Upper limb lymphedema after axillary lymph node dissection for breast cancer.

- Lymphedema must affect at least the arm or the forearm.

- The lymphedema volume excess must be at least 10%

- The lymphedema must have not been previously treated or have been at least 1 year without treatment.

Exclusion Criteria:

- Bilateral upper limb lymphedema

- Cognitive or sensorial impairments which could interfere collaboration

- Plexopathy post radiotherapy

- Breast cancer in progression Pregnancy or Lactation

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Precast Adjustable Compression Wrap (Circaid)
A physiotherapist well trained in lymphedema treatment will apply a lymphatic drainage to the affected upper limb. Then the physiotherapist will apply the precast adjustable compression wrap to the patient. The patient would maintain the precast adjustable compression wrap until the next session of treatment. The first 10 sessions will be daily from Monday to Friday. After the 10 first sessions, the treatment will be applied on alternate days (3 per week) until the patient receive a tailored compression garment (7-14 days).
Multilayer Compression Bandages
A physiotherapist well trained in lymphedema treatment will apply a lymphatic drainage to the affected upper limb. Then the physiotherapist will apply the multilayer bandage to the patient. The patient would maintain the multilayer compression bandage until the next session of treatment. The first 10 sessions will be daily from Monday to Friday. After the 10 first sessions, the treatment will be applied on alternate days (3 per week) until the patient receive a tailored compression garment (7-14 days).

Locations

Country Name City State
Spain Germans Trias i Pujol Hospital Badalona Barcelona
Spain Hospital Vall Hebron Barcelona
Spain Hospital Universitari de Bellvitge Hospitalet de Llobregat Barcelona

Sponsors (4)

Lead Sponsor Collaborator
Parc de Salut Mar Germans Trias i Pujol Hospital, Hospital Universitari de Bellvitge, Hospital Vall d'Hebron

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in the excess of volume of upper limb Change in the excess of volume of the affected upper limb. The excess of volume is the difference in volume between the affected and the unaffected upper limb. The upper limb volumes will be obtained from the perimeters of the upper limbs and applying the truncate cone formula.
Baseline to 2 weeks (10 sessions of treatment). A follow up at 3 months
Baseline to 3 months (10 sessions of treatment)
Secondary Changes in pain, heaviness, tightness and hardness Changes in pain, heaviness, tightness and hardness will be measured by visual analogical scales. Baseline to 2 weeks (10 sessions of treatment). A follow up at 3 months Baseline to 3 months (10 sessions of treatment)
Secondary Changes in skin and lymphedema condition The skin and lymphedema condition will be evaluated every day along the treatment phase and at 3 months of follow up. Baseline to 2 weeks (10 sessions of treatment). A follow up at 3 months Baseline to 3 months (10 sessions of treatment)
Secondary Number of Participants with Serious and Non-Serious Adverse Events Collection of adverse effects spontaneously reported by the participants and/or observed by the investigators. In order to evaluate tolerability patients will be asked every day about any discomfort or troubles they could feel. On the other hand, it will be daily recorded how many hours the patient had used the precast adjustable compression wrap or the multilayer compression bandages. Baseline to 2 weeks (10 sessions of treatment). A follow up at 3 months Baseline to 3 months (10 sessions of treatment)
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