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Behavioural Intervention

Intervention-garment sleeve for Breast Cancer (L-Dex Trial)

N/A
Waitlist Available
Led By Andrea V Barrio, MD
Research Sponsored by Main Line Health
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 years
Awards & highlights

L-Dex Trial Summary

Primary Objective: To determine whether early intervention (with garment sleeve and gauntlet) in patients with pre-clinical lymphedema can halt the progression of lymphedema. Secondary Objectives:To evaluate whether bioimpedance is an accurate, reliable method to measure pre-clinical and clinical lymphedema. Tertiary Objective: To determine whether bioimpedance analysis is better than the gold standard of volume displacement to measure lymphedema. The successful completion of this study will address whether bioimpedance analysis is a reliable, accurate method to measure pre-clinical and clinical lymphedema. In addition, we intend to evaluate whether bioimpedance analysis is better than the gold standard of volume displacement for measuring lymphedema. And most importantly, we will evaluate whether a short trial of compression garments in women identified to have pre-clinical lymphedema can actually halt the progression of disease. Bryn Mawr Hospital would propose to publish the research and findings of this study, which may have future bearing on the post-operative therapeutic management of subjects with pre-clinical lymphedema following axillary surgery. Study Design:Randomized, Pilot Study

Eligible Conditions
  • Breast Cancer

L-Dex Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and 2 years for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
To determine whether early intervention in patients with pre-clinical lymphedema can halt the progression of lymphedema.
Secondary outcome measures
200 women will have bioimpedance and volume displacement measurements to evaluate whether bioimpedance is an accurate, reliable method to measure pre-clinical and clinical lymphedema as compared to standard (volume displacement)

L-Dex Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Intervention-garment sleeveExperimental Treatment1 Intervention
If the L-Dex is outside the normal range, or has increased 10 units from baseline, the patient will then be randomized to wear a compression sleeve (20 to 30 mm of Hg) daily for 4 weeks or observation (no sleeve). After 4 weeks, L-Dex measurements and water volume displacement will be reassessed in the treatment group.
Group II: ObservationActive Control1 Intervention
Observation arm will continue to be followed with serial L-Dex and water volume displacement methods.

Find a Location

Who is running the clinical trial?

Main Line HealthLead Sponsor
20 Previous Clinical Trials
6,579 Total Patients Enrolled
2 Trials studying Breast Cancer
186 Patients Enrolled for Breast Cancer
Sharpe-Strumia Research FoundationOTHER
7 Previous Clinical Trials
689 Total Patients Enrolled
Andrea V Barrio, MDPrincipal InvestigatorBryn Mawr Hospital

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~14 spots leftby Apr 2025