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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05509062
Other study ID # 22-0733
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 20, 2022
Est. completion date April 30, 2023

Study information

Verified date January 2024
Source University of Colorado, Denver
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to establish optimal guidelines for Manual Lymphatic Drainage in participants with lower extremity lymphedema.


Description:

To determine if there is a difference in L-Dex Score and Segmental Limb Volume in participants with lower extremity lymphedema as measured in liters by the SOZO machine between participants who receive Manual Lymphatic Drainage (MLD) techniques utilizing light tactile pressure with 5-10 mmHg without skin stretch versus medium tactile pressure of 11-20 mmHg and medium skin stretch with therapist in a stationary position, versus firm tactile pressure (> 21 mmHg) and maximal skin stretch with therapist weight shift.


Recruitment information / eligibility

Status Completed
Enrollment 64
Est. completion date April 30, 2023
Est. primary completion date April 30, 2023
Accepts healthy volunteers No
Gender All
Age group 30 Years to 75 Years
Eligibility Inclusion Criteria: - All adults between the age of 30 - 75 years - Lower extremity lymphedema Exclusion Criteria: - Pregnant women - Participants who are unable to stand independently for up to 2 mins - Participants who cannot make their own decisions - Participants undergoing cancer treatment - Participants with an Infection (active cellulitis) - Participants with a known Iodine Allergy - Participants who weigh more than 375 lbs - Participants with cardiac arrhythmias or implanted electronic equipment - Participants who have undergone joint replacement in involved extremity - Participants with cardiac insufficiency

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Pressure
Subjects are randomized to one of three treatment groups

Locations

Country Name City State
United States University of Colorado Anschutz Medical Campus Aurora Colorado

Sponsors (1)

Lead Sponsor Collaborator
University of Colorado, Denver

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in The L-dex (Lymphedema Index). The L-DEX score represents the difference in the amount of extracellular fluid in an at-risk limb compared to an unaffected limb. 18 months
Secondary Change in Total body weight in liters All the water within a person's body, including both intracellular and extracellular fluid. Expressed as volume (liters or pints) and percentage of total weight (%). 18 Months
Secondary Change in Extracellular Fluid in liters All fluid that is not contained within the cells. Expressed as volume (liters or pints) and percentage of TBW (%). 18 months
Secondary Change in Intracellular Fluid in liters • Description: All fluid contained within the cells. Expressed as volume (liters or pints) and percentage of TBW (%). 18 Months
Secondary Change in Skeletal Muscle Mass in lbs The amount of mass a person has that is made up of fat. Expressed in kgs or lbs and percentage of total weight (%) 18 Months
Secondary Change in Fat Mass in lbs The amount of mass a person has that is made up of fat. Expressed in kgs or lbs and percentage of total weight (%) 18 Months
Secondary Change in Free Fat Mass in lbs The amount of mass a person has that contains no fat (lean body mass). Includes muscle, connective tissue, organs, body water and bone. Expressed in kgs or lbs and percentage of total weight (%). 18 Months
Secondary Change in Basal Metabolic Rate (BMR) in lbs Daily amount of energy a person's body burns when at complete rest. Expressed in calories. 18 Months
Secondary Change in Basal Metabolic Rate in kg/m^2 A relationship between weight and height that is associated with body fat and health risks. BMI = weight / height2. 18 months
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