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EdemaWear to Reduce Edema in Hospitalized Patients With CVI:

Primary Purpose

Chronic Venous Insufficiency

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Edema Wear fuzzy wale compression garment
Sponsored by
Massachusetts General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Chronic Venous Insufficiency focused on measuring Chronic Venous Insufficiency, CVI

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • history of CVI (Clinical classification 1-5), with > 2+ edema of the lower legs,
  • > 2+ peripheral pulses (popliteal, dorsalis pedis [DP], and posterior tibial [PT]) or audible biphasic / triphasic Doppler signal, if pulses not palpable.

Exclusion Criteria:

  • open venous stasis ulcer(s) or other wounds on lower legs
  • lymphedema or risk factors for lymphedema
  • acute heart failure with active management
  • known deep vein thrombosis (DVT) with subtherapeutic anticoagulation
  • peripheral arterial disease (PAD) with reduced / absent pulses
  • known or suspected inferior vena caval (IVC) compression
  • circumference of lower leg < 45 cm or > 115 cm (size limits of small and extra-large EdemaWear®)
  • severely altered mental status or lacking capacity to consent.

Sites / Locations

  • Massachusetts General Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Edema Wear

Arm Description

Edema Wear fuzzy wale compression garment worn on lower extremities continuously for 5 days or until discharge if less than 5 days.

Outcomes

Primary Outcome Measures

change in lower leg volume
Difference between volume of lower leg / foot between Day 1 and Day 5 (or day of hospital discharge if less than 5 days)

Secondary Outcome Measures

Full Information

First Posted
April 3, 2019
Last Updated
March 21, 2023
Sponsor
Massachusetts General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03904602
Brief Title
EdemaWear to Reduce Edema in Hospitalized Patients With CVI:
Official Title
EdemaWear to Reduce Edema in Hospitalized Patients With Chronic Venous Insufficiency: A Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Terminated
Why Stopped
Patients experienced translocation of edema from lower extremities to trunk heightening concern about triggering congestive heart failure in frail elders.
Study Start Date
August 19, 2019 (Actual)
Primary Completion Date
September 15, 2019 (Actual)
Study Completion Date
September 15, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes

5. Study Description

Brief Summary
The purpose of this pilot study is to evaluate the effectiveness of EdemaWear® fuzzy wale longitudinal compression stockings on reducing lower extremity edema in hospitalized adult patients with a history of CVI who are at high risk of consequent venous leg ulcers (VLU) and patient experience with continuously wearing Edema Wear for up to five days
Detailed Description
Hospitalized patients with chronic venous insufficiency (CVI) are at high risk of venous leg ulcers (VLU) due to lower leg edema and skin changes. Since VLU are associated with prolonged morbidity and appreciable financial burden to the patient and society, prevention of VLU by reduction of lower leg edema is paramount. Although the mainstay of VLU prevention is compression, there is a gap in the acute care toolbox to manage the symptom of CVI edema. Currently, ACE bandages are the single most common 'compression wraps' stocked on inpatient units. The disadvantages of ace wraps, which are long-stretch bandages, are two-fold: 1) lower working pressure impeding venous return to the heart, and 2) higher resting pressure that may cause a tourniquet effect and consequent tissue ischemia. A newer moderately-priced mild compression product (15-20 mmHg), EdemaWear® longitudinal elastic compression stockinet, offers an alternative for hospitalized patients. There is limited evidence about the effectiveness of EdemaWear® (that is, modest reduction of lower leg edema) derived from one case series and two comparative evaluations involving only patients in out-patient clinics. This pilot study will expand the evidence related to the effectiveness of EdemaWear® in reducing lower leg edema to include hospitalized patients with CVI. . The proposed pilot interventional study which involves a single-group repeated measures design with mixed methods has three aims: evaluate the effectiveness of EdemaWear fuzzy wale elastic compression stockinet in reducing lower extremity edema in hospitalized adult patients with chronic venous insufficiency as measured by the difference in the volume of each lower extremity from Day 1 and Day 5 of data collection or the day of discharge if it occurs in less than five days determine through interviews the experience of patients continuously wearing EdemaWear compression garment for up to five days or hospital discharge if it occurs in less than five days qualitatively describe nurses' perceptions of their patients experience with continuously wearing EdemaWear compression garment for up to five days or hospital discharge if it occurs in less than five days The procedure: Initial data collection related to demographic variables (age, gender, race, ethnic background), primary diagnosis, comorbid conditions (Charlson Comorbidity Index), CEAP classification of chronic venous disease, medication / treatment regimen, degree of lower extremity edema, volume of lower leg peripheral pulses, ankle-brachial indexes Daily data collection related to changes in health status and treatment Daily measurement of the girth of both lower extremities at 10 cm intervals from mid-foot, up the legs, to just below the knees. Daily interviews of patient and nursing staff related to experience of continuously wearing EdemaWear for up to five days or hospital discharge if it occurs in less than five days Data analysis: - Descriptive statistics will be performed on demographic and physiological variables, including number / percent for nominal variables and mean (+SD) for continuous variables. Data will be analyzed to decide whether they meet the assumptions of the planned analyses. Repeated measures ANOVA will be used to determine whether there are significant differences in the volume of the lower legs treated with EdemaWear® across the five time periods. The alpha level will be set at p < .05. Qualitative data from daily interviews of patients and nursing staff will be analyzed by the PI and Co-Is of this study. Content analysis will be used to analyze the data. The unit of analysis will be phrases or sentences contained in responses to questions in the Interview Guides. Content Analysis is a qualitative research method that is used to isolate and interpret themes, issues, and repeated patterns. They refine understanding as new insights about the data emerge. The strategies for analysis outlined by Downe - Wamboldt will be followed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Venous Insufficiency
Keywords
Chronic Venous Insufficiency, CVI

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
3 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Edema Wear
Arm Type
Experimental
Arm Description
Edema Wear fuzzy wale compression garment worn on lower extremities continuously for 5 days or until discharge if less than 5 days.
Intervention Type
Device
Intervention Name(s)
Edema Wear fuzzy wale compression garment
Intervention Description
net-like compression structure of Lycra spandex elastic yarn with longitudinal fuzzy wales (similar to corduroy fabric)
Primary Outcome Measure Information:
Title
change in lower leg volume
Description
Difference between volume of lower leg / foot between Day 1 and Day 5 (or day of hospital discharge if less than 5 days)
Time Frame
up to 5 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: history of CVI (Clinical classification 1-5), with > 2+ edema of the lower legs, > 2+ peripheral pulses (popliteal, dorsalis pedis [DP], and posterior tibial [PT]) or audible biphasic / triphasic Doppler signal, if pulses not palpable. Exclusion Criteria: open venous stasis ulcer(s) or other wounds on lower legs lymphedema or risk factors for lymphedema acute heart failure with active management known deep vein thrombosis (DVT) with subtherapeutic anticoagulation peripheral arterial disease (PAD) with reduced / absent pulses known or suspected inferior vena caval (IVC) compression circumference of lower leg < 45 cm or > 115 cm (size limits of small and extra-large EdemaWear®) severely altered mental status or lacking capacity to consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Virginia Capasso, PhD, APRN
Organizational Affiliation
Massachusetts General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Massachusetts General Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26358303
Citation
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25047584
Citation
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Links:
URL
https://woundcareadvisor.com/best-practices-vol2-no6/
Description
Bjork R. The long and short of it: Understanding compression bandaging. Wound Care Advisor. 2013; 2(6).
URL
https://compressiondynamics.com/
Description
EdemaWear® New Compression Textile.
URL
https://compressiondynamics.com/wp-content/uploads/2015/06/PosterFuzzy-Wale-Elastic-Compression-as-a-Tool-in-Reducing-Lower-Extremity-Edema-and-Accompanied-Fluid-Accumulation..pdf
Description
Livingston M, Ross, S. Fuzzy Wale Longitudinal Elastic Compression as a Tool in Reducing Lower Extremity Edema and Accompanied Fluid Accumulation. Poster, 2014.
URL
https://compressiondynamics.com/wp-content/uploads/2015/06/Poster-A-Comparison-of-Fuzzy-Wale-Longitudinal-Elastic-Compression-to-Elasticated-Tubular-Bandage-Compression-as-a-Tool-in-Reducing-Lower-Extremity-Edema.pdf
Description
Poster-A-Comparison-of-Fuzzy-Wale-Longitudinal-Elastic-Compression-to-Elasticated-Tubular-Bandage-Compression-as-a-Tool-in-Reducing-Lower-Extremity-Edema.pdf
URL
https://compressiondynamics.com/wp-content/uploads/2018/05/PosterComparative-Evaluation-of-the-Clinical-Effectiveness-of-Two-Elastic-Compression-Stockinets-for-the-Treatment-of-Lower-Limb.pdf
Description
PosterComparative-Evaluation-of-the-Clinical-Effectiveness-of-Two-Elastic-Compression-Stockinets-for-the-Treatment-of-Lower-Limb.pdf
URL
https://www.sralab.org/rehabilitation-measures/
Description
numeric-pain-rating-scale

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EdemaWear to Reduce Edema in Hospitalized Patients With CVI:

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