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Post-operative Complication, Impulsive Compression, in Situ Bypass

NCT03192982 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2020-09-16

No results posted yet for this study

Summary

To investigate whether compression therapy with foot pump reduce post-operative edema, facilitate wound healing of operation wounds, promote healing of ischemic ulcers and shorten hospitalization, increase and improve the patient's subjective quality of life faster

Conditions

  • Compresion Therapy
  • Post-operative Edema
  • Wound Complication
  • Ischemia Limb
  • Quality of Life

Interventions

DEVICE

A-V impulse 6000 Series

foot pad and pump

DEVICE

Standard treatment (compression)

Short-stretch bandage from toes and up yo the upper thigh 40 mm Hg

Sponsors & Collaborators

  • Kolding Sygehus

    lead OTHER

Principal Investigators

  • Hans Ravn, MD PhD · Vejle Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-02-08
Primary Completion
2022-11-28
Completion
2022-11-30

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03192982 on ClinicalTrials.gov