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Utilization of Compreflex Wraps in Patients With Chronic Venous Insuffciency

NCT05364112 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2022-10-25

No results posted yet for this study

Summary

This is a multicentre, quasi-experimental study to evaluate the Conformitè Europëenne-marked Compreflex standard calf and foot (with basic liner) under routine conditions.

The study will be conducted at 4 clinics and will include 100 consecutive patients. Patients will be followed-up until 26 weeks.

Conditions

  • Varicose Ulcer
  • Venous Insufficiency of Leg

Interventions

DEVICE

Compreflex

The Compreflex standard calf and foot (with basic liner) from Sigvaris (St. Gallen, Switzerland) is an easy-to-use interlacing Velcro wrap device with adjustable compression levels.

Sponsors & Collaborators

  • SULTAN AHMAD SHAH MEDICAL CENTRE @ IIUM

    collaborator UNKNOWN

  • Universiti Kebangsaan Malaysia Medical Centre

    collaborator OTHER

  • University of Malaya

    collaborator OTHER

  • Kuala Lumpur General Hospital

    lead OTHER_GOV

Principal Investigators

  • Harikrishna R Nair · Kuala Lumpur General Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-09-01
Primary Completion
2022-12-31
Completion
2022-12-31

Countries

  • Malaysia

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 NCT05364112 on ClinicalTrials.gov