MedTrace Logo

Oxygen Wound Therapy Feasibility Study

NCT05422248 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2023-09-13

No results posted yet for this study

Summary

Determine the feasibility of using a new topical oxygen therapy device to treat hard to heal lower leg wounds.

Conditions

  • Chronic Leg Ulcer

Interventions

DEVICE

Series Topical Oxygen Therapy

Standard care provided to the whole wound followed by intervention device care to the whole wound.

DEVICE

Paired Topical Oxygen Therapy

Care provided to one portion of wound by intervention device and standard care to remaining portion of wound.

Sponsors & Collaborators

  • Fisher and Paykel Healthcare

    lead INDUSTRY

Principal Investigators

  • Jolanta Krysa · Southern DHB Vascular Surgery

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-12-01
Primary Completion
2025-12-01
Completion
2026-08-01

Countries

  • New Zealand

Study Locations

More Related Trials

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 NCT05422248 on ClinicalTrials.gov