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Effectiveness of Negative Pressure Wound Therapy in the community

Effectiveness of Negative Pressure Wound Therapy in the Community: Wound closure of post surgical wounds post hospital discharge

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625000618459
Enrollment
60
Registered
2025-06-13
Start date
2025-07-25
Completion date
2025-11-28
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This study is to determine the efficacy of use of single use Negative Pressure Wound Therapy products in the community at varying pressures to determine which device would effectively heal patient wounds more rapidly and that is comfortable and easy to apply.

Interventions

Intervention - application of a negative pressure device of -125mmHg on post acute wounds by a clinical nurse Duration- the patient will be trialled with the product for 2 to 4 weeks with frequency of dressing changes determined by the clinical nurse. The location of the trial will be conducted within the community in the clients home and will need to be located within the Metro South Health and Hospital catchment. Monitoring will be conducted through reviewing patient chart. The pressures are s

Intervention - application of a negative pressure device of -125mmHg on post acute wounds by a clinical nurse Duration- the patient will be trialled with the product for 2 to 4 weeks with frequency of dressing changes determined by the clinical nurse. The location of the trial will be conducted within the community in the clients home and will need to be located within the Metro South Health and Hospital catchment. Monitoring will be conducted through reviewing patient chart. The pressures are set for each device and the pressure cannot be titrated. Group allocation will be determined through the choice of participants and at the discretion of the clinical nurses.

Sponsors

MolnLycke
Lead SponsorCommercial sector/Industry

Study design

Allocation
Non-randomised trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Wound referrals received from hospitals within the Metro South catchment area. Wounds that are post surgical (ie incision and drainage of abscess, surgical dehiscence) People who have a wound over the age of 18 years People who reside within their own home within the community People with a medicare card

Exclusion criteria

People < 18 years People with chronic wounds who have a longer healing trajectory People who live in nursing homes

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026