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Negative Pressure Wound Therapy. Therapy Effects and the Impact on the Patient's Quality of Life

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Karolinska Institute

Status

Terminated

Conditions

Wounds

Treatments

Procedure: VAC treatment
Procedure: Conventional treatment

Study type

Interventional

Funder types

Other

Identifiers

NCT01191567
2008/2023-31

Details and patient eligibility

About

Wounds have long been a source of suffering for unfortunate victims and in recent years new complementary methods have been developed in areas where traditional wound treatment has been insufficient. Treating wounds with negative pressure, Vacuum assisted closure® [VAC], is a relatively new method of treatment and knowledge about its effect on patients is limited.

Earlier studies haven't been able to answer the question about which groups of patients that are in most favour of the treatment and what impact the treatment has on the patient's quality of life.

It is important with further research since an effective and mild wound treatment can decrease suffering and increase quality of life for the patient. Wound treatment that does not lead to an achieved treatment goal can lead to a risk for the patient and should be avoided.

The project consists of 4 part studies: Study 1 and 2 are chart review studies of a consecutive series of patients treated with VAC at Södersjukhuset during a 3 year period. The patients are described on the basis of medical, surgical and demographical factors. Outcome is treatment results and risk factors for a treatment failure.

Study 3 and 4 are clinical randomised studies with the aim of studying whether treatment with VAC provides a faster and more effective healing of acute and postoperative wounds, and in what way the treatment affect the quality of life and pain of the patients, compared to conventional treatment.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • acute wounds with substance defect after primary suture demanding further treatment or wounds not primary sutured
  • wounds with osteosynthesis, bone or tendon visual regardless wound size
  • postoperative infections with wound and substance defect demanding further treatment.
  • fasciotomy on extremity

Exclusion criteria

  • wound size < 2 cm and depth < 1 cm
  • pressure ulcers, open abdomen and chronic ulcers
  • patients with dementia or mental illness so severe that participation in the study is impossible
  • patients non in command of the swedish language
  • ongoing treatment with warfarin

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 2 patient groups

Conventional treatment
Active Comparator group
Treatment:
Procedure: Conventional treatment
VAC treatment
Experimental group
Treatment:
Procedure: VAC treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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