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Vacuum-Assisted Dressings (V-AD) in the Management of Open Chest Wounds

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Mayo Clinic

Status

Completed

Conditions

Open Chest Wounds

Treatments

Device: Wound Vacuum-assisted dressing
Other: Control group

Study type

Interventional

Funder types

Other

Identifiers

NCT02803164
16-002486

Details and patient eligibility

About

Vacuum-assisted dressings (V-AD) are effective in treating patients with open chest wounds (OCW) and will decrease the time-to-closure of such wounds when compared to a historical cohort of patients managed by traditional wound care management.

Enrollment

21 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subject is scheduled to undergo surgical intervention(s) as part of the standard care for management of intra-thoracic infection.

Exclusion criteria

  • Patent bronchopleural fistulas. Severe respiratory failure requiring mechanical ventilation at the time of first consultation.
  • Proven or suspected malignancy in the wound. Coagulopathy due to medical or pharmacologic reasons. Dependency on anticoagulants or antiplatelet medication due to high risk for adverse events if these medications are stopped for a prolonged period of time.

Allergy to acrylic products.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

21 participants in 2 patient groups

Vacuum-assisted dressing
Other group
Description:
Eligible subjects will receive negative pressure wound therapy during surgery.
Treatment:
Device: Wound Vacuum-assisted dressing
Historical control group for comparison
Other group
Description:
Retrospective review of subjects medical records with open chest wounds who were treated with the traditional treatment techniques.
Treatment:
Other: Control group

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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