Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05977816

PROPEL-2: Prophylactic Negative Pressure Wound Therapy in Laparotomy Wounds

Led by Royal College of Surgeons, Ireland · Updated on 2024-10-26

2000

Participants Needed

11

Research Sites

154 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Post-operative wound issues in abdominal surgery have a significant impact on patient outcomes. This study is taking place to investigate if Negative Pressure Wound Therapy (NPWT) dressings reduces Surgical Site Infections, post surgical complications and improves scar appearance compared to standard dressings.

CONDITIONS

Official Title

PROPEL-2: Prophylactic Negative Pressure Wound Therapy in Laparotomy Wounds

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 years or older
  • Patient requires visceral abdominal surgery via a midline laparotomy
  • Patients who can complete questionnaires
Not Eligible

You will not qualify if you...

  • Patients who are unable to adhere to protocol requirements

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 11 locations

1

Mayo University Hospital

Castlebar, Ireland

Actively Recruiting

2

Beaumont Hospital

Dublin, Ireland

Actively Recruiting

3

Mater Misericordiae University Hospital

Dublin, Ireland

Actively Recruiting

4

St James's Hospital

Dublin, Ireland

Actively Recruiting

5

Tallaght University Hospital

Dublin, Ireland

Actively Recruiting

6

University Hospital Galway

Galway, Ireland

Actively Recruiting

7

Letterkenny University Hospital

Letterkenny, Ireland

Actively Recruiting

8

University Hospital Limerick

Limerick, Ireland

Actively Recruiting

9

Sligo University Hospital

Sligo, Ireland

Actively Recruiting

10

University hospital Kerry

Tralee, Ireland

Not Yet Recruiting

11

University Hospital Waterford

Waterford, Ireland

Actively Recruiting

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Research Team

C

Claire Donohoe, PhD, FRCSI

CONTACT

N

Noel Donlon, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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