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

PROPEL-2 Prophylactic Negative Pressure Wound Therapy (NPWT) in Laparotomy Wounds: a Randomised Controlled Trial Comparing Negative Pressure Wound Therapy to Standard Wound Management in Patients Following Midline Laparotomy

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05977816
Acronym
PROPEL-2
Enrollment
2000
Registered
2023-08-04
Start date
2023-07-14
Completion date
2026-07-31
Last updated
2024-10-26

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

Conditions

Wound Surgical, Wound Infection, Cosmesis

Keywords

Negative Pressure Wound Therapy, Surgical site Infection, Laparotomy, Post-operative Complications, Abdominal Incision, health economics, POSAS, CoPaQ

Brief summary

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.

Detailed description

NPWT dressings are designed to remove and absorb any fluid leaking from the wound. This might reduce surgical site infections, improve wound healing and improve scar appearance compared to using standard dressings. Data is limited in the application of NPWT dressings to laparotomy incisions in the acute and elective care surgery setting. Surgical site infections can complicate a patient's post-operative course significantly, often necessitating a longer length of stay, antibiotic therapy, intervention for wound collections and impair patient mobility and overall recovery. In addition to this, laparotomy wound complications can possibly delay adjuvant therapy and also increases healthcare costs both as an inpatient and in the community. Despite significant measures to reduce such complications in the form of wound care bundles, changing of gloves prior to wound closure etc., surgical site complications continue to represent a huge healthcare burden. The Investigators are conducting this study to determine whether NPWT dressings reduce surgical site infections, improve wound healing and scar appearance. This study will also involve a cost-based analysis and seek information from patients on their quality of life. Results from this study will provide evidence on whether these dressings should be used as standard of care for management of surgical laparotomy wounds.

Interventions

DEVICENegative Pressure Wound Therapy

Application of a negative wound pressure therapy dressing to the wound post laparotomy

Application of a standard wound dressing to the wound post laparotomy

Sponsors

Royal College of Surgeons, Ireland
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Parallel Assignment

Eligibility

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

Inclusion criteria

* Aged 18 years or older * Patient requires visceral abdominal surgery via a midline laparotomy * Patients who can complete questionnaires

Exclusion criteria

• Patients who are unable to adhere to protocol requirements

Design outcomes

Primary

MeasureTime frameDescription
Rate of Surgical Site Infection (SSI)1 month following surgeryTo compare the rate of surgical site infections within 1 month of the surgical procedure, using Negative Pressure Wound Therapy compared to standard dressings. SSIs will be classified according to Centre for Disease Control (CDC) criteria.

Secondary

MeasureTime frameDescription
Scar assessment - using the Patient and Observer Scar Assessment Scale (POSAS)1 month following surgeryThe POSAS is made up of two scales: the patient scale and the observer scale; each of the six components is scored numerically on a scale of 1 to 10. The component scores are then added together; the worst scar would receive a score of 60, while the best scar would receive a score of 6
Health-related out-of- Pocket Costs assessed using the Costs for Patients Questionnaire (CoPaQ)1 monthThe CoPaQ measures patient and caregivers out-of-pocket expenses (direct and indirect) associated with a health condition
Health-related quality of life with the EuroQol-5 dimensions five level index questionnaire (EQ-5D-5L)BaselineThe questionnaire covers five dimensions of health: mobility, self-care, usual activities, pain or discomfort, and anxiety or depression. Each dimension has 5 levels: no problems (1), slight problems (2), moderate problems (3), severe problems (4) and extreme problems (5). The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. The raw scores are also converted to an EQ-5D index value using a scoring algorithm (British tariff) ranging from -0.594 (worst perceived health state) to 1.00 (best perceived health state)
Healthcare incremental cost- utility ratio6 monthsThe incremental cost-effectiveness ratio at 6 months for NPWT vesus standard dressings for patients undergoing laparotomy.The effectiveness will be expressed as quality adjusted life years (QALYs) in a cost-utility analysis. QALYs are a composite measure of outcomes where utilities for health states (on 0-1 scale, where 0 corresponds to death and 1 to full health) act as qualitative weights to combine quantity and quality of life. The number of QALYs in each group will be assessed with the EuroQol 5 Dimensions questionnaire (EQ5D). The EQ-5D measures health status in terms of mobility, self-care, usual activities, pain/discomfort and anxiety/depression
Healthcare cost-effectiveness ratio at 6 months6 monthsAssessment of the cost-effectiveness ratio at 6 months between NPWT dressings compared to standard dressings. The criteria of effectiveness used will be; Length of hospital stay, requirement for return to theatre, requirement for critical care and number of dressings used
Health Economics evaluation of resource use and cost effectiveness using Negative Pressure Wound Therapy dressings6 monthsInvestigating resource use and cost effectiveness of single-use, prophylactic negative pressure wound therapy versus standard dressings for midline laparotomy wounds based on length of hospital stay and costs of dressings

Countries

Ireland

Contacts

Primary ContactClaire Donohoe, PhD, FRCSI
Cldonohoe@stjames.ie35314103000
Backup ContactNoel Donlon, PhD
donlonn@tcd.ie35314103000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026