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Diabetes (Insulin-requiring, Type 1 or Type 2)NCT07392853

Investigation of the Effectiveness of Prophylactic NPWT (ciNPWT) in High-risk Diabetic Patients With Acute Laparotomy Wounds

A study testing Prophylactic/Incisional Negative Pressure Wound Therapy in people with Diabetes (Insulin-requiring, Type 1 or Type 2), run by Semmelweis University at 1 site in Hungary.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The aim of this study is to evaluate the effectiveness of prophylactic Negative Pressure Wound Therapy (NPWT) in patients with diabetes mellitus undergoing laparotomy who are at high risk for Surgical Site Infections (SSI). Read more about this study

Who is it for?
Any age
What is being tested?
Prophylactic/Incisional Negative Pressure Wound Therapy
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
110 participants
Where
1 siteHungary
Study dates
22 Feb 2026to 22 Mar 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

None listed.

Who cannot join

  • Pregnancy,
  • Disseminated cancer (irresectable distant metastasis, peritoneal carcinomatosis),
  • Life expectancy of less than 30 days,
  • Refusal to participate in the study.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Hungary1 site
  • Semmelweis University, Department of Surgery, Transplantation and Gastroenterology

    Budapest, 1082

    Balazs Banky, +36-20-825-8915, bankybalazs@gmail.com

    Andras Herczeg, +36-20-670-1721, herczeg.andras.ivan@semmelweis.hu

Other trials in Hungary

About this study

Official title: Investigation of the Effectiveness of Prophylactic NPWT (ciNPWT) in High-risk Diabetic Patients With Acute Laparotomy Wounds - A Randomized, Prospective Clinical Trial

The aim of this study is to evaluate the effectiveness of prophylactic Negative Pressure Wound Therapy (NPWT) in patients with diabetes mellitus undergoing laparotomy who are at high risk for Surgical Site Infections (SSI). In addition to clinical efficacy, the investigators also plan a cost effectiveness analysis to assess the applicability of this relatively high-cost intervention in a domestic healthcare setting.

Read the detailed description

Background and Introduction Postoperative surgical site infections (SSI) continue to represent a significant challenge across almost all surgical disciplines, despite the widespread implementation of well-established aseptic and preventive measures. Abdominal surgery, in particular, presents an inherently higher risk, considering the nature of the procedures (e.g., surgeries involving bowel resections). For emergency and urgent procedures, the rate of wound infections can reach as high as 30%, according to some literature sources.

Risk Factors for SSI Risk factors can be categorized based on the surgical procedure itself (e.g., acute/elective, bowel resection/non-resection, wound cleanliness), patient characteristics (e.g., diabetes, smoking, peripheral arterial disease, obesity, age, gender), underlying medical conditions (e.g., cancer, immunosuppressed or septic patients), and perioperative management (e.g., surgical duration, transfusion requirements, hypothermia, hyper/hypoglycemia, hypoxia, pharmacological treatments). Many of these factors are modifiable during patient care (e.g., achieving normothermia, ensuring proper asepsis during surgery, maintaining normoglycemia) or preoperatively (e.g., improving nutritional status, correcting anemia, managing chronic diseases such as diabetes and hypertension, promoting weight reduction). However, in emergency surgeries, there is often insufficient time to address these factors, significantly increasing the risk of SSI.

The Impact of Diabetes Mellitus as an SSI Risk Factor Uncontrolled diabetes is associated with a higher incidence of complications, including wound infections. Factors such as tissue hypoxia (due to diabetic micro- and macroangiopathy and impaired angiogenesis), cellular dysfunction (e.g., abnormal endothelial, macrophage, and neutrophil function), and the formation of glycotoxins (Advanced Glycation End-products or AGEs) due to hyperglycemia impair wound healing. Numerous large-scale meta-analyses have confirmed the association between diabetes and surgical wound infections . Studies across various surgical fields (e.g., cardiac surgery, orthopedics, colorectal surgery) have demonstrated that preoperative (HbA1c) and perioperative (normoglycemia) management of blood glucose levels can significantly reduce the risk of SSI .

ciNPWT (Closed Incisional, Prophylactic NPWT) as a Method for Preventing Surgical Site Infections

Negative Pressure Wound Therapy (NPWT) was initially developed in the 1990s to treat chronic, difficult-to-heal wounds (Argenta \& Morykwas). The mechanism of NPWT involves the application of either continuous or intermittent negative pressure, which increases tissue vascularization, reduces edema, and promotes wound healing by removing necrotic tissue debris and stimulating granulation tissue formation. When applied prophylactically to closed surgical incisions, the available literature supports the significant reduction of septic surgical complications. Based on the results of a previously published multicenter, randomized, prospective clinical trial conducted by the investigators' research team, ciNPWT has been shown to reduce the incidence of SSIs following high-risk, urgent general abdominal surgeries (2). However, in that study, few poorly controlled diabetic patients were included, meaning no conclusions could be drawn specifically regarding this high-risk group. The effectiveness of NPWT has been largely settled in clinical debate, with numerous studies demonstrating its positive impact on wound healing. However, the cost-effectiveness of prophylactic NPWT remains an open question.

Being tested
Prophylactic/Incisional Negative Pressure Wound Therapy
Keywords
abdominal surgery, SSI, diabetes, emergency surgery, ciNPWT
Medical subject headings
Diabetes Mellitus

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Prophylactic/Incisional Negative Pressure Wound TherapyDevice

    Negative Pressure Wound Therapy device used on closed laparotomy wound to prevent SSI.

Study groups in NCT07392853
Study groupRoleWhat they receive
ciNPWTExperimentalGroup of patients being treated with prophylactic NPWT after emergency laparotomy.
Receives: Device: Prophylactic/Incisional Negative Pressure Wound Therapy
ControlNo interventionGroup of patients being treated with "regular" wound dressing.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Incidence of SSI

    The ratio of patients developing surgical site infection after emergency laparotomy.

    Unit of Measure: Number and percentage of patients Measurement Tool : Clinical assessment and medical records

    Measured: 30 days

Secondary outcomes (7)
  1. Length of Intensive Care Unit (ICU) stay

    Number of days spent in the Intensive Care Unit following surgery. Unit of Measure: Days Measurement Tool: Hospital medical records

    Measured: 30 days

  2. Length of hospital stay

    Total number of days of hospitalization following surgery.

    Unit of Measure: Days Measurement Tool: Hospital medical records

    Measured: 30 days

  3. Incidence of abdominal wall dehiscence

    Occurrence of abdominal wall dehiscence following surgery.

    Unit of Measure: Number and percentage of patients Measurement Tool : Clinical assessment and medical records

    Measured: 30 days

  4. Reoperation rate

    Proportion of patients requiring at least one reoperation following the index procedure.

    Unit of Measure: Number and percentage of patients (Yes/No)

    Measurement Tool: medical records

    Measured: 30 days

  5. Number of reoperations per patient

    Total number of reoperations performed per patient during the study period.

    Unit of Measure: Count

    Measurement Tool: medical records

    Measured: 30 days

  6. Quality of life assessed by EQ-5D questionnaire

    Health-related quality of life assessed using the EQ-5D questionnaire.

    Unit of Measure: Score

    Measurement Tool: EQ-5D questionnaire

    Measured: 30 days

  7. Direct healthcare costs

    Direct healthcare costs associated with postoperative care and complications.

    Unit of Measure: Hungarian Forint (HUF)

    Measurement Tool: Hospital billing and accounting records

    Measured: 30 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Feb 2026
  2. Study start22 Feb 2026 (estimated)
  3. Primary completion22 Feb 2026 (estimated)
  4. Study completion22 Mar 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
110 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07392853
Sponsor's protocol ID
BM/30843-3/2025
Status last verified
Jan 2026
First submitted
24 Jan 2026
Last updated
6 Feb 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: We apply strict regulations for the secure handling of IPD during the study. The data are used solely for the purposes of the research, and sharing them with other researchers could increase privacy risks.

Questions about this trial

What is this clinical trial studying?

A study testing Prophylactic/Incisional Negative Pressure Wound Therapy in people with Diabetes (Insulin-requiring, Type 1 or Type 2), run by Semmelweis University at 1 site in Hungary.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 0 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 6 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Hungary. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Balázs Bánky (+36-20-825-8915, bankybalazs@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Incidence of SSI (time frame: 30 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Feb 2026.

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Clinical Trial NCT07392853 | AzTrials