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Can Using a Negative Pressure Drain Reduce Infection Risk After Abdominal Surgery?

Efficacy Of Subcutaneous Closed Suction Drain In Reduction Of Postoperative Surgical Site Infection In Midline Exploratory Laparotomies - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/089353
Enrollment
80
Registered
2025-06-23
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Subcutaneous Negative suction drain during abdominal wall closure: Negative suction drain (romovac) will be placed in subcutaneous plane during abdominal wall closure after midline lapa

Sponsors

Institutional supply government
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age group above 18 years. Patients undergoing emergency and elective midline laparotomy surgeries with class III or IV wound.

Exclusion criteria

Exclusion criteria: Patients less than 18 years or above 80 years. Patients with immunocompromised status like HIV, radiotherapy, or chemotherapy. Re-done laparotomy surgeries. Patients undergoing emergency and elective midline laparotomy surgeries with class II wound. Not giving consent to participate in study.

Design outcomes

Primary

MeasureTime frame
To assess the efficacy of subcutaneous closed suction wound drainage in the reduction of SSIs in class III and class IV surgical wounds.Timepoint: 30 days

Secondary

MeasureTime frame
To assess the role of predictive factors in wound infection like diabetes.Timepoint: 30 days;To compare the rate of SSI between elective and emergency midline explorative laparotomy surgeries. Timepoint: 30 days;To identify the most common organism in SSIs. Timepoint: 30 days

Countries

India

Contacts

Public ContactDr Anis Vohra

BMC and SSG hospital Baroda

asvohra123@gmail.com9824267069

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026