Skip to content

A Study on antibiotic use in abdominal injury patients undergoing operation

Prophylactic antibiotic use in abdominal trauma patients undergoing operative intervention - A randomized control trial - PAAT

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/042088
Enrollment
100
Registered
2022-04-22
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: S369- Injury of unspecified intra-abdominal organ

Interventions

Intervention1: 24 hour regimen of prophylactic antibiotics in abdominal trauma patients undergoing operative intervention: 24 hours of Intravenous (I.V) INJ CEFOPERAZONE-SULBACTUM 2G TDS alongwith INJ

Sponsors

AIIMS New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.All patients who have sustained abdominal trauma and have underwent operative intervention within 24 hours of injury 2.Hemodynamically stable patients

Exclusion criteria

Exclusion criteria: 1.Patients with age 65 years 2.Patients with associated severe injuries such as open fractures , crushed/mangled extremities, vascular injuries, severe head injury or any other that requires prolonged antibiotic administration 3.Patients with co-morbidities like Hypertension, Diabetes, CKD, CLD, Immunocompromised state and coagulopathic disorders

Design outcomes

Primary

MeasureTime frame
To compare the rate of Surgical Site Infection (SSI) between 24 hour and 5 day antibiotic groups in abdominal trauma patients undergoing operative interventionTimepoint: Whenever signs of SSI show up or at 7,14,28 days postoperatively

Secondary

MeasureTime frame
To compare the 30 day mortality between both the antibiotic groupsTimepoint: 30 days;To compare the length of hospital stay between both the antibiotic groupsTimepoint: Till discharge;To compare the rate of non surgical site infections between both the antibiotic groupsTimepoint: Whenever the signs of non surgical site infections show up of at 7,14,28 days postoperatively;To compare the rates of readmission for SSI between both the antibiotic groupsTimepoint: Whenever the patient is readmitted due to SSI

Countries

India

Contacts

Public ContactDamodar Kakumanu

All India Institute of Medical Sciences, New Delhi

pratyushaaiims@yahoo.co.in7093703750

Outcome results

None listed

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