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Clinical Trials/IRCT20201022049115N1
IRCT20201022049115N1
Completed
未知

Evaluation of the effect of subcutaneous implantation of Corrugated drain in reducing the incidence of surgery side infection in patient with midline incision

Tehran University of Medical Sciences0 sites158 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Condition 1: Acute abdomen. Condition 2: Acut peritonitis. Condition 3: Biliary peritonitis. Condition 4: Fecal peritonitis.
Sponsor
Tehran University of Medical Sciences
Enrollment
158
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients diagnosed with acute peritonitis who have undergone acute midline incision surgery
  • Patients with biliary peritonitis, fecal peritonitis, or patients with obvious pus in the peritoneal cavity
  • Patients with subcutaneous fat thickness of more than 20 mm

Exclusion Criteria

  • Patients under 18 years old and over 70 years old
  • Patients who do not consent to participate in the study
  • Patients who undergo surgery with incisions other than midline incisions (McBurney incision, cochlear incision, paramedin incision, etc.)
  • Pregnant patients
  • Immune deficiency patients (patients with HIV positive serology, patients undergoing immunosuppressive therapy and patients undergoing any chemotherapy in the last 3 months)
  • Patients for whom any other implant except drain is implanted (including meshplasty, etc.)
  • Patients who do not visit the clinic at the appointed times for follow up
  • Patients with a subcutaneous fat thickness of less than 20 mm
  • Patients with other types of peritonitis (pancreatic peritonitis, etc.)

Outcomes

Primary Outcomes

Not specified

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