Skip to main content
Clinical Trials/IRCT201206165485N3
IRCT201206165485N3
Completed
Phase 2

Comparing the effects of conventional surgery with resection of a layer of dermis and epidermis on decreasing the rate of surgical wound infection and dehiscence in high risk patients operated for obstetric or gynecologic conditions

Vice chancellor for research, Women's Reproductive Health Research Center0 sites740 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
wound infection.
Sponsor
Vice chancellor for research, Women's Reproductive Health Research Center
Enrollment
740
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Vice chancellor for research, Women's Reproductive Health Research Center

Eligibility Criteria

Inclusion Criteria

  • patient with moderate to severe obesity (BMI\=30\-40\) , subcutaneous fat thickness over 5 cm, diabetes, suppressed immunity, systemic and chronic illnesses, cesarean section for meconium defecation, ruptured membrane, prolonged labor and dystocia, cesarean lasting more than 2 hours, gynecologic operations lasting more than 3 hours, presence of scars in the operative field
  • Exclusion criteria: patient with bleeding illnesses, cardiovascular diseases or critical conditions requiring to urgently terminate the operation, active infection like bacteremia, septicemia, pelvic or abdominal abscess, chorioamnionitis, acute PID, severe bleeding, cancer

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Similar Trials