Investigating the rate of surgical site infection in two methods of continuous and discrete sutures for primary wound closure in gastric and intestinal surgeries at the independent educational-therapeutic center Velayat in Qazvin: A randomized clinical trial study

Not Applicable

Recruiting

• Conditions: Infection at the surgical suture site.; Infection following a procedure; T81.4

• Registration Number: IRCT20230826059259N1
• Lead Sponsor: Qazvin University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 16 October 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 154

Inclusion Criteria

Patients undergoing gastric and intestinal surgery
Age range 18-80

Exclusion Criteria

Having diabetes
Immune system diseases
History of gastrointestinal surgery
Pregnancy
Smoking, drugs and alcohol
Hypoproteinemia

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Accumulation of pus under the skin. Timepoint: From the time of completion of surgery to thirty days after that. Method of measurement: Clinical examination by a doctor.;Active secretions from the wound surface. Timepoint: From the time of completion of surgery to thirty days after that. Method of measurement: Clinical examination by a doctor.;Leukocytosis (white blood cells less than 4500). Timepoint: From the time of completion of surgery to seven days after that. Method of measurement: CBC test.;Pain at the wound site. Timepoint: From the time of completion of surgery to thirty days after that. Method of measurement: McGill pain questionnaire.;Fever. Timepoint: From the time of completion of surgery to thirty days after that. Method of measurement: Clinical examination by a doctor.