Efficacy of Low Level Laser Therapy on The Post Midline laparotomy Wound Pai
Not Applicable
Recruiting
- Registration Number
- IRCT20221018056225N1
- Lead Sponsor
- Bagheiat-allah University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Patients who are in the age range of 30 to 60 years.
Patients who underwent midline laparotomy were selected for elective upper and lower gastrointestinal surgery.
Exclusion Criteria
Patients who do not agree to participate in the study.
Patients who, in addition to surgery, have other serious medical problems (ASA III-VI) or suffer from psychotic disorders or drug addiction.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Midline laparotomy surgery site pain. Timepoint: Before beginning of the intervention, 24, 48, 72 hour's after beginning of the intervention. Method of measurement: visual analogue scale.;Local complications of the laparotomy site. Timepoint: Before beginning of the intervention, 24, 48, 72 hour's after beginning of the intervention. Method of measurement: Inspection of the operation site.;Serum Inflammatory factors. Timepoint: Before beginning of the intervention, 24, 48, 72 hour's after beginning of the intervention. Method of measurement: Taking daily blood tests.
- Secondary Outcome Measures
Name Time Method The amount of painkillers. Timepoint: Before beginning of the intervention, 24, 48, 72 hour's after the start of the intervention. Method of measurement: check the patient's medical record.