Postoperative pain control by topical subcutaneous analgesic injection at the end of surgery
Phase 3
Recruiting
- Conditions
- Pain control after surgery for ovarian malignancies.Malignant neoplasm of ovary
- Registration Number
- IRCT20220108053667N1
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
Patients aged 40-60 years
BMI = 25-30
without previous history of laparotomy
ovarian mass with ultrasound, CT scan (solid cystic masses, papillary projection, abdominal ascites, parietal nodules, etc.) and tumor marker based on malignancy ( High levels of markers CA125 and CEA)
laparotomy with midline incision
average operation time of 60 to 90 minutes
Exclusion Criteria
History of severe heart disease
anemia
liver disease
kidney disease
anesthetic allergy
history of hypotension or hypertension
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain score of patients after surgery. Timepoint: 2, 6, 12 and 24 hours after surgery. Method of measurement: Patients' pain is measured based on Visual Analog Scale.
- Secondary Outcome Measures
Name Time Method Recurrence of intestinal function. Timepoint: 12 and 24 hours after surgery. Method of measurement: Questions from the patient and patient file information.;Opioid use to control pain. Timepoint: 2,6,12,24 hours post operation. Method of measurement: patient file information.;Diclofenac suppository and acetaminophen injection for pain control. Timepoint: 2,6,12,24 hours post operation. Method of measurement: patient file information.