Change in pain after laparoscopy.
Conditions
Interventions
Intervention 1: The patients in group 1 will receive Paracetamol 1 g IV and normal saline intraperitoneal, 10 minutes before the end of operation. Intervention 2: Group 2 will receive normal saline I
Treatment - Drugs
The patients in group 1 will receive Paracetamol 1 g IV and normal saline intraperitoneal, 10 minutes before the end of operation
Group 2 will receive normal saline IV and intraperitoneal bupivacaine 0.25%, 40ml –pethidine 50 mg, 10 minutes before the end of operation.
Sponsors
Tabriz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 38 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria:Women with 20-38 years old; candidated for gynecologic diagnostic Laparoscopy; patients with ASA physical status I and II; patients who will give written informed consent Exclusion criteria: Women with ASA physical status III or higher;patients who received analgesic; patients who had contraindication for NSAIDs or Paracetamol like peptic ulcer; coagulopathy; renal failure;hepatic failure; allergy
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative pain. Timepoint: 2, 4, 6, 8, 12, 24 hours postoperative. Method of measurement: with the use of visual Analogue Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Sedation. Timepoint: 2, 4, 6, 8, 12, 24 hours post operative. Method of measurement: with the use of modified Ramssy sedation scoring. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr.Sousan Rasooli
Alzahra Hospital
Outcome results
None listed