Comparison of diclofenac and acetaminophen in the managment of pain after back surgery.

Not Applicable

Completed

• Conditions: acute postoperative pain.; Acute pain; R52.0A

• Registration Number: IRCT201311168768N3
• Lead Sponsor: Vice chancellor for Research and Technology, Hamadan University Of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

inclusion criteria: Patients candidate for laminectomy with American Society of Anesthesiologists ( ASA ) class I, II
Exclusion criteria: Patients with Coagulation disorders, seizure, Asthma, renal or hepatic disease, addiction to opioids or alchohol, sensitivity to NSAIDS or acetaminophen, peptic ulcer disease, opium or NSAIDs use in recent 24 hr, surgery time more than 150 minutes and patient refusal

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain score. Timepoint: In recovery, 6 hours after surgery, 12 hours after surgery, 24 hours after surgery. Method of measurement: Visual Analogue Scale.;Total dose of narcotic used in patient controlled analgesia. Timepoint: 24 hours after surgery. Method of measurement: Observation of PCA pomp and calculating the used narcotic by microgram.;Patient satisfaction. Timepoint: 24 hours after surgery. Method of measurement: Questionare.;Total dose of Adjuvant analgesic. Timepoint: 24 hours after surgery. Method of measurement: With questionare and by miligram.

Secondary Outcome Measures

Name	Time	Method
ausea and vomiting. Timepoint: In recovery, 6 hours after surgery, 12 hours after surgery, 24 hours after surgery. Method of measurement: Questionare.;Sedation score. Timepoint: At the end of the surgery, after 24 hours. Method of measurement: By using Ramsy sedation scale.