Status:
COMPLETED
Duloxetine and Dexamethasone for Improving Postoperative Pain
Lead Sponsor:
Ain Shams University
Conditions:
Post Operative Pain Control
Eligibility:
FEMALE
25-35 years
Phase:
PHASE4
Brief Summary
75 female patients were randomly allocated into one of three equal groups. Group I(GI) received Dulox 60 mg orally and 100 ml 0.9% sodium chloride solution (NS) intravenous infusion (IVI) over 15 min,...
Detailed Description
This study was designed to be a randomized, placebo-controlled, double-blinded parallel study and this study was carried out at Ain-Shams university hospitals, from December 2014 to January2016, on 75...
Eligibility Criteria
Inclusion
- female patients aged between 25 and 35 years old of the American Society of Anesthesiologists (ASA) physical status I and II scheduled for elective laparoscopic gynecological surgeries (for infertility) under general anesthesia.
Exclusion
- patient's refusal,
- duration of surgery more than 90 minutes,
- allergy to any drugs of the study,
- smokers, history of drug or alcohol abuse,
- treatment with antidepressants,
- history of diabetes or epilepsy,
- , history of chronic pain or daily intake of analgesics within 24 h before surgery,
- treatment with systemic glucocorticoids within 4 weeks before surgery and (9) impaired kidney or liver functions. -
Key Trial Info
Start Date :
December 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2016
Estimated Enrollment :
75 Patients enrolled
Trial Details
Trial ID
NCT03250494
Start Date
December 1 2014
End Date
January 1 2016
Last Update
August 15 2017
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