Status:
COMPLETED
Intravenous Paracetamol for Postoperative Pain
Lead Sponsor:
Lithuanian University of Health Sciences
Conditions:
Pain, Postoperative
Recovery of Function
Eligibility:
All Genders
1-18 years
Phase:
PHASE4
Brief Summary
The purpose of this study is to define if intravenous paracetamol may improve analgesia and outcome in pediatric surgical patients treated with non-steroidal anti-inflammatory drugs (NSAIDs) postopera...
Detailed Description
Patients aged 1-18 years undergoing general, plastic or orthopedic surgery with expected moderate to severe pain at least for 24 hours postoperatively, who meet inclusion criteria and does not meet ex...
Eligibility Criteria
Inclusion
- Patients 1-18 years of age, undergoing general, plastic or orthopedic surgery with expected median to severe pain postoperatively.
- physical status of the patient corresponding to American Society of Anesthesiologists (ASA) class 1 or 2
- Signed written informed consent by parents/official caregivers.
Exclusion
- Allergy to paracetamol, ketoprofen, tramadol, morphine or any NSAID
- oncologic disease
- central nervous system disease
- renal dysfunction
- hepatic dysfunction
- bronchial asthma
- ulcer(s) in gastrointestinal system
- hemorrhagic diathesis
- chronic use of NSAIDs
- chronic use of opioids
- chronic use of anticoagulants
- female patient is known to be pregnant
Key Trial Info
Start Date :
November 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2017
Estimated Enrollment :
54 Patients enrolled
Trial Details
Trial ID
NCT02248493
Start Date
November 1 2012
End Date
March 1 2017
Last Update
March 6 2017
Active Locations (1)
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1
Lithuanian University of Health Sciences Kaunas Clinics
Kaunas, Lithuania, 50009