To determine the efficacy and safety of oxycodone i.v. patient-controlled analgesia (PCA) in the pain relieving treatment during 48h postoperative period, by comparing with morphine i.v. PCA.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
240
Investigational site
Beijing, Beijing Municipality, China
Measuring VAS
Measuring resting and coughing VAS, assessing the intensity of pain
Time frame: 3h post-operation
Measuring VAS
Measuring resting and coughing VAS, assessing the intensity of pain
Time frame: 24 hours post operation
Measuring VAS
Measuring resting and coughing VAS, assessing the intensity of pain
Time frame: 48 hours post operation
Dosage
Total dosage of study drugs within 48h.
Time frame: Within 48h
The dosage of other rescue analgesic drugs used within 48h post-operation.
The dosage of other rescue analgesic drugs used within 48h post-operation.
Time frame: 48hrs
The invalid times and the total times of PCA application
The invalid times and the total times of PCA application
Time frame: 48hrs
Satisfaction degree for analgesia
Satisfaction degree for analgesia after the treatment
Time frame: 48hrs
AE occurrence and abnormal lab value
AE and normal lab value will be recorded during the study
Time frame: 48hrs
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