postoperative pain
Conditions
Interventions
1:Betamethasone combined with Ropivacain
2:Dexamethasone combined with Ropivacain
3:Ropivacain
Sponsors
The Second Xiangya Hospital, Central South University
Eligibility
Sex/Gender
All
Age
14 Years to 65 Years
Inclusion criteria
Inclusion criteria: Patient who agree with Regional and General Anesthesia for surgery; ASA grade I to II; ablity to comprehend visual analogue scale (VAS) pain scoring system or use patient controlled analgesia (PCA) pump.
Exclusion criteria
Exclusion criteria: Any clinically relevant abnormal physical findings; History of anaphylaxis to drugs or allergic reactions in general, which the investigator considers may affect the outcome of the study; Relevant history of renal, cardiovascular, respiratory, gastrointestinal, musculoskeletal, skin (particularly at the site of drug application), haematological, endocrine or neurological diseases that may interfere with the aim of the study; Using other medications which interfere with the IMP of the study during 1 week before the start of IMP.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| postoperative pain reduction on VAS;analgesic consumption;time of the first patient-controlled intravenous analgesia;recovery quality; | — |
Countries
China
Contacts
Public ContactXu Junmei
Central South University
Outcome results
None listed