Overview

Efficacy and Safety of Single, Low-dose Dexamethasone in Patients After Total Knee Arthroplasty

Status:
Completed
Trial end date:
2012-01-01
Target enrollment:
0
Participant gender:
All
Summary
This study was conducted to determine the efficacy of an additional preemptive, single, low-dose dexamethasone in terms of incidence and severity of postoperative nausea/vomiting (PONV), pain level, and the safety in terms of wound complications in patients managed with our antiemetic protocol based on Ramosetron following TKA.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Tae Kyun Kim
Treatments:
BB 1101
Dexamethasone
Dexamethasone 21-phosphate
Dexamethasone acetate
Criteria
Inclusion Criteria:

- Diagnosis of primary osteoarthritis, knee

- Scheduled for elective total knee arthroplasty

- Signed written informed consent

Exclusion Criteria:

- Refusing participate

- Contraindication to regional anesthesia

- Severe impairment of bowel motility

- administration of other antiemetic drug within 24hours before surgery

- systemic steroid within 24hours before surgery

- history of cardiovascular & respiratory disease

- renal & hepatic failure