Effect of ropivacaine with ketamine for post-tonsillectomy pain control in pediatric patient
Not Applicable
Completed
- Conditions
- Diseases of th respiratory system
- Registration Number
- KCT0001781
- Lead Sponsor
- Chungnam National University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
1. 3 years to 7 years patients who are scheduled to have elective tonsillectomy or tonsillectomy and adenoidectomy.
2. American Society of Anesthesiologist(ASA) Class I and II patients
Exclusion Criteria
1. Refuse of patient's parent.
2. Patients with cardiac abnormalities.
3. Patients with allergic history of ropivacaine or ketamine.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method modified Children's Hospital of Eastern Ontario Pain Scale (mCHEOPS)
- Secondary Outcome Measures
Name Time Method Amount of administered analgesics for 24 hours;First request time of analgecis;Postoperative modified Children's Hospital of Eastern Ontario Pain Scale(mCHEOPS) score at 15 minute, 30 minute, 2 hours, 4 hours, 6 hours, 8 hours, 16 hours, 24 hours