Effect of ropivacaine with ketamine for post-tonsillectomy pain control in pediatric patient

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0001781

Enrollment

Registered

2016-01-26

Start date

2015-12-28

Completion date

Unknown

Last updated

2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Drug : After surgery is over, topical soaking of drugs on both tonsillar bed with guaze packing for 5 minute and awake patient from general anesthesia. Control group : 0.75% ropivacaine 5cc with salin

Eligibility

Sex/Gender

All

Inclusion criteria

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

Exclusion criteria: 1. Refuse of patient's parent. 2. Patients with cardiac abnormalities. 3. Patients with allergic history of ropivacaine or ketamine.

Design outcomes

Primary

Measure	Time frame
modified Children's Hospital of Eastern Ontario Pain Scale (mCHEOPS)	—

Secondary

Measure	Time frame
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	—

Countries

Korea, Republic of

Contacts

Public ContactBoohwi Hong

Chungnam National University Hospital

koho0127@gmail.com+82-42-280-7840

Outcome results