The Effects of Single-dose Rectal Midazolam Application on Post-operative Recovery

PHASE4CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

June 30, 2005

Primary Completion Date

June 30, 2006

Study Completion Date

June 30, 2006

Conditions
Failed Moderate Sedation During Procedure
Interventions
DRUG

1 mL/kg bupivacaine 0.25%.

40 children between 2 and 10 years of ASA I-II were randomized and they received caudal anesthesia under general anesthesia. Patients underwent the application of caudal block in addition with saline and 1 mL/kg bupivacaine 0.25%. In the postoperative period, Group C (n=20) was given 5mL saline and Group M (n=20) was given 0.30 mg/kg rectal midazolam diluted with 5mL saline. Sedation scale and postoperative pain scale (CHIPPS) of the patients were evaluated. The patients were observed for their analgesic need, first analgesic time, and adverse effects for 24 hours.

Trial Locations (1)

61080

Karadeniz Technical University Faculty of Medicine, Trabzon

All Listed Sponsors
lead

Karadeniz Technical University

OTHER

NCT02127489 - The Effects of Single-dose Rectal Midazolam Application on Post-operative Recovery | Biotech Hunter | Biotech Hunter