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Analgesia in Children Using Caudal Epidural Ropivacaine

Preemptive Analgesia in Children Using Caudal Epidural Ropivacaine: A Prospective, Randomized, Double-blinded, Controlled Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01494272
Enrollment
90
Registered
2011-12-16
Start date
2012-06-30
Completion date
2015-05-31
Last updated
2015-11-25

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

Conditions

Circumcision, Inguinal Hernia

Keywords

caudal epidural analgesia, elective circumcision, elective inguinal herniorrhaphy

Brief summary

Caudal epidural analgesia (caudal block)is used in standard pediatric anesthesia practice. It has been shown to be effective in managing postoperative pain in children undergoing abdominal and infraumbilical surgery (Tobias et al 1994). Furthermore, studies have shown that children receiving caudal blocks have secondary benefits such as lower narcotic and anesthetic requirements, more rapid awakening from general anesthesia, decreased time to discharge home, and fewer pain-related behaviors postoperatively (Conroy et al 1993, Tobias et al 1995, Tobias 1996). This proposed study involves the use of a caudal block in children undergoing elective inguinal herniorrhaphy or orchiopexy to evaluate the role of preemptive analgesia in pediatric pain management. We hypothesize that by inhibiting peripheral pain receptors with a caudal block before the onset of a painful stimulus, we can decrease central nervous system sensitization and reduce postoperative analgesic requirements

Interventions

None listed

Sponsors

Loma Linda University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
2 Months to 2 Years
Healthy volunteers
Yes

Inclusion criteria

1. Age 2 months to 2 years 2. Weight 25kg or less 3. ASA class 1, 2, 3 4. Elective inguinal herniorrhaphy or orchiopexy

Exclusion criteria

1. Contraindications to caudal epidural analgesia 2. parent's refusal 3. skeletal or spinal cord anomaly 4. coagulopathy 5. infection at the insertion site 6. ongoing bacteremia 7. allergy to ropivacaine

Design outcomes

Primary

MeasureTime frame
Usage of pain medicationsover 24 hours

Secondary

MeasureTime frame
Pain scoresAt various intervals for first 24 hours

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026