Skip to main content
OpenTrials
Completed

NCT Number: NCT01494272

Analgesia in Children Using Caudal Epidural Ropivacaine

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

Completed

Looking for future studies?

Notify Me

Key information

Age range

2 month–2 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Loma Linda University Medical Center, Loma Linda, California, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • Contraindications to caudal epidural analgesia
  • parent's refusal
  • skeletal or spinal cord anomaly
  • coagulopathy
  • infection at the insertion site
  • ongoing bacteremia
  • allergy to ropivacaine

Treatment and study plan

Primary outcomes

  1. Usage of pain medications

    Time frame: over 24 hours

Secondary outcomes

  1. Pain scores

    Time frame: At various intervals for first 24 hours

Sponsors and collaborators

Lead sponsor

Loma Linda University

Other

Registry information

Official study title

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

Important dates

Study start
2012
Primary completion
2014
Study completion
2015
First posted
Dec 16, 2011
Registry last updated
Nov 25, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.