Nationwide Children's Hospital
Columbus, Ohio, 43205, United States
Completed
NCT Number: NCT01930201
Caudal Epidural Block for Postoperative Analgesia in Adolescents Following Major Hip Surgery.
This retrospective chart review will demonstrate the feasibility of performing caudal epidural blockade in adolescents undergoing major orthopedic hip surgery and provide information regarding the feasibility of this technique's use on a regular basis.
Completed
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Notify MeKey information
Conditions
Sex eligibility
All sexes
Study type
Observational
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Adolescents that underwent major orthopedic hip surgery.
Exclusion criteria
- None.
Treatment and study plan
Caudal Epidural Block
ProcedureGeneral anesthesia
OtherPrimary outcomes
-
Pain
Time frame: During 1st 24 hours post-op
Assessing pain scores post-operatively.
Secondary outcomes
-
Pain medication requirement
Time frame: During 1st 24 hours post-op
Assessing amount of pain medication required.
-
Antiemetic medication requirement
Time frame: During 1st 24 hours post-op
Assessing need for antiemetic medications post-operatively.
Sponsors and collaborators
Lead sponsor
David P. Martin
Other
Registry information
Important dates
- Study start
- 2013
- Primary completion
- 2013
- Study completion
- 2013
- First posted
- Aug 28, 2013
- Registry last updated
- Oct 29, 2014
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.