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NCT02207855 Clinical Trial

Chloroprocaine for Continuous Epidural Analgesia in Neonates and Infants

Anesthesia Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02207855
Other study ID # IRB14-00231
Secondary ID
Status Completed
Phase N/A
First received August 1, 2014
Last updated November 28, 2016
Start date June 2014
Est. completion date March 2015

Study information
Verified date November 2016
Source Nationwide Children's Hospital
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

This a study to retrospectively review our experience with the use of chloroprocaine for postoperative epidural infusions in neonates and infants. Pain scores and the need for intravenous analgesic agents will be recorded from the records to demonstrate the efficacy of the technique.

Recruitment information / eligibility
Status Completed
Enrollment 21
Est. completion date March 2015
Est. primary completion date March 2015
Accepts healthy volunteers No
Gender Both
Age group N/A to 2 Years
Eligibility Inclusion Criteria:

- Neonates and infants who have received chloroprocaine for epidural anesthesia.

Exclusion Criteria:

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

Intervention

Drug:
• Chloroprocaine

Locations
Country Name City State
United States Nationwide Children's Hospital Columbus Ohio

Sponsors (1)
Lead Sponsor Collaborator
Joseph D. Tobias

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain score Every 6 hours for 72 hours No
Secondary Pain medicine consumption Every 6 hours for 72 hours No
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