NCT02207855CompletedNot Applicable
Chloroprocaine for Continuous Epidural Analgesia in Neonates and Infants
Joseph D. Tobias1 site in 1 country21 target enrollmentStarted: June 2014Last updated:
Conditions
Interventions
Drugs
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 21
- Locations
- 1
- Primary Endpoint
- Pain score
Study Overview
Brief 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.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Retrospective
Eligibility Criteria
- Ages
- — to 2 Years (Child)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Neonates and infants who have received chloroprocaine for epidural anesthesia.
Exclusion Criteria
- Not provided
Arms & Interventions
Chloroprocaine
Neonates and infants who have received chloroprocaine for epidural anesthesia.
Intervention: Chloroprocaine (Drug)
Outcomes
Primary Outcomes
Pain score
Time Frame: Every 6 hours for 72 hours
Secondary Outcomes
- Pain medicine consumption(Every 6 hours for 72 hours)
Investigators
Joseph D. Tobias
Chairman, Dept. of Anesthesiology & Pain Medicine
Nationwide Children's Hospital
Study Sites (1)
Loading locations...
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