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NCT03307590 Clinical Trial

Comparing Dexmedetomidine With Bupivacaine Versus Bupivacaine Alone for Caudal Block in Supra - Umbilical Surgeries

Anesthesia Clinical Trial

Official title:
Adding Dexmedetomidine to Caudal Bupivacaine for Analgesia in Supra - Umbilical Pediatric Surgeries: Would it Add More Analgesia

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03307590
Other study ID # Caudaldexsupraumblical
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received
Last updated
Start date October 1, 2017
Est. completion date December 30, 2017

Study information
Verified date July 2018
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

dexmedetomidine is an alpha 2 adrenergic receptor agonist that is given either systemically or combined to local anesthetics during regional blocks. Investigators studied the combination of dexmedetomedine/bupivacaine versus bupivacaine alone for caudal blockage in pediatric patients undergoing supra - umbilical surgeries.

Description:

Dexmedetomidine was combined to bupivavaine and administered via caudal route to be compared to caudal bupivavaine alone for analgesia following upper trunk surgery

Recruitment information / eligibility
Status Completed
Enrollment 24
Est. completion date December 30, 2017
Est. primary completion date December 30, 2017
Accepts healthy volunteers No
Gender All
Age group 1 Year to 6 Years
Eligibility Inclusion Criteria:

- supra - umbilical surgeries

Exclusion Criteria:

- allergy to the drug or coagulopathy

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Dexmedetomidine
Caudal block by dexmedetomidine and bupivavaine
• Bupivacaine
Caudal block by bupivavaine alone

Locations
Country Name City State
Egypt Cairo University Cairo

Sponsors (1)
Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain relief CHEOPS scale value 6 months study
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