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Clinical Trials/DRKS00005059
DRKS00005059
Completed
未知

A quantitative analysis of sedation in infants with caudal blockade - /

Anästhesie, Allgemeine Intensivmedizin und Schmerztherapie0 sites34 target enrollmentJune 1, 2015
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ConditionsK40.9Unilateral or unspecified inguinal hernia, without obstruction or gangrene

Overview

Phase
未知
Intervention
Not specified
Conditions
K40.9
Sponsor
Anästhesie, Allgemeine Intensivmedizin und Schmerztherapie
Enrollment
34
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 1, 2015
End Date
October 7, 2015
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Anästhesie, Allgemeine Intensivmedizin und Schmerztherapie

Eligibility Criteria

Inclusion Criteria

  • •Infants aged between 0 and 3 months
  • •\- Lower body surgery with planned caudal blockade
  • •\- Written informed consent given by parents after being provided with detailed information about the nature, risks, and scope of the clinical study

Exclusion Criteria

  • •\- Parents refusal
  • •\- Contraindications against a caudal blockade
  • •\- Coagulopathy

Outcomes

Primary Outcomes

Not specified

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