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Clinical Trials/EUCTR2010-018600-87-IT
EUCTR2010-018600-87-IT
Active, not recruiting
Not Applicable

POST-OPERATIVE PAIN CONTROL OF PEDIATRIC PATIENTS UNDERWENT ORTHOPEDIC SURGERY: COMPARISON OF INTRAVENOUS ANALGESIA AND ONE-SHOT EPIDURAL LUMBAR NERVE BLOCK. - Peri-Trauma

AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA0 sitesMarch 1, 2010
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ConditionsPOST-OPERATIVE PAIN CONTROL OF PEDIATRIC PATIENTS UNDERWENT ORTHOPEDIC SURGERYMedDRA version: 9.1Level: SOCClassification code 10028395
DrugsNAROPINACATAPRESANTORADOLCONTRAMALPERFALGAN

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
POST-OPERATIVE PAIN CONTROL OF PEDIATRIC PATIENTS UNDERWENT ORTHOPEDIC SURGERY
Sponsor
AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA
Status
Active, not recruiting
Last Updated
14 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 1, 2010
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA

Eligibility Criteria

Inclusion Criteria

  • •\- child aged between 6 and 13 years \- ASA 1\-2 \- interventions for correction of splayfoot (sec. Castmann) and genu valgum or varum deformities (eight\-plate)
  • •Are the trial subjects under 18? yes
  • •Number of subjects for this age range:
  • •F.1\.2 Adults (18\-64 years) no
  • •F.1\.2\.1 Number of subjects for this age range
  • •F.1\.3 Elderly (\>\=65 years) no
  • •F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • •\- age less than 6 and more than 13 years \- ASA 3\-4 \- lack of patient or his/her parents accordance \- positive history for asthma or other cardio\-respiratory disease \- allergy of local anesthetics or propofol \- central nervous system or psychiatric disorders \- coagulopathy or bleeding diathesis \- undergoing infection with systemic manifestation \- failure of loco\-regional nerve block

Outcomes

Primary Outcomes

Not specified

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