Study on spinal anestesiology whitbupivacaine, levobupivacaine e ropivacaine. - ND

• Conditions: Spinal anestesiology for perianal surgery; MedDRA version: 9.1Level: HLTClassification code 10002580Term: Anorectal therapeutic procedures

• Registration Number: EUCTR2009-010807-10-IT
• Lead Sponsor: AZIENDA OSPEDALIERA DI PADOVA

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2009-05-22
• Last Update Posted: 19 March 2012

Recruitment & Eligibility

• Status: Authorised-recruitment may be ongoing or finished
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

both sex,
18< age< 80 years old
ASA class I, II o III.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Heart failure(NYHA III-IV), liver and renal failure, psichiatric disorders

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Main Objective: Evalutation of bupivacaine, levobupivacaine e ropivacaine for intratecal use in perianal surgery.;Secondary Objective: ;Primary end point(s): Block efficacy