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Complications and Adverse Effects in Continuous Peripheral Regional Anesthesia

NCT00251654 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 9000

Last updated 2009-10-01

No results posted yet for this study

Summary

The investigators prospectively document infectious, neurological, and other complications or adverse events occurring during peripheral regional anesthesia via a catheter using computer-based data recording.

Conditions

Interventions

PROCEDURE

perineural block (anesthesia)

continuous peripheral regional anesthesia ropivacaine 0.33% for 3 to 5 days

Sponsors & Collaborators

  • BG Unfallklinik Murnau

    collaborator OTHER

  • Rechbergklinik Bretten

    lead OTHER

Principal Investigators

  • Johannes Büttner, MD · BG Unfallklinik Murnau

Eligibility

Min Age
1 Year
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2002-01-31
Primary Completion
2008-12-31
Completion
2008-12-31

Countries

  • Germany

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00251654 on ClinicalTrials.gov