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Neurologic Complications in Peripheral Regional Anesthesia - An Evaluation Based on a Standardized Protocol

The recruitment status of this study is unknown because the information has not been verified recently.
Verified May 2008 by BG Unfallklinik.
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by:
BG Unfallklinik
ClinicalTrials.gov Identifier:
NCT00445016
First received: March 7, 2007
Last updated: May 5, 2008
Last verified: May 2008

March 7, 2007
May 5, 2008
May 2008
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Complete list of historical versions of study NCT00445016 on ClinicalTrials.gov Archive Site
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Neurologic Complications in Peripheral Regional Anesthesia - An Evaluation Based on a Standardized Protocol
Neurologic Complications in Peripheral Regional Anesthesia - A Clinical Follow Up Study to Evaluate the Incidence of Neurologic Complications Defined According to a Standardized Protocol Considering Motoric and Sensory Function and Pain

To evaluate the incidence of neurologic complications as a consequence of peripheral regional anesthesia, all patients receiving peripheral nerve blocks will be evaluated according to a standardized protocol screening pain, motoric and sensory function recovering to defined periods, and according to a study protocol defining the items.

Neurologic complications as an adverse effect occur in all types of regional anesthesia. Reviewing the literature, the incidence spreads from 0.02 up to 3 percent. The incidence remains unclear because of different types of definitions, too. In this study, we evaluate all patients receiving peripheral regional anesthesia 24 hours after block performance according to a standardized study protocol. In case of any conspicuousness concerning motoric or sensory function or pain, the patient will be evaluated again after 48 hours. Further on, in case of neurologic dysfunction, periods of investigation will be after 3 days, 1 week, 2 weeks, 1 month, 3 months, 6 months and 1 year. This study includes the definition for nerve damage concerning motoric and sensory neural function and pain.

The patients will be recruited among all patients from our hospital receiving continuous peripheral regional anesthesia.

Observational
Time Perspective: Prospective
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Non-Probability Sample

Patients receiving peripheral regional anesthesia (routine)

  • Anesthesia, Conduction
  • Nerve Block
  • Adverse Effects
Procedure: peripheral regional anesthesia
evaluation and description of adverse effects
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
1000
December 2008
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Inclusion Criteria:

  • All patients receiving peripheral regional anesthesia

Exclusion Criteria:

  • Missing agreement
Both
10 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
Germany
 
NCT00445016
nd001
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Dr Michael Neuburger, BG Unfallklinik Murnau
BG Unfallklinik
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Study Chair: Johannes Buettner, MD BG Unfallklinik Murnau
BG Unfallklinik
May 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP