Ignite Creation Date:
2024-05-05 @ 5:24 PM
Last Modification Date:
2024-10-26 @ 9:31 AM
Study NCT ID:
NCT00445016
Status:
UNKNOWN
Last Update Posted:
2008-05-09
First Post:
2007-03-07
Brief Title:
Neurologic Complications in Peripheral Regional Anesthesia - An Evaluation Based on a Standardized Protocol
Sponsor:
BG Unfallklinik
Organization:
BG Unfallklinik
Study Overview
Official Title:
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
Status:
UNKNOWN
Status Verified Date:
2008-05
Last Known Status:
ACTIVE_NOT_RECRUITING
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
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
Detailed Description:
Neurologic complications as an adverse effect occur in all types of regional anesthesia Reviewing the literature the incidence spreads from 002 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
The patients will be recruited among all patients from our hospital receiving continuous peripheral regional anesthesia
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None