NCT00445016

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
1,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2008

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 7, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

March 8, 2007

Completed
1.2 years until next milestone

Study Start

First participant enrolled

May 1, 2008

Completed
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2008

Completed
Last Updated

May 9, 2008

Status Verified

May 1, 2008

First QC Date

March 7, 2007

Last Update Submit

May 5, 2008

Conditions

Keywords

peripheral regional anesthesianerve damageadverse effectsneurologic complicationneuropathy

Interventions

evaluation and description of adverse effects

Eligibility Criteria

Age10 Years+
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients receiving peripheral regional anesthesia (routine)

You may qualify if:

  • All patients receiving peripheral regional anesthesia

You may not qualify if:

  • Missing agreement

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

BG Unfallklinik

Murnau am Staffelsee, Bavaria, 82418, Germany

Location

Related Links

Study Officials

  • Johannes Buettner, MD

    BG Unfallklinik Murnau

    STUDY CHAIR

Study Design

Study Type
observational
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

March 7, 2007

First Posted

March 8, 2007

Study Start

May 1, 2008

Study Completion

December 1, 2008

Last Updated

May 9, 2008

Record last verified: 2008-05

Locations