Status:

COMPLETED

Comparison of Active vs. Passive Surveillance to Collect Adverse Events

Lead Sponsor:

University of Alberta

Conditions:

Adverse Events

Eligibility:

All Genders

Phase:

NA

Brief Summary

This cluster randomized trial will be the first to specifically evaluate passive versus active surveillance methods collection of adverse events (AEs). The evaluation of these methods will be performe...

Eligibility Criteria

Inclusion

  • Licensed doctors of chiropractic who provide manual therapy in US or Canada
  • Willing to collect data per protocol for 60 consecutive pediatric (13 years of age and younger) patients

Exclusion

  • \- Doctors of chiropractic and patient participation will be limited to those that speak / read English.

Key Trial Info

Start Date :

October 1 2014

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

July 1 2017

Estimated Enrollment :

96 Patients enrolled

Trial Details

Trial ID

NCT02268331

Start Date

October 1 2014

End Date

July 1 2017

Last Update

October 25 2017

Active Locations (1)

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CARE

Edmonton, Alberta, Canada, T5K 0L4