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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00372164
Other study ID # protocol 14
Secondary ID
Status Withdrawn
Phase N/A
First received September 1, 2006
Last updated October 20, 2015
Start date January 1998
Est. completion date July 2005

Study information

Verified date October 2015
Source Pain Management Center of Paducah
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

To demonstrate clinically significant improvements in the patients treated following ASIPP guidelines compared to the patients who were treated prior to the establishment of ASIPP guidelines.


Description:

We have performed one study in the past showing that the implementation of guidelines improved outcomes by reducing the number of procedures and also the cost. However,, no large scale study has been performed thus far.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date July 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

Evaluate all patients undergoing the following interventional techniques during 1999 and 2000 compared to patients undergoing interventional techniques during 2004 and 2005

- Cervical facet joint nerve blocks

- Thoracic facet joint nerve blocks

- Lumbar facet joint nerve blocks

- Lumbar interlaminar epidural steroid injections

- Cervical interlaminar epidural steroid injections

Exclusion Criteria:

Non-availability of appropriate data

Study Design

Observational Model: Case Control, Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Procedure:
American Society of Interventional Pain Physician Guidelines


Locations

Country Name City State
United States Ambulatory Surgery Center Paducah Kentucky

Sponsors (1)

Lead Sponsor Collaborator
Pain Management Center of Paducah

Country where clinical trial is conducted

United States,