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Guideline ImplementationNCT00372164

Retrospective Evaluation of ASIPP Guidelines Implementation

An observational study of Guideline Implementation, run by Pain Management Center of Paducah at 1 site in United States.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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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. Read more about this study

Who is it for?
Any age
Conditions the study is for
Guideline Implementation
What is being tested?
American Society of Interventional Pain Physician Guidelines
Type of treatment
Surgery or procedure
How many people
0 participants
Where
1 siteUnited States
Study dates
Jan 1998to Jul 2005
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: current patients

Who may be able to join

  • 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

Who cannot join

  • Non-availability of appropriate data

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Ambulatory Surgery Center

    Paducah, Kentucky, 42001

Other trials in United States

About this study

Official title: Evaluation of the Effectiveness of Implementation of American Society of Interventional Pain Physician Guidelines for Interventional Techniques: A Retrospective Evaluation

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.

Read the detailed 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.

Being tested
American Society of Interventional Pain Physician Guidelines
Keywords
ASIPP, Guidelines

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • American Society of Interventional Pain Physician GuidelinesProcedure or surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Sep 2006 (estimated)
  2. Study startJan 1998
  3. Study completionJul 2005

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Retrospective
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00372164
Sponsor's protocol ID
protocol 14
Status last verified
Oct 2015
First submitted
1 Sep 2006
Last updated
21 Oct 2015
Results posted
No

Questions about this trial

What is this clinical trial studying?

An observational study of Guideline Implementation, run by Pain Management Center of Paducah at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: withdrawn, as of the sponsor's last update on 21 Oct 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Oct 2015.

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