Lumbar Infiltration With Steroids - Effects on Pain Reduction
1 other identifier
observational
60
1 country
1
Brief Summary
Questionnaire for patients who got a lumbar infiltration in our clinic. The patients will have to answer questions concerning their pain. (The lumbar infiltration itself is not part of this study)
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Dec 2010
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2010
CompletedFirst Submitted
Initial submission to the registry
April 5, 2011
CompletedFirst Posted
Study publicly available on registry
April 7, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2013
CompletedJune 3, 2015
May 1, 2015
3 years
April 5, 2011
June 2, 2015
Conditions
Outcome Measures
Primary Outcomes (1)
Pain reduction
on visual analog scale
week 1 and 3; month 3, 6, 12
Interventions
no intervention. Only questionnaire after lumbar infiltration with steroids - effects on pain reduction
Eligibility Criteria
Patients who got a lumbar infiltration in our clinic. The patients will have to answer questions concerning their pain (the lumbar infiltration itself is not part of this study).
You may qualify if:
- Patients who got a lumbar infiltration in our clinic.
You may not qualify if:
- Infiltration of thoracal or cervical spine.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University Hospital Zurich, Division of Rheumatology
Zurich, Switzerland
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Sandra Blumhardt, MD
University Hospital Zurich, Division of Rheumatology
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 5, 2011
First Posted
April 7, 2011
Study Start
December 1, 2010
Primary Completion
December 1, 2013
Study Completion
December 1, 2013
Last Updated
June 3, 2015
Record last verified: 2015-05