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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01330875
Other study ID # LINFRUZ01
Secondary ID
Status Completed
Phase N/A
First received April 5, 2011
Last updated June 2, 2015
Start date December 2010
Est. completion date December 2013

Study information

Verified date May 2015
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Observational

Clinical Trial 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)


Description:

Questionnaire are given to patients who got a lumbar infiltration in our clinic of rheumatology. These patients will have to answer questions concerning their pain. (The lumbar infiltration itself is not part of this study).


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date December 2013
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion criteria:

- Patients who got a lumbar infiltration in our clinic.

Exclusion criteria:

- Infiltration of thoracal or cervical spine.

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
survey
no intervention. Only questionnaire after lumbar infiltration with steroids - effects on pain reduction

Locations

Country Name City State
Switzerland University Hospital Zurich, Division of Rheumatology Zurich

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain reduction on visual analog scale week 1 and 3; month 3, 6, 12 No
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