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OpenTrials
Completed

NCT Number: NCT01330875

Lumbar Infiltration With Steroids - Effects on Pain Reduction

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)

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Key information

Conditions

Low Back Pain Back Pain Neurologic Manifestations Pain Pathological Conditions, Signs and Symptoms Signs and Symptoms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital Zurich, Division of Rheumatology

Zurich, Switzerland

About this study

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).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients who got a lumbar infiltration in our clinic.

Exclusion criteria

  • Infiltration of thoracal or cervical spine.

Treatment and study plan

Survey

Other

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

Primary outcomes

  1. Pain reduction

    Time frame: week 1 and 3; month 3, 6, 12

    on visual analog scale

Sponsors and collaborators

Lead sponsor

University of Zurich

Other

Registry information

Important dates

Study start
2010
Primary completion
2013
Study completion
2013
First posted
Apr 7, 2011
Registry last updated
Jun 3, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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