The purpose of this study is to determine whether experimentally induced acute low back pain
might lead to alteration in lumbar tactile acuity measured in region affected by pain
compared to pain-free side and pain-free controls.
Other: Saline injection
Other: Sham injection
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Full eligibility criteria for NCT03021278
Ages eligible for Study
18 Years to 35 Years
Genders eligible for Study
Accepts Healthy Volunteers
Only participants with similar mechanical detection threshold (MDT) on both sides of the spine will be included.
age < 18 or > 35 years
current pain experience
episodes of back pain lasting more than 24 hours within the previous one-month period
history of chronic pain, i.e. pain lasting more than one-month
comorbidities affecting the nervous system
any disease requiring systematic drug consumption.
diagnosed hypersensitive reaction to saline solution
All locations for NCT03021278
The Jerzy Kukuczka Academy of Physical Education
Katowice, Poland, 40-065
View full eligibility
Tris trial is registered with FDA with number: NCT03021278. The sponsor of the trial is The Jerzy Kukuczka Academy of Physical Education in Katowice and it is looking for 57 volunteers for the current phase.
Official trial title: Lumbar Tactile Acuity in Experimentally Induced Acute Low Back Pain
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