Transforaminal Epidural Injection in Acute Sciatica

Recruiting N/A Interventional Study
Sciatica Sciatica Due to Intervertebral Disc Disorder Sciatic Radiculopathy
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
142 (estimated)
Sponsor
C.L.A.Vleggeert-Lankamp · Other
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About This Trial
Patients suffering from sciatica are treated conservatively for the first 8 weeks due to the favourable prognosis. This period is preferably extended up to 14-16 weeks after which patients may opt for surgery. However, patients may experience severe discomfort due to pain in the leg which can lead to decreased physical activity and socio-economic problems. An adequate therapy to alleviate symptoms…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Diagnosed with sciatica by GP * NRS leg pain of 6 or more on a 10-point NRS scale * Minimum duration of symptoms of 3 weeks and maximum duration of 8 weeks Exclusion Criteria: * Age under 18 years * Condition preventing to receive transforaminal epidural injection * Severe s…
Contacts

Carmen LA Vleggeert-Lankamp, MD Msc Ph.D

+31715262109

cvleggeert@lumc.nl

CONTACT

Eduard JA Verheijen, Bsc

+31715262109

e.j.a.verheijen@lumc.nl

CONTACT