Last updated: October 18, 2023
Sponsor: C.L.A.Vleggeert-Lankamp
Overall Status: Active - Recruiting
Phase
N/A
Condition
Sciatica
Radiculopathy
Treatment
Methylprednisolone Acetate
Lidocaine
Dexamethasone
Clinical Study ID
NCT03924791
TEIAS
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
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
Exclusion Criteria:
- Age under 18 years
- Condition preventing to receive transforaminal epidural injection
- Severe scoliosis
- Transforaminal epidural injection received in 6 months before randomization date
- Surgery for sciatica at the same level
- Surgery for sciatica at another level within one year before inclusion
- Pregnancy
Study Design
Total Participants: 142
Treatment Group(s): 3
Primary Treatment: Methylprednisolone Acetate
Phase:
Study Start date:
June 01, 2019
Estimated Completion Date:
July 31, 2026
Study Description
Connect with a study center
Spaarne Gasthuis
Haarlem,
NetherlandsActive - Recruiting
Spaarne Gasthuis
Hoofddorp,
NetherlandsActive - Recruiting

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