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Clinical Trials/IRCT138801211804N1
IRCT138801211804N1CompletedPhase 2

Survey of therapeutic effect of oral prednisolone in compression of placebo in cervical radiculopathy treatment

Private0 sites60 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 2
Status
Completed
Sponsor
Enrollment
60

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 years to 60 years (—)
Sex
All

Inclusion Criteria

  • Inclusion Criteria: 1- Age 60-18 years. 2- Arm and neck pain consistent with cervical radiculopathy. 3- Neck disability scale (NDI) at least 15 (moderate disability). 4- The onset of symptoms between 2 weeks to 1 month. 5- No chronic use of corticosteroid. 6- No a history of previous surgery of cervical spine. Exclusion criteria: 1- Patients with immunosupression. 2- Red flag of tumor and clinical infection. 3- Symptoms of myelopathy. 4- Liver failure. 5- Schizophrenia. 6- Pregnancy and lactation. 7- Diabetes. 8- Osteoporosis. 9- Glaucoma. 10- Peptic ulcer. 11- Normal EMG after one month.

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Private

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