CTRI/2022/05/042711Not yet recruitingPhase 3
To compare the efficacy of suprascapular nerve block using local anaesthetic and two different doses of steroid in cervical radicular pain
PtBDSharma PGIMS ROHTAK0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 3
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •Patients fulfilling following three criteria will be included in the study:
- •Ã¢â?¬Â¢History, physical examination and pain pattern consistent with cervical radiculopathy.
- •Ã¢â?¬Â¢X-ray cervical spine or MRI findings corresponding with the patientââ?¬•s clinical symptoms.
- •Ã¢â?¬Â¢Failure to respond to six weeks of conservative treatment.
Exclusion Criteria
- •Patients with
- •Ã¢â?¬Â¢History of uncontrolled diabetes mellitus
- •Ã¢â?¬Â¢Active infection or active wound at the suprascapular, cervical and upper limb areas.
- •Ã¢â?¬Â¢Known contraindications to nerve block in suprascapular, neck and shoulder areas
- •Ã¢â?¬Â¢Recent history of severe trauma to the suprascapular, neck and upper limb
- •Ã¢â?¬Â¢History of suprascapular nerve block injection in the past three months
- •Ã¢â?¬Â¢History of allergy or adverse reaction to the injecting agents
- •Ã¢â?¬Â¢History of severe chronic airway or cardiovascular ir cerebrovascular disease
- •Ã¢â?¬Â¢History of systemic use of steroid two weeks before the injection
- •Ã¢â?¬Â¢Ongoing pregnancy or breastfeeding
- •Ã¢â?¬Â¢Pain in upper limb due to conditions like osteoarthritis, rheumatoid arthritis, frozen shoulder
Investigators
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