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A comparison between corticosteroid injection versus local anaesthetic in treatment of elbow tendinitis

A comparison between corticosteroid injection versus local anaesthetic in treatment of lateral epicondylitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201205127274N4
Enrollment
90
Registered
2012-05-30
Start date
2012-04-20
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lateral epicondylitis.

Interventions

Intervention 1: Group 2: Corticosteroid (Methyl-prednisolon acetate 1 ml) injection single dose into the painful zone. Intervention 2: Group 1: injection of a local anesthesia (procaine 2% 1 ml).
Treatment - Drugs
Group 2: Corticosteroid (Methyl-prednisolon acetate 1 ml) injection single dose into the painful zone
Group 1: injection of a local anesthesia (procaine 2% 1 ml)

Sponsors

Vice Chancellor for Research, Guilan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria:chronic pain in lateral zone of elbow; definite tenderness in lateral epicondylitis; age more than 15 years and VAS score more than 6. Exclusion criteria: radicular pain to the upper limbs; established Carpal Tunnel Syndrome and past history of tennis elbow treatment.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Disability of elbow score. Timepoint: At baseline, and 3, 6, 12 weeks after treatment. Method of measurement: The Disabilities of the Arm, Shoulder and Hand Score(QuickDash).

Secondary

MeasureTime frame
Pain severity. Timepoint: At baseline, and 3, 6, 12 weeks after treatment. Method of measurement: Value-added service (VAS) score.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mohsen Mardani Kivi

Guilan University of Medical Science

dr_mohsen_mardani@yahoo.com+98 13 1321 1470

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026