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Comparison of two therapeutic methods in patients with pain in the lateral part of elbow

Comparing the effects of sono-guided local dexamethasone injection with dexamethasone phenophoresis in treating lateral epicondylitis (tennis elbow)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201407014422N5
Enrollment
60
Registered
2014-07-17
Start date
2013-12-22
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. Lateral epicondylitis

Interventions

Intervention 1: In control group, sono-guided injections were performed in common extensor tendon junction. Injection of 8 milligrams of dexamethasone and 1 cc of lidocaine will be performed for 10 se
Treatment - Drugs
Treatment - Devices
In control group, sono-guided injections were performed in common extensor tendon junction. Injection of 8 milligrams of dexamethasone and 1 cc of lidocaine will be performed for 10 sections
In Intervention group, ultrasound probe will be put on dexamethaosne cream applied on lateral part of elbow with 1 MHz frequency and 1w/cm2 power for 5 minutes

Sponsors

Vice chancellor for research, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Pain and tenderness in lateral parts of elbow lasting more than three moths, exacerbation of pain while arm supination, flexion and wrist dorsiflexion against resistance. Exclusion criteria: History of connective tissue disorders or diffuse pain syndrome, inflammatory arthropathy, using anti-coagulant drugs, contraindications for local injection and radiculopathy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Patients' pain. Timepoint: Before intervention, one month and 3 months after intervention. Method of measurement: By using visual analogue scale.;Grasping power. Timepoint: Before intervention, one month and 3 months after intervention. Method of measurement: By using a dinamometer.;Patients' functional disability. Timepoint: Before intervention, one month and 3 months after intervention. Method of measurement: Bu using PRTEE questionnare.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Farzaneh Johari

Tabriz University of Medical Sciences

farzanehjohari@ymail.com+98 41 1334 1317

Outcome results

None listed

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