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Comparison of efficacy of ultrasound-guided midline and ulnar in-plane approach and blind midline approach triamcinolone acetonide injection in pain and fuction improvement among patients with carpal tunnel syndrome; A randomized clinical trial.

Comparison of efficacy of ultrasound-guided midline and ulnar in-plane approach and blind midline approach triamcinolone acetonide injection in pain and fuction improvement among patients with carpal tunnel syndrome; A randomized clinical trial.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130523013442N25
Enrollment
40
Registered
2018-09-16
Start date
2018-09-01
Completion date
Unknown
Last updated
2018-10-11

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

Conditions

carpal tunnel syndrome. Carpal tunnel syndrome, unspecified upper limb

Interventions

Intervention 1: Intervention group: Local ulnar in-plane injection of triamcinolon 40 mg by ultrasound. Intervention 2: Intervention group: Local midline in-plane injection of triamcinolon 40 mg by

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients who suffer from mild or moderate carpal tunnel syndrome. Participants aged between 18 to 65 years Patients who had symptoms for at least 3 months

Exclusion criteria

Exclusion criteria: Women who were pregnant Participants who had severe carpal tunnel syndrome Patients who had past history of disorders like diabetes mellitus, thyroid dysfunction and rheumatoid arthritis Patients who had history of local injection of steroids within last 3 months Patients who had concomitant underlying neuropathy or radiculopathy

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before intervention and 10 weeks after injection. Method of measurement: Visual Analogue Scale.;Function. Timepoint: Before intervention and 10 weeks after injection. Method of measurement: Boston questionnaire.;Sensory and motor nerve conduction. Timepoint: Before intervention and 10 weeks after injection. Method of measurement: Nerve electrophysiologic study.;Median nerve size in ultrasound. Timepoint: Before intervention and 10 weeks after injection. Method of measurement: Cross section area of median nerve in inlet of carpal tunnel by ultrasound.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Ahmadi Dastgerdi

Shahid Beheshti University of Medical Sciences

Mo.ahmadi1370@gmail.com+98 21 2236 3244

Outcome results

None listed

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