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Effects of ultrasound guided injection of hyaluronic acid in managment of carpal tunnel syndrome

Effects of ultrasound guided injection of hyaluronic acid in managment of carpal tunnel syndrome; A randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130523013442N27
Enrollment
40
Registered
2019-05-29
Start date
2019-04-21
Completion date
Unknown
Last updated
2019-08-26

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 1cc hyalouronic acid with 0/5 cc lidocaine 2% by ultrasound. Intervention 2: Control group: Local ulnar in-plane injection of 1cc

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
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.;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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarzieh Shakoori Arani

Shahid Beheshti University of Medical Sciences

m.shakoori1269@gmail.com+98 21 2236 3244

Outcome results

None listed

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