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Comparison of effectiveness of corticosteroid with dextrose in treatment of carpal tunnel syndrome.

Comparison of the effectiveness of ultrasound-guided local corticosteroid injection with dextrose 5% solution injection in carpal tunnel syndrome.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180603039969N1
Enrollment
54
Registered
2019-12-12
Start date
2019-12-10
Completion date
Unknown
Last updated
2020-08-17

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

Interventions

Intervention 1: One session of ultrasound-guided 1 CC Triamcinolone (Exir co, Tehran, Iran) injection into the carpal tunnel. Intervention 2: One session of ultrasound-guided 5 CC dextrose 5% solution

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with clinical diagnosis of carpal tunnel syndrome (paresthesia over the median nerve territory in the hand). Mild to moderate severity of carpal tunnel syndrome, based on electrodiagnostic studies. Age between 18-65 years,

Exclusion criteria

Exclusion criteria: Severe CTS ( based on electrodiagnostic data). Signs of thenar atrophy. Contraindication for injection ( such as history of hypersensitivity to corticosteroid, signs of local infection, immune deficiency, needle phobia. Diseases that mimic symptoms of carpal tunnel syndrome such as polyneuropathy, radiculopathy, and thoracic outlet syndrome. Surgical treatment or local injection in the last six months. Neoplastic or traumatic origin. Tenderness and fracture of wrist bones.

Design outcomes

Primary

MeasureTime frame
Pain intensity (Visual analogue scale). Timepoint: Baseline, and after 2 weeks, one month and 6 months after injection. Method of measurement: 10 point VAS scale.;Electrodiagnosis parameters. Timepoint: Baseline, and after 2 weeks, one month and 6 months after injection. Method of measurement: Electrodiagnostic study machine.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSara moradnia

Iran University of Medical Sciences

moradnia.s@ajums.ac.ir+98 21 6435 2683

Outcome results

None listed

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