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A Norwegian trial Comparing Treatment Strategies for Carpal Tunnel Syndrome

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-511223-34-00
Enrollment
258
Registered
2024-06-19
Start date
2022-04-08
Completion date
Unknown
Last updated
2024-06-19

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

Conditions

Carpal Tunnel Syndrome

Brief summary

Successful treatment outcome after one year, defined as attainment of Boston Carpal Tunnel Questionnaire Symptom Score ≤ 1.5

Detailed description

Successful treatment result (as defined above) after 3, 6 and 24 months, Successful treatment result after one injection, and after two injections, Patients in the injection arm who have undergone surgery after 3 weeks, 3, 6, 12 and 24 months, Work performance/participation and health care utilization as outlined in section 8.8 at each, or a combination, of time points., Adverse events throughout the study, Patient-reported measures of symptoms and function, ultrasound and NCS measures as outlined in section 8.1 at each time point, Emitted CO2-equivalents per treatment strategy pathway.

Interventions

DRUGTrica 20 mg/ml injeksjonsvæske
DRUGLederspan 20 mg/ml injeksjonsvæske
DRUGsuspensjon.

Sponsors

Diakonhjemmet Sykehus AS
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Successful treatment outcome after one year, defined as attainment of Boston Carpal Tunnel Questionnaire Symptom Score ≤ 1.5

Secondary

MeasureTime frame
Successful treatment result (as defined above) after 3, 6 and 24 months, Successful treatment result after one injection, and after two injections, Patients in the injection arm who have undergone surgery after 3 weeks, 3, 6, 12 and 24 months, Work performance/participation and health care utilization as outlined in section 8.8 at each, or a combination, of time points., Adverse events throughout the study, Patient-reported measures of symptoms and function, ultrasound and NCS measures as outlined in section 8.1 at each time point, Emitted CO2-equivalents per treatment strategy pathway.

Countries

Norway

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026