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A clinical trial to study the effects of two treatment modalities in patients of Carpal Tunnel Syndrome.

Prospective evaluation of pain relief and dynamic mobility of median nerve, using ultrasound following corticosteroid injection and carpal tunnel release in patients with carpal tunnel syndrome. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073211
Enrollment
60
Registered
2024-09-02
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: G560- Carpal tunnel syndrome

Interventions

Intervention1: Corticosteroid Injection therapy: Comparison of functional outcome in patients of carpal tunnel who have undergone corticosteroid injection therapy and carpal Tunnel release surgery

Sponsors

Dr RMLIMS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - Clinical diagnosis of Carpal Tunnel Syndrome, with duration more than six months not responding to conservative measures including non-steroidal anti-inflammatory drugs (NSAIDS), - Patient willing to participate in the study after proper Informed Consent taking.

Exclusion criteria

Exclusion criteria: - Earlier surgery like Ultrasound Guided Carpal Tunnel Release or Open Carpal Tunnel Release, - Local Corticosteroid injection within the last 6 months, - Patients who have received Platelet Rich Plasma Therapy for Carpal Tunnel Syndrome. - Physical therapy within 6 weeks, image proved rupture or conditions in which non-steroidal anti-inflammatory drugs were used within 1 week, - History of severe anemia (Hemoglobin less than 5), - Thrombocytopenia or Bleeding tendency, - Vascular insufficiency (Impalpable Radial Pulse) - Neuropathy which is related to pain.

Design outcomes

Primary

MeasureTime frame
Assessment of Improvement in the Pain levels of the patient undergoing the two interventions by VAS Score and BCTQ Scale.Timepoint: 1. Before procedure 2. Right after procedure 3. 1 week 4. 1 month 5. 3 months 6. 6 months

Secondary

MeasureTime frame
Median nerve crosssectional area and mobility using ultrasonographic measurement.Timepoint: Ultrasonographic assessment pre and post intervention at different time intervals up to 6 months.

Countries

India

Contacts

Public ContactShivani Rastogi

Dr RMLIMS

neuromanu@yahoo.com8176007201

Outcome results

None listed

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