Health Condition 1: G629- Polyneuropathy, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Willingness of patient to participate in study. 2)Patient age between 20-60 yrs 3)Clinically and Electrophysiologically diagnosed as Carpal Tunnel Syndrome since last 6 weeks. 4)Either sex.
Exclusion criteria
Exclusion criteria: 1)History of trauma. 2)Cervical radiculopathy. 3)Known patients of peripheral neuropathy of any other cause. 4)Pronator dysfunction 5)Patients having prior history of injectable corticosteroid 6) Patients with Motor dysfunction of the affected hand.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To determine effect of neuroplasty on different grades of median nerve dysfunction in carpal tunnel syndrome using Numerical Rating Scale.Timepoint: Patients will be assessed at 1;2;4 and 6 weeks post intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the effect of Neuroplasty on different grades of median nerve dysfunction using NCS. 2) To correlate the changes of median nerve cross sectional area on USG with Neurological Rating Scale and Nerve Conduction Studies before and after neuroplasty in different grades of median nerve dysfunction.Timepoint: Patients will be assessed at 1;2;4 and 6 weeks post intervention | — |
Countries
India
Contacts
AMU