Evaluating of the Korean version of self-administered outcome instrument and comparison of treatment method.

Evaluating of the Korean version of self-administered outcome instrument for the assessment of severity of symptoms and functional status and diagnostic value of sonography in patients of carpal tunnel syndrome and comparison of treatment method.

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CRIS

Registry ID

KCT0000050

Enrollment

100

Registered

2010-10-21

Start date

2010-10-01

Completion date

Unknown

Last updated

2019-03-11

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

Conditions

None listed

Interventions

Procedure/Surgery : Comparison of treatment of carpal tunnel syndrome

local steroid treatment vs sugical treatment

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients will be enrolled into this study, if the following criteria was fulfilled 1. symptom of carpal tunnel syndrome A. pain of weist or hand B. tingling sensation or numbness C. weakness D. nocturnal aggravation of symptoms E. Tinel sign, phalen sign 2. confirmatory electrophysiologic results A. distal motor latency of median nerve > 4.0ms or B. distal sensory latency of median nerve > 3.4ms C. median-ulnar palmar sensory lstency difference > 0.5ms

Exclusion criteria

Exclusion criteria: Exclusion criteria a. histroy of wrist surgery b. carpal tunnel syndrome caused by trauma c. neurologic disorder mimicing carpal tunnel synrome such as,cervical radiculopathy, polyneuropathy, proximal median neuropathy

Design outcomes

Primary

Measure	Time frame
validation of self-admistered instrument of carpal tunnel syndrome;cross-sectional area by sonography	—

Secondary

Measure	Time frame
treatment efficasy	—

Countries

Korea, Republic of

Contacts

Public ContactDong-jin Park

Chonnam National University Hospital

Outcome results