Ultrasound stimulating treatment for intertrochanteric fracture

Clinical Efficacy and Safety of Ultrasound stimulating treatment for intertrochanteric fracture patients

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002591

Enrollment

Registered

2017-12-15

Start date

2017-10-24

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

Medical Device : The experimental group applys 20 minutes of ultrasound stimulating treatment and coventional treatment for 4 weeks (twice/day). Comparator group will receive conventional treatment fo

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Age of 65 to 85 years 2) Hip surgery patients with intertrochanteric fracture 3) Ability to understand and follow simple explanations and commands

Exclusion criteria

Exclusion criteria: 1) Recent medical emergency treatments 2) Knee joint replacement surgery 3) Anatomical fracture of corresponding side 4) Severe physical conditions of upper and lower extremities 5) Treatment of steroid medicine 6) Treatment of anticoagulant medicine 7) Other severe conditions not able to participate in the treatments 8) Currently participating other clinical trial test

Design outcomes

Primary

Measure	Time frame
bone union grade by CT	—

Secondary

Measure	Time frame
bone union grade by x-ray;Visual Analogue Scale;12-Item Short Form Health Survey Questionnaire	—

Countries

Korea, Republic of

Contacts

Public ContactKap-Soo Han

Chonbuk National University Hospital

hanks@jbnu.ac.kr+82-63-259-3462

Outcome results