Randomized control study of comparison of the amount of intraoperative radiation exposure using distal targeting device

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002800

Enrollment

Registered

2018-04-16

Start date

2018-02-06

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 : Arm 1 (Experimental) : Fix the distal interlocking screw using distal targeting device. Arm 2 (Active comparator) : Fix the distal interlocking screw using freehand (without distal

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Femur unstable intertrochanteric fracture and subtalar fracture using long cephalomedullary nail for patients older than 60 years who require internal fixation

Exclusion criteria

Exclusion criteria: 1) Pathological fracture due to tumor 2) Patients with reoperation due to nonunion

Design outcomes

Primary

Measure	Time frame
Radiation dose calculated from patient's surgeon's TLD-100 (LiF)	—

Secondary

Measure	Time frame
Operation time	—

Countries

Korea, Republic of

Contacts

Public ContactJun-Il Yoo

Gyeongsang National University Hospital

furim@daum.net+82-55-750-9787

Outcome results