Improve the Efficiency of Surgery for Guide wire insertion for PFNA with Radiolucent tempalte: A Randomized Controlled Trial

Phase 2

Active, not recruiting

• Conditions: - Unstable intertrochanteric fracture

• Registration Number: TCTR20171212001
• Lead Sponsor: one

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-12-12
• Study Completion: 2019-03-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Active, not recruiting
• Sex: All
• Target Recruitment: 39

Inclusion Criteria

- Unstable intertrochanteric fracture
(AO-OTA: 31A1, 31A2.1, 31A2.2, 31A2.3, 31A3)

Exclusion Criteria

- BMI > 40
- An open fracture
- Multiple fracture
- Pathologic fracture except osteoporosis
- History of previous musculoskeletal disease of the same hip
- History of prevoius surgery of the same hip

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Guide wire insertion time in AP view Start when performimg guide wire insertion and finish when completing the insertion second

Secondary Outcome Measures

Name	Time	Method
Fluoroscopic time Time that the surgeon uses the fluoroscopy (start when perfornimg guide wire insertion and finish wh second,Number of drilling Frequency of drilling the guide wire median,Successful Tip&#45;Apex distance (TAD) Using the radiograph post operatively ( TAD < 25 is acceptable) Percentage