FindTrial
Sign In

Design and Clinical Application of A Novel Instrument for Femoral Shaft Fracture

Efficacy of Fracture Reduction Device and Guidewire Aiming Device in Intramedullary Nail Internal Fixation for Femoral Shaft Fracture: a Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-ICR-15007335
Enrollment
Unknown
Registered
2015-11-01
Start date
2011-02-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Femoral shaft fracture

Interventions

Experimental group:Novel instrument
Control group:Normal surgical method

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 58 Years

Inclusion criteria

Inclusion criteria: Patients were included in the cohort if they (1) were not beyond 60 years old; (2) had a unilateral traumatic closed fracture of the upper section of the femoral shaft, which was totally displaced; (3) were 32.A or 32.B fracture pattern according to the AO/OTA classification; (4) were to be treated by closed reduction and anterograde interlocking intermedullary nail; (5) underwent operation in 7d from the injury.

Exclusion criteria

Exclusion criteria: Patients were excluded from the study if they had (1) open fracture; (2) multiple fractures; (3) pathologic fracture; (4) declined to participate in this cohort.

Design outcomes

Primary

MeasureTime frame
Frequency of drilling attempts;case of open reduction;Operative time;—

Secondary

MeasureTime frame
Blood Loss;Duration of hospital stay;—

Countries

China

Contacts

Public ContactSHENG Jiagen
jiagen_sheng@163.com+86 18930174886

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 1, 2026