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Comparison of the effects two methods manual traction and automatic traction in femural fractures surgery

Comparison of the effects two methods manual traction and automatic traction in femural fractures surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210110049987N1
Enrollment
65
Registered
2021-02-13
Start date
2021-05-05
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

femural fractures surgery.

Interventions

Intervention 1: Intervention group: : The intervention group includes patients whose fractures will be implanted in the same period of time by automatic traction method. Automatic traction (use in the

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Need for femoral plate surgery

Exclusion criteria

Exclusion criteria: infection before surgery bleeding diseases any disturbance in coagulation tests mental retardation chronic underlying diseases (diabetes, cancer, etc.)

Design outcomes

Primary

MeasureTime frame
Pain score in McGill Questionnaire. Timepoint: After surgery. Method of measurement: .McGill Pain Questionnaire.;The duration of surgery is calculated based on minutes according to the surgery. Timepoint: The duration of surgery is measured in minutes from the moment the surgeon declares the need for traction until the two broken pieces are placed side by side. Method of measurement: Based on minutes spent using the clock at the surgery site.;The amount of musculoskeletal pain and discomfort based on the score obtained from the Nordic questionnaire. Timepoint: After surgery. Method of measurement: Nordic Ergonomics Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarzad Abaszadeh

Kerman University of Medical Sciences

fabaszadeh99@gmail.com+98 34 3226 4196

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026