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Outcomes of subtrochanteric and intertrochanteric fracture fixation using DHS and TSP plates compared with anti-DHS and DCP plates

Evaluation the outcome of fixation of subtrochanteric and intertrochanteric fracture (class A3) of femur using DHS plate with anti-sliding (ASP) and DHS plate with stabilizing lateral wall of proximal femur.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20251001067448N1
Enrollment
100
Registered
2026-01-28
Start date
2024-04-26
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Pertrochanteric fracture. Pertrochanteric fracture

Interventions

Intervention 1: First intervention group: During the surgery, following exposure of the fracture through a lateral incision on a standard operating table, the fracture will be reduced using appropriat

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Having an A3 intertrochanteric and subtrochanteric fracture Desire for surgery and fixation with a plate

Exclusion criteria

Exclusion criteria: Presence of a disease affecting the bone (chronic renal failure, primary tumor, metastasis, etc.)

Design outcomes

Primary

MeasureTime frame
Healing of the fracture site. Timepoint: 1 month after intervention, 3 months after intervention, and 6 months after intervention. Method of measurement: Radiography.;Delayed union. Timepoint: 1 month after intervention, 3 months after intervention, and 6 months after intervention. Method of measurement: Radiography.

Secondary

MeasureTime frame
Postoperative varus deformity. Timepoint: 1 month, 3 months and 6 months after surgery. Method of measurement: Radiography.;Shortening of the femur. Timepoint: 1 month, 3 months and 6 months after surgery. Method of measurement: Radiography.;Pain intensity after fixation. Timepoint: 1 month, 3 months and 6 months after surgery. Method of measurement: Visual analogue scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadreza Sadeghi

Hamedan University of Medical Sciences

moresa49@gmail.com????????????

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026