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Not yet recruiting NCT06812195

Periprosthetic Plate Over Humeral Nail

No phase Interventional Osteopenia, Osteoporosis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Plate and nail.
Who it may be relevant to
Registry conditions: Osteopenia, Osteoporosis. Basic parameters: 16 years — 40 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Plate Over Humeral Nail in Deformity Correction of Femur in Adult Osteoporotic Bone

Overview

use of plate over humeral nail in deformity correction of femur in adult osteoporotic bone

Detailed description

small IM interlocking nail, such as humeral nail, could be used in femoral fixation in normal adolescent patients due to the advantages of the entry point lateral to tip of greater trochanter resulting in avoiding iatrogenic vascular injury and being the IM locking device with smaller diameter and shorter length than conventional femoral nail which was appropriate for small-sized adolescent femoral anatom

Interventions

  • Device Plate and nail
    spinal anesthesia in supine position, lateral approach to the femur is used to do corrective osteotomies and introduction of nail according to preoperative plan. After that, plate is applied to lateral border to the femoral shaft

Primary outcome measures

  • Metal failure [Time frame: 2 years]

Eligibility criteria

Inclusion criteria

  • Osteoporotic bone with femoral deformity.
  • Osteogenesis imperfecta. --Vitamin D deficiency ricket

Exclusion criteria

  • Uncooperative patient.

\-- Skeletally immature

  • Not receiving medical treatment.
  • Patient with history of allergy to drugs used in the study.
  • Neuromuscular pathology, previous trauma, or surgery to the leg

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Publications

  • Gordon JE, Khanna N, Luhmann SJ, Dobbs MB, Ortman MR, Schoenecker PL. Intramedullary nailing of femoral fractures in children through the lateral aspect of the greater trochanter using a modified rigid humeral intramedullary nail: preliminary results of a new technique in 15 children. J Orthop Trauma. 2004 Aug;18(7):416-22; discussion 423-4. doi: 10.1097/00005131-200408000-00004. PMID 15289686

Identifiers

NCT: NCT06812195 · PPON · PPOND

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗