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Periprosthetic Plate Over Humeral Nail

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

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06812195
Acronym
osteoporosis
Enrollment
3
Registered
2025-02-06
Start date
2025-03-01
Completion date
2026-03-01
Last updated
2025-02-12

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

Conditions

Osteopenia, Osteoporosis

Keywords

deformity, osteoporosis

Brief summary

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

DEVICEPlate 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

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Under spinal anesthesia in supine position, lateral approach to the femur is used to do corrective osteotomies and introduction of humeral nail according to preoperative plan. After that, plate is applied to lateral border to the feoral shaft. Weight bearing is allowed after confirmation of union after 6 weeks. Regular visits every 3 months.

Eligibility

Sex/Gender
ALL
Age
16 Years to 40 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Metal failure2 yearsNumber of cases with bending or protrusion

Contacts

Primary ContactHesham m Elbaseet, MD
drhesham20@aun.edu.eg201007780689

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026