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Dynamic condylar screw combined with anatomic medial supporting plate in the treatment of nonunion after intertrochanteric fracture: a retrospective study based on medical records

Dynamic condylar screw combined with anatomic medial supporting plate in the treatment of nonunion after intertrochanteric fracture

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000033598
Enrollment
Unknown
Registered
2020-06-06
Start date
2020-07-01
Completion date
Unknown
Last updated
2020-06-08

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

Conditions

intertrochanteric nonunion

Interventions

experimental group:DCS Combined with MABP

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age: 18-79 years old; 2. Intertrochanteric nonunion; 3. The revision operation is: dynamic condylar screw (DCS) combined with anatomical medial buttress plate (MABP) 4. The subjects must be able to talk normally and understand the questions in the "subject subjective questionnaire", and be able to provide feedback in appropriate language;

Exclusion criteria

Exclusion criteria: 1. Allergic to implant; 2. There are clear contraindications to anesthesia and operation; 3. Serious cartilage injury of hip; 4. Avascular necrosis of the femoral head (Ficat stage 3 and 4); 5. Severe hip osteoarthritis (K-L grade 4); 6. Severe loss of bone mass in the proximal femur can not achieve the effective fixation of the internal fixation; 7. There is nonunion in other parts of the extremities, and surgery is needed at the same time or successively; 8. Postoperative nonunion of pathological fracture (such as primary or metastatic tumor); 9. Some medical diseases are not suitable for inclusion in the study, such as diabetes, metabolic osteopathy, sequelae of poliomyelitis, secondary severe osteoporosis (such as hyperparathyroidism), etc; 10. There was infective nonunion in the femoral intertrochanteric fracture of the affected side, or there was infective nonunion in other parts of the limb; 11. Segmental bone defect >= 6cm; 12. Cancer patients are undergoing chemotherapy or radiotherapy, or patients with other diseases are receiving systemic corticosteroids; 13. The patient has participated in other clinical trials in the past 3 months; 14. Patients may have poor compliance, which is not suitable for inclusion (such as daily excessive drinking or smoking, drug taking) according to the judgment of researchers; 15. Patients with poor compliance were judged by the researchers to be unable to complete the trial according to the research plan, such as schizophrenia and dementia.

Design outcomes

Primary

MeasureTime frame
Lower extremity functional scale;fracture healing rate;fracture healing time;

Countries

China

Contacts

Public ContactZhang Wei

Chinese PLA General Hospital

Zwtyrran@163.com+86 15210011027

Outcome results

None listed

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