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Recruiting NCT05712616

Role of Strontium Ranelate in Proximal Femur Fragility Fractures.

Conditions: Fragility Fracture, Femur; Fracture, Pertrochanteric, Clinical Trial

Sex: All
Ages: 60 Years – 100 Years
Phase: PHASE4
Enrollment: 100
Sponsor: Aga Khan University Hospital, Pakistan

Location: Pakistan

Summary

This study is being conducted with the aim of comparing the time to bone healing after surgery for fragility fractures of proximal femur between patients receiving strontium ranelate and placebo. Patients recruited are of 60 years of age and above. Bone healing will be assessed on clinical parameters when patient is able to ambulate full weight bearing without pain and on Xray images using RUSH score. Moreover Dexa scan will be performed pre-operatively and at 3 months postoperatively. The findings of this study will help in setting up guidelines for treatment of fragility proximal femur fractures in our population as there is still paucity of literature on effectiveness of strontium ranelate from our part of the world.

Eligibility Criteria

Inclusion Criteria:All patients with age =/> 60 years with proximal femur fracture including per-trochanteric, sub-trochanteric and neck of femur fractures amnebale to ORIF.ORIF will include hip cannulated screws, dynamic hip screw and intra-medullary nails.Exclusion Criteria:Patients with metabolic bone diseases.Patients with pathological fractures like tumor, osteopetrosis etc.Patients with prior Ischemic heart diseases and underwent PCI or CABG

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05712616). StuddyBuddy aggregates publicly available trial information.