Effects of Bisphosphonates and Nutritional Supplementation After a Hip Fracture
Hip Fracture
About this trial
This is an interventional prevention trial for Hip Fracture focused on measuring Hip fracture, Nutritional supplement, Bisphosphonates, Bone mineral density, Body composition
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 60 years
- Recent fracture of the femoral neck or trochanter
- Without severe cognitive impairment
- Ambulant before fracture
- BMI ≤ 28
Exclusion Criteria:
- Abnormal parameters regarding liver i.e. S-Alanine aminotransferase (S-ALAT) and S-Aspartate aminotransferase (S-ASAT) ≥ twice as normal
- Abnormal parameters regarding kidney i.e. S-Creatinine > 130 µg/L
- Primary hyperparathyroidism, osteogenesis imperfecta, Paget´s disease
- Myeloma
- Lactose intolerance
- Dysphagia
- Esophagitis
- Gastric ulcer
- Malignancy
- Diabetes with nephropathy or retinopathy
- Active iritis or uveitis
Sites / Locations
- Department of Geriatric Medicine R94, Karolinska University Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
Active Comparator
Risedronate
Nutritional supplement
Calcium and vitamin D3
35 mg risedronate orally administered once weekly for 12 months and orally administered Calcium 1000 mg and 800 IU vitamin D3 daily for 12 months. Group B (bisphosphonate group)
Oral liquid nutritional supplement (600kcal and 40 gram protein/day) for 6 months after the hip fracture besides Risedronate and calcium and vitamin D3. Group BN (bisphosphonate and nutritional supplemented group)
An oral dose of 1000 mg Calcium and 800 IU vitamin D3 daily for 12 months after hip fracture. Group C (control)