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The Study of the Early Administration of Alendronate on Prevention of Bone Loss After Hip Fracture.

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McGill University

Status and phase

Unknown
Phase 3

Conditions

Osteoporosis

Treatments

Drug: Alendronate

Study type

Interventional

Funder types

Other
Industry

Identifiers

Details and patient eligibility

About

To determine whether administration of Alendronate early is more effective than late in the prevention of osteoporosis following a hip fracture

Sex

All

Ages

55+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Male and Female aged > 55 Low trauma hip fracture up to 90 days Be willing to submit to periodic bone mineral density radiographic studies of the spine & 24 hr urine collection Written informed consent

Exclusion criteria

  • Disorders known to affect bone metabolism Not taking bisphosphonates within last 6 months Drugs known to interfere with calcium metabolism within the lats 6 months prior to hip fracture serum calcium> 2.65 mmol/L Treatment with any investigational drug within the last 30 days

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

1

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Central trial contact

Giselle Charrette, RN CONc; Richard Kremer, MD PhD

Data sourced from clinicaltrials.gov

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