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Alendronate for the prevention of osteoporosis in ankylosing spondylitis

Phase 2
Conditions
Ankylosing spondylitis.
Ankylosing spondylitis
Registration Number
IRCT201212206975N3
Lead Sponsor
Vice chancellor for research, Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
20
Inclusion Criteria

Schober index=5; Normal hip joint in the pelvic radiography; Absence or rarity of syndesmophyte in the spine radiography (Taylor index=1); Normal bone density or mild osteopenia (T-score=-1.5)
Exclusion criteria:
Use of drugs which increase bone density like bisphosphonates; Use of steroids and biological agents; Coexistence of other disease which decreases bone density: including hyperparathyroidism, diabetes, hyper and hypothyroidism, osteomalasia, liver failure, renal failure

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Bone density. Timepoint: 12 months after intervention (at the end of study). Method of measurement: Bone mineral density measurement as gram/cm² by the DEXA method with Hologic QRD model instrument from lumbar and pelvic area.
Secondary Outcome Measures
NameTimeMethod
Osteoporotic fracture. Timepoint: Every 3 months until 12 months. Method of measurement: History, physical examination, and radiography.
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