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A clinical trial to assess the effect on quality of life in post menoapausal osteoporotic women with salmon calcitonin nasal spray.

Phase 4
Completed
Conditions
Health Condition 1: null- postmenopausal osteoporosis
Registration Number
CTRI/2010/091/002958
Lead Sponsor
Glenmark Pharmaceuticals Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
40
Inclusion Criteria

a.Postmenopausal women between 45-65 years of age or surgical menopausal (oophorectomy) cases

b.Bone mineral density(BMD) values -2.5 SD in at least one region measured by Dual Energy X-ray absorptiometry (DEXA)

Exclusion Criteria

a.Presence of secondary causes of osteoporosis and other possible causes of back pain (fragility fracture ,bone metastasis or inflammatory spine disease such as spondylarthritis)

b.Use of medications that cause osteoporosis

c.Any contraindications for using salmon calcitonin or calcium

d.History of taking anti osteoporotic agents in the last month

Study & Design

Study Type
PMS
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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