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Efficacy of Me-Cal in osteoporosis patients as compared to standard calcium supplement

Not Applicable
Conditions
Health Condition 1: null- OSTEOPOROSIS
Registration Number
CTRI/2018/01/011309
Lead Sponsor
SG PHYTO PHARMA PVT LTD
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Patients complaining of classical symptoms of

joint pain, pain in the bones etc. which will

be confirmed later by the BMD-test with BMD

score below -1.

2. Patient agrees not to use any other calcium

supplement for osteoporosis other than what is

provided by the study.

3. Patient agrees to written informed consent.

4. Patient willing to participate in the study

for 12 weeks.

5. Patient who has not participated in any

clinical study in last 30 days.

Exclusion Criteria

1.Planning to conceive, pregnant and lactating mothers.

2. Patient under osteoporosis treatment.

3. Patients suffering from heart disease.

4. Patients with severe renal impairment.

5. Patient with known metabolic bone disease such

as osteogenesis imperfecta, or currently

healing fractures of lumbar spine, hips or

femurs.

6. Patient on current treatment with steroids or

chemotherapy.

7. History of malignancy

8. History of hypersensitivity to any of the investigational drugs.

9. History of psychiatric disorder that may impair the ability of subjects to provide written informed consent

10. Any medical condition, where the investigator feels participation in the study could be detrimental to the subjects overall well-being.

Study & Design

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