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To study the effects of CollagenCal? in the management of Osteoporosis in women.

A RANDOMIZED, OPEN LABEL, MULTI-CENTER, TWO ARMS PARALLEL GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF CollagenCal� IN COMPARISON WITH A FORMULATION CONTAINING CALCIUM + VITAMIN D3 IN THE MANAGEMENT OF OSTEOPOROSIS IN WOMEN

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2012/05/002631
Enrollment
60
Registered
2012-05-07
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M810- Age-related osteoporosis without current pathological fracture

Interventions

Intervention1: CollagenPeptide + VitaminD3 + VitaminC + Calcium Citrate : 10mg Once Daily ORAL To be taken with Water for 12 months Control Intervention1: Calcium + VitaminD3: 10mg ORAL TABLET to be t

Sponsors

Nitta Gelatin India Limited
Lead Sponsor
Auroville Healthcare R D Pvt Ltd
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Subjects whoare ambulatory women of 40 to 65 years oldWhoare willing to give informed consent Whoare willing to comply with the study procedures and restrictions are diagnosed by DEXA as osteoporotic, with BMD score of T are diagnosed with Primary osteoporosis

Exclusion criteria

Exclusion criteria: ? Subjects who are previously diagnosed with secondary osteoporosis or got presently diagnosed by clinical lab investigations. ? Subject who are having a BMI of more than 30 ? had or has fracture, as observed from medical history with in past 6 months. ? Subjects who had hysterectomy ? Subjects who had received glucocorticoids, estrogens, thyroid hormone, parathyroid hormone, fluoride, bisphosphonates, calcitonin, thiazide diuretics, barbiturates, antiepileptic medication for the past 3 months. ? Subjects who are suffering from systemic diseases (cardiac, hepatic, renal, hemopoietic) which the investigator feels will compromise the subject?s safety. ? Subjects who are suffering from disorder that compromises the ability of the subject to give written informed consent and/or to comply with study procedures. ? Pregnant, lactating women and women of child bearing potential, not practicing effective methods of contraception and planning a pregnancy during the study period. ? Subjects who are known to have or tested positive for human immunodeficiency virus, hepatitis C virus, or hepatitis B surface antigen ? Any other metabolic bone disease or secondary cause to bone loss that is not controlled and will interfere with the interpretation of the findings. ? Malignancy ? Subjects who had or has received any organ or bone marrow transplantation. ? Any laboratory abnormality which, in the opinion of the investigator, will prevent the subject from completing the study or interfere with the interpretation of the study results. ? Subjects who are known to have calcium intolerance. ? Any physical or psychiatric disorder which, in the opinion of the investigator, will prevent the subject from completing the study or interfere with the interpretation of the study results. ? Alcohol or substance-abuse or smoking within the last 3 months. ? Subjects who recently underwent gastro-intestinal contrast studies and/or radionuclide tests before one week. ? Subjects who are having serum Creatinine1.3mg/dL, Serum calcium 10 mgl/dL. ? Subjects who are having systolic BP 175 mm Hg or diastolic BP 105mm Hg. ? Subject?s who are in suspect of primary hyperparathyroidism with serum calcium 10mg/dL combined with PTH 5.0 mmol/L or serum calcium 9.8mg/dL combined with PTH ≥7.0 mmol/L. ? Subjects who used Ayurvedic formulation or any form of CAM (Complementary Alternative Medicine) therapy in the preceding 3 months ? Subjects who are currently enrolled or participated in the any other trial(s) in preceding 3 months

Design outcomes

Primary

MeasureTime frame
Percentage decrease in the following markers from baseline to end of Treatment period o Serum â?? CTx: 23- 35% o Serum OC and Serum BAP : 13- 20% o Free Urinary DPD : 13 - 20% Timepoint: Percentage Decrease in the following Markers from Baseline to 6months and End of Treatment o Serum â?? CTx: 23- 35% o Serum OC and Serum BAP : 13- 20% o Free Urinary DPD : 13 - 20%

Secondary

MeasureTime frame
â?¢ Increase in percentage of BMD from baseline to the end of treatment Period â?¢ Improvement in QoL from baseline to the end of treatment Period Timepoint: Base Line and End of study which is after one year

Countries

India

Contacts

Public ContactDr VT Sriraam MBBS MD

Auroville Health Care Research and Development Private Limited

sriraamvt@aurovillehealthcare.com9840909155

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026