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Weekly vs Daily Teriparatide Therapy in Severe Postmenopausal Osteoporosis

Primary Purpose

Osteoporosis

Status
Unknown status
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Teriparatide
Sponsored by
Postgraduate Institute of Medical Education and Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoporosis focused on measuring osteoporosis, Teriparatide

Eligibility Criteria

50 Years - 70 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Postmenopausal women of age group 50-70 having T score less than -2.5 SD or lower at lumbar spine or proximal femur.

Exclusion Criteria:

  • Patients with renal dysfunction (serum creatinine >1.5)
  • Primary and secondary hyperparathyroidism
  • Secondary osteoporosis
  • Unexplained elevated ALP (alkaline phosphatase)
  • History of therapeutic radiation
  • Active malignancy and patients having implant
  • Patients who have received i.v. or oral bisphosphonates in their disease course

Sites / Locations

  • PGIMERRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Daily Teriparatide group

Weekly Teriparatide group

Arm Description

This group will recieve 20µg of teriparatide by subcutaneous route daily at 8 pm for 1 year

This group will recieve 60µg of teriparatide by subcutaneous route weekly at 8pm on Sunday for 1 year

Outcomes

Primary Outcome Measures

BMD at Hip and lumber spine
DEXA scan(BMD at hip and lumbar spine) at baseline and at the end of 1 year
Reduction in fracture risk
Reduction in fracture risk using online FRAX tool( WHO fracture risk assessment tool) at baseline and at 1year

Secondary Outcome Measures

Full Information

First Posted
January 2, 2013
Last Updated
April 15, 2014
Sponsor
Postgraduate Institute of Medical Education and Research
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1. Study Identification

Unique Protocol Identification Number
NCT01760798
Brief Title
Weekly vs Daily Teriparatide Therapy in Severe Postmenopausal Osteoporosis
Official Title
To Compare Efficacy of Weekly Versus Daily Teriparatide in the Management of Postmenopausal Osteoporosis
Study Type
Interventional

2. Study Status

Record Verification Date
April 2014
Overall Recruitment Status
Unknown status
Study Start Date
January 2012 (undefined)
Primary Completion Date
June 2014 (Anticipated)
Study Completion Date
December 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Postgraduate Institute of Medical Education and Research

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Osteoporosis is characterized by decreased bone strength and it is prevalent among postmenopausal women but also occurs in men and women with underlying conditions or major risk factors associated with bone demineralization. Its chief clinical manifestations are vertebral and hip fractures, although fractures can occur at any skeletal site.The World Health Organization (WHO) operationally defines osteoporosis as a bone density that falls 2.5 standard deviations (SD) below the mean for young healthy adults of the same gender-also referred to as T-score of -2.5. Postmenopausal women who fall at the lower end of the young normal range (a T-score of >1 SD below the mean) are defined as having low bone density (osteopenia) and are also at increased risk of osteoporosis. More than 50% of the fractures, including hip fractures, among postmenopausal women occur in this group. Teriparatide is one of the most effective treatment options for osteoporosis. But the cost of teriparatide is prohibitively expensive and in countries like India with limited personal resources of the individuals, its not a feasible option in the majority of the patients with severe osteoporosis. The investigators aim to compare weekly versus daily teriparatide therapy in an open label non inferiority trial and if successful, the investigators anticipate, the cost of treatment could be reduced considerably so that treatment becomes more affordable to a larger number of patients. Also with weekly therapy, number of multiple injections could be brought down.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoporosis
Keywords
osteoporosis, Teriparatide

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Daily Teriparatide group
Arm Type
Active Comparator
Arm Description
This group will recieve 20µg of teriparatide by subcutaneous route daily at 8 pm for 1 year
Arm Title
Weekly Teriparatide group
Arm Type
Experimental
Arm Description
This group will recieve 60µg of teriparatide by subcutaneous route weekly at 8pm on Sunday for 1 year
Intervention Type
Drug
Intervention Name(s)
Teriparatide
Primary Outcome Measure Information:
Title
BMD at Hip and lumber spine
Description
DEXA scan(BMD at hip and lumbar spine) at baseline and at the end of 1 year
Time Frame
1 year
Title
Reduction in fracture risk
Description
Reduction in fracture risk using online FRAX tool( WHO fracture risk assessment tool) at baseline and at 1year
Time Frame
6 week, 6 month and 1 year

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Postmenopausal women of age group 50-70 having T score less than -2.5 SD or lower at lumbar spine or proximal femur. Exclusion Criteria: Patients with renal dysfunction (serum creatinine >1.5) Primary and secondary hyperparathyroidism Secondary osteoporosis Unexplained elevated ALP (alkaline phosphatase) History of therapeutic radiation Active malignancy and patients having implant Patients who have received i.v. or oral bisphosphonates in their disease course
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sanjay Kr Bhadada, DM
Email
bhadadask@rediffmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Vipin Gupta, MBBS
Email
drvipin.gupta@yahoo.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sanjay Kr Bhadada, DM
Organizational Affiliation
Associate Professor, Department of Endocrinology, PGIMER Chandigarh India
Official's Role
Principal Investigator
Facility Information:
Facility Name
PGIMER
City
Chandigarh
State/Province
UT
ZIP/Postal Code
1600012
Country
India
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sanjay Kr Bhadada, DM
Email
bhadadask@rediffmail.com
First Name & Middle Initial & Last Name & Degree
Sanjay Kr Bhadada, DM

12. IPD Sharing Statement

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Weekly vs Daily Teriparatide Therapy in Severe Postmenopausal Osteoporosis

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