Skip to content

The effect of brace on osteoporosis and kyphosis reduction

Evaluation of the effect of dynamic hyperextension brace on osteoporosis and kyphosis reduction in postmenopausal osteoporotic women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016111430871N2
Enrollment
60
Registered
2016-12-13
Start date
2017-03-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Condition 1: Osteoporosis. Condition 2: Kyphosis. Postmenopausal osteoporosis Postural kyphosis

Interventions

Intervention 1: Case group: A 600000 unit intramuscular vitamin D will be administered. A dose of 35 mg/ week oral Alendronate (Ostomeod, Modava Company, Iran) will also be administered as the osteopo
Treatment - Devices
Treatment - Drugs
Case group: A 600000 unit intramuscular vitamin D will be administered. A dose of 35 mg/ week oral Alendronate (Ostomeod, Modava Company, Iran) will also be administered as the osteoporosis drug of ch
Control group: A 600000 unit intramuscular vitamin D will be administered. A dose of 35 mg/ week oral Alendronate (Ostomeod, Modava Company, Iran) will also be administered as the osteoporosis drug of

Sponsors

Vice chancellor for research, Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: Female; postmenopausal; osteoporosis; Kyphosis; Exclusion criteria: Patients having metabolic or hormonal disorders affecting the skeletal structure; patients receiving drugs with known affect on bone metabolism; patients currently receiving osteoporosis treatment; patients not able to use brace;

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Osteoporosis. Timepoint: At the start of the study and one year after the start of the intervention. Method of measurement: Bone mineral density.;Kyphosis. Timepoint: At the start of the study and one year after the start of the intervention. Method of measurement: Ruler.

Secondary

MeasureTime frame
-. Timepoint: -. Method of measurement: -.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Mirzaei

Bone & Joint Reconstraction Research Center

mirzaeialireza26@gmail.com+98 21 3354 2000

Outcome results

None listed

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