The Construction of Bidirectional Column Study of Acute Osteoporotic Vertebral Compression Fractures

Recruiting

• Conditions: Osteoporosis Fracture
• Interventions: Other: no intervention

• Registration Number: NCT06586996
• Lead Sponsor: Peking University Third Hospital

Brief Summary

Our research group plans to establish a disease specific bidirectional cohort study on prognosis prediction of acute osteoporotic vertebral compression fracture based on imaging and clinical data, and to establish a comprehensive bioinformation database on OVCFs, including patient status, clinical data, laboratory examination, and imaging examination database

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2021-01-01
• Status Verified: 2024-01
• Study First Submitted: 2024-09-04
• Study First Submitted QC: 2024-09-04
• Last Update Submitted: 2024-09-04
• Study First Posted: 2024-09-06
• Last Update Posted: 2024-09-06
• Primary Completion: 2024-12-31
• Study Completion: 2024-12-31

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 500

Inclusion Criteria

all patients who suffer a acute osteoporosis vertebral compression fractures -

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Exclusion Criteria

those who have endocrine disease which have impacts on the bone density

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
osteoporotic vertebral compression fractures	no intervention	-

Primary Outcome Measures

Name	Time	Method
VAS value	2 weeks, 1 month, 2 months, 3months, 6 months and 12 months	the visual analogue scale value of patient
vertebrae height	2 weeks, 1 month, 2 months, 3months, 6 months and 12 months	the height of the vertebrae according to the X rays
T value	6months and 12 months	the T value of the dual energy X-ray absorptiometry

Trial Locations

Locations (1)

Peking University Third Hospita; 🇨🇳 Beijing, China