ClinicalTrials.gg
RecruitingNCT06586996Updated Sep 19, 2024

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

An observational study in Osteoporosis Fracture, sponsored by Peking University Third Hospital. Recruiting at 1 site in China. Open to participants aged 50 Years to 100 Years. Per ClinicalTrials.gov, last updated 2024-09-19.

Sponsored by Peking University Third Hospital · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2024, 1 year 10 months ago, but the record still lists the study as recruiting.
  • Started Jan 2021; still recruiting 5 years 10 months later.

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Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
500
Ages
50 Years to 100 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 13 studies in Osteoporotic Fractures with a site in China — 7 open to participants now, 8 under way, none of them phase 3. Osteoporotic Fractures · China.

Started
2021
with 2 others
Observational
5 of 13
2 open now
Registered
11th of 13
by date
Lead sponsor
1 of 13
Peking University Third Hospital

Among the 13 studies in Osteoporotic Fractures with a site in China, this one is one of 3 that started in 2021, is one of 5 observational ones, and was the 11th registered.

Osteoporotic Fractures

87 studies on the registry are indexed under Osteoporotic Fractures; 22 are open to participants now.

Browse Osteoporotic Fractures studies →

Open to participants now

7 of the 13 studies in Osteoporotic Fractures with a site in China are open now. Recruiting first, the newest first:

1 more — sign in →

All 7 open studies →

A study can be open while its sites in China have not opened yet or have stopped. Only those recruiting at a site in China →

Who these studies take

Of the 14 Osteoporotic Fractures studies recruiting now, 9 (64%) set no upper age limit and none (0%) stop at 75 or younger; 1 takes children under 18; 2 take healthy volunteers.

This study: 50 Years to 100 Years · all sexes · no healthy volunteers.

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02

Study 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

03

Conditions studied

  • Osteoporosis Fracture

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Keywords

  • osteoporosis fracture
04

Who can participate

Ages eligible
50 Years to 100 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All the acute osteoporosis vertebral compression fracture patients who search for treatments in our hospital

Eligibility criteria

Inclusion Criteria: all patients who suffer a acute osteoporosis vertebral compression fractures -

Exclusion Criteria: those who have endocrine disease which have impacts on the bone density

-

05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
500 participants (estimated)
Patient registry
No

Groups and cohorts

  • osteoporotic vertebral compression fractures

    Other: no intervention

Interventions

  • Otherno intervention

    no intervention

06

What researchers measure

Primary outcomes

  1. VAS value

    the visual analogue scale value of patient

    Time frame: 2 weeks, 1 month, 2 months, 3months, 6 months and 12 months

  2. vertebrae height

    the height of the vertebrae according to the X rays

    Time frame: 2 weeks, 1 month, 2 months, 3months, 6 months and 12 months

  3. T value

    the T value of the dual energy X-ray absorptiometry

    Time frame: 6months and 12 months

07

Study locations

1 of 1 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jan 2021 (actual). Primary completion is estimated for Dec 2024, 47 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 4, 2024
First posted
Sep 19, 2024
StartActual
Jan 1, 2021
Primary completionEst.
Dec 31, 2024
CompletionEst.
Dec 31, 2024
Last update
Sep 19, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 19, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06586996
Responsible party
Sponsor
First posted
Sep 19, 2024
Start date
Jan 1, 2021
Primary completion
Dec 31, 2024 (estimated)
Completion
Dec 31, 2024 (estimated)
Last update
Sep 19, 2024

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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