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NCT04781517: DPROIPLDDALF

Development of a Patient-reported Outcome Instrument for Patients With Lumbar Degenerative Disease After Lumbar Fusion

Status unknown Last updated 9 February 2022
What this trial tests

trial in Lumbar Spine Degeneration in 400 participants. Status unknown.

Timeline
1 May 2020
Primary endpoint
1 March 2023
1 May 2023

Quick facts

Lead sponsorPeking University Third Hospital
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment400
Start date1 May 2020
Primary completion1 March 2023
Estimated completion1 May 2023
Sites1 location across China

Conditions studied

Sponsor

Peking University Third Hospital

Who can join

Eligibility, any sex, with Lumbar Spine Degeneration. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The commonly used scales (ODI+JOA-29+VAS) lack the assessment of lumbar stiffness, and there is no scale for evaluating lumbar stiffness in China.Based on the Delphi method and the analytic hierarchy process, this study will improve and optimize the quality of life evaluation system for patients with severe degenerative lumbar disease, so as to obtain a concise, practical, and effective patient-reported outcome instrument.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Lumbar Spine Degeneration

Currently open trials in the same condition.

Other Peking University Third Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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