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NCT03367052

Clinical and Radiological Outcomes: Two-level Cervical ProDisc-C Vivo Versus Hybrid Construct.

Status unknown NA Last updated 8 December 2017
What this trial tests

NA trial testing Two level Prodisc-C vivo in Cervical Disc Disease in 542 participants. Status unknown.

Timeline
1 January 2018
Primary endpoint
1 December 2025
1 December 2025

Quick facts

Lead sponsorPeking University People's Hospital
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment542
Start date1 January 2018
Primary completion1 December 2025
Estimated completion1 December 2025

Drugs / interventions tested

Conditions studied

Sponsor

Peking University People's Hospital

Who can join

Adults 20 to 70, any sex, with Cervical Disc Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this study is to investigate the clinical and radiological results of two-level cervical ProDisc-C vivo versus hybrid construct.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Cervical Disc Disease

Currently open trials in the same condition.

Other Peking University People's Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03367052.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing