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NCT06614296

Unscheduled Hospital Readmission After Crenel Lateral Interbody Fusion

Completed Last updated 1 October 2024
What this trial tests

trial testing Crenel Lateral Interbody Fusion in Spine Degeneration in 100 participants. Completed in 2 August 2024.

Timeline
3 April 2024
Primary endpoint
25 July 2024
2 August 2024

Quick facts

Lead sponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment100
Start date3 April 2024
Primary completion25 July 2024
Estimated completion2 August 2024
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Second Affiliated Hospital, School of Medicine, Zhejiang University

Who can join

18 and older, any sex, with Spine Degeneration. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this observational study is to learn about the readmission related to Crenel Lateral Interbody Fusion (CLIF). The main question it aims to answer is: What are the risk factors for readmission after CLIF surgery?

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Spine Degeneration

Currently open trials in the same condition.

Other Second Affiliated Hospital, School of Medicine, Zhejiang University trials

Trials by the same sponsor.

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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/NCT06614296.

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