Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
NCT06029764

Extended One-level Interbody Fusion for Adjacent Vacuum Phenomenon in Lumbar Degenerative Disc Disease

Led by Xuanwu Hospital, Beijing · Updated on 2023-09-08

126

Participants Needed

1

Research Sites

308 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The main objective of this study was to validate the clinical effectiveness of interbody fusion with a one-segment extension for the treatment of adjacent segmental space discs in the surgical treatment of lumbar degeneration.

CONDITIONS

Official Title

Extended One-level Interbody Fusion for Adjacent Vacuum Phenomenon in Lumbar Degenerative Disc Disease

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 60 years old
  • Lumbar degeneration requiring 1-2 segment interbody fusion
  • Vacuum signs in adjacent discs without symptoms or instability (power position slip  3mm and segmental angle change  106)
  • Agreement with surgical plan and willingness for long-term follow-up
  • Signed informed consent form
Not Eligible

You will not qualify if you...

  • Drug or alcohol abuse
  • Abnormal liver or kidney function unsuitable for surgery
  • Cardiac insufficiency unsuitable for surgery
  • Severe metabolic or endocrine diseases unsuitable for surgery
  • Severe lung disorders such as asthma or abnormal lung function unsuitable for surgery
  • Pregnant, breastfeeding, or planning pregnancy soon
  • Participation in other clinical trials within 3 months
  • Considered unsuitable for the study by the investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Xuanwu Hospital, Capital Medical University

Beijing, Beijing Municipality, China

Actively Recruiting

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Research Team

H

Hao Wu, MD,PhD

CONTACT

F

Fengzeng Jian, MD,PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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