MedTrace Logo

Post-Market Clinical Follow-up Study of A-SPINE's Products

NCT04848376 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2021-04-19

No results posted yet for this study

Summary

This is a post-market clinical follow-up study that use questionnaires such as Visual Analog Scale (VAS), the Neck Disability Index (NDI), or the Oswestry Disability Index (ODI) to compare the clinical improvement effects before and after surgery.

Conditions

  • Degenerative Disc Disease
  • Kyphosis
  • Scoliosis
  • Trauma
  • Tumor
  • Stenosis
  • Pseudoarthrosis of Spine
  • Deformity

Interventions

DEVICE

(1) SmartLoc (2) SmartLoc Evo (3) Winloc(4) Vigor PEEK Cervical Disc Spacer (5) Combo C (6) Polymer Lumbar Disc Spacer (7) X'Plo (8) Rainboo (9) Combo L

As long as there are patients using the above device, conduct questionnaire interview.

Sponsors & Collaborators

  • A-Spine Asia Co., Ltd.

    lead INDUSTRY

Principal Investigators

  • Bryan Huang, MD · Taichung Tzu Chi Hospital

Eligibility

Min Age
20 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-09
Primary Completion
2022-09-08
Completion
2022-09-08

Countries

  • Taiwan

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04848376 on ClinicalTrials.gov