Actively Recruiting

Phase Not Applicable
Age: 18Years - 90Years
All Genders
NCT07078890

Effect of Bone Augmentation Simultaneous to Implant Removal on the Prognosis of Reimplantation at the Same Site

Led by The Dental Hospital of Zhejiang University School of Medicine · Updated on 2025-07-22

40

Participants Needed

3

Research Sites

124 weeks

Total Duration

On this page

Sponsors

T

The Dental Hospital of Zhejiang University School of Medicine

Lead Sponsor

H

Hospital of Stomatology, Wuhan University

Collaborating Sponsor

AI-Summary

What this Trial Is About

The aim of this study was to investigate the effect of bone augmentation simultaneous to implant removal on the prognosis of reimplantation at the same sites, providing recommendations for management strategies after failed implant removal.

CONDITIONS

Official Title

Effect of Bone Augmentation Simultaneous to Implant Removal on the Prognosis of Reimplantation at the Same Site

Who Can Participate

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age greater than 18 years
  • Implant failure requiring removal
  • Plan to reimplant in the same site
  • Periodontal health or stabilized periodontitis after treatment
Not Eligible

You will not qualify if you...

  • Uncontrolled metabolic diseases
  • Taking medications that affect bone metabolism
  • Implant detached at the time of consultation
  • Do not consent to reimplant in the same site
  • Unwilling to participate in follow-up
  • Other conditions that do not qualify for implant therapy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

Hospital of Stomatology, Wuhan University

Wuhan, Hubei, China, 430079

Actively Recruiting

2

The Affiliated Stomatology Hospital of Zhejiang University School of Medicine

Hangzhou, Zhejiang, China, 310000

Actively Recruiting

3

Shanghai Stomatological Hospital

Shanghai, China, 200001

Actively Recruiting

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Research Team

M

Misi Si

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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