Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
NCT05188196

Efficacy of Collagen Sponge Versus Collagen Membrane on Ridge Preservation of Periodontally Compromised Teeth

Led by The Dental Hospital of Zhejiang University School of Medicine · Updated on 2024-08-07

36

Participants Needed

1

Research Sites

208 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The study aims to evaluate the efficacy of ridge preservation with collagen sponge or collagen membrane in combination with collagenated bovine bone mineral in extraction sockets of periodontally diseased teeth.

CONDITIONS

Official Title

Efficacy of Collagen Sponge Versus Collagen Membrane on Ridge Preservation of Periodontally Compromised Teeth

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Need for molar extraction due to periodontal disease with plan for late implantation
  • No acute infection such as abscess or effusion
  • Presence of bone defects on one or two socket walls with horizontal component greater than 50% of root length and socket wall height at least 3 mm
  • Presence of one adjacent tooth to the extraction site
Not Eligible

You will not qualify if you...

  • Smoking
  • Pregnancy or lactation
  • Untreated periodontal disease
  • Severe systemic conditions that contraindicate surgery such as diabetes, heart disease, or cancer
  • Undergoing radiotherapy
  • Systemic disease or medications affecting bone metabolism and mucosal healing, including immunosuppressants, phenytoin, bisphosphonates
  • Extraction of multiple adjacent teeth
  • Allergy to any materials used in the study

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

The Affiliated Stomatology Hospital of Zhejiang University School of Medicine

Hangzhou, Zhejiang, China

Actively Recruiting

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Research Team

W

Weida Li, master

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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