Hard and Soft Tissue Dimensional Change After Consecutive Extractions and Unassisted Socket Healing in the Esthetic Zone

NCT ID: NCT06261762

Last Updated: 2024-02-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

20 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-02-29

Study Completion Date

2026-06-30

Brief Summary

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The goal of this observational study is to evaluate the post-extraction hard and soft tissue dimension changes in patients requiring consecutive extractions and unassisted socket healing in the anterior maxilla. The main questions it aims to answer are:

* Is significant alveolar ridge resorption observed at center sites after consecutive extractions
* Is significant alveolar ridge resorption observed at the interalveolar septum after consecutive extractions, are different extraction sites associated with significantly different bone resorption
* Is a thick or thin wall phenotype associated with the amount of bone resorption
* Is soft tissue thickness change associated with the corresponding location (extraction site or interalveolar septum) and post-extraction thickness of the bone
* Is the interdental papilla height significantly affected after extractions.

Participants will undergo consecutive (two) extractions and will be evaluated after subsequent unassisted socket healing for 8 weeks.

Detailed Description

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Conditions

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Wound Heal

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* 18+ years old
* Require consecutive (two) teeth replacement in the anterior maxilla
* Signed informed consent
* No significant medical conditions
* Patients with healthy periodontal conditions or previously treated to controlled and stable conditions

Exclusion Criteria

* General medical (American Society of Anesthesiologists, ASA, class III or IV) and/or psychiatric contraindications
* Pregnancy or nursing
* Any interfering medication such as steroid therapy or bisphosphonate therapy
* Uncontrolled diabetes
* Autoimmune diseases or inflammatory diseases affecting the intraoral tissues
* Radiation therapy to head or neck region
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Feng Wang

Role: PRINCIPAL_INVESTIGATOR

Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University

Central Contacts

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Xinbo Yu

Role: CONTACT

18019409340

Other Identifiers

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SDC-24-1

Identifier Type: -

Identifier Source: org_study_id

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