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

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

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06261762
Enrollment
20
Registered
2024-02-15
Start date
2024-02-29
Completion date
2026-06-30
Last updated
2024-02-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Wound Heal

Brief summary

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.

Interventions

None listed

Sponsors

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

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Bone level change from baselineBaseline and at 8 weeksMeasured in millimeters using segmented surface model superimpositions. Changes in bone loss between baseline and an 8 week healing period using CBCT. From the Digital Imaging and Communications in Medicine (DICOM) files two surface mesh models were generated, which were superimposed and the changes were subsequently analyzed.
Soft tissue change from baselineBaseline and at 8 weeksChanges in soft tissue loss at baseline and 8 weeks were analyzed using digital dental impressions acquired from intraoral scans, which were superimposed and the changes were analyzed.

Secondary

MeasureTime frameDescription
Correlation between baseline facial bone thickness and dimensional soft tissue alterations during healing at the interalveolar septum.Baseline and at 8 weeksTo measure correlation, the Spearman Rank Correlation Coefficient was calculated. Nonparametric models for longitudinal data were applied to analyze the impact of bone wall phenotype and healing period upon dimensional alterations.

Contacts

Primary ContactXinbo Yu
xinboyu@proton.me18019409340

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026