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The Impact of the Adequacy of Keratinized Mucosa on Peri-implant Tissue Health and Patient-reported Outcomes

T

The Dental Hospital of Zhejiang University School of Medicine

Status

Enrolling

Conditions

Edentulous Alveolar Ridge

Treatments

Other: No intervention

Study type

Observational

Funder types

Other

Identifiers

NCT07124416
2025-104

Details and patient eligibility

About

This study aims to conduct a cross-sectional study to compare the differences in clinical indices, patient-reported outcomes, and levels of inflammatory factors in peri-implant gingival crevicular fluid between sites with adequate (≥ 2 mm) and inadequate (< 2 mm) keratinized mucosa after implant restoration, in order to explore the impact of the presence of keratinized mucosa on peri-implant soft and hard tissue health.

Enrollment

150 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Individuals aged 18 to 70 years (inclusive of 18 and 70 years), of any gender;
  • Patients who have undergone dental implant restoration是(single crown or fixed bridge restorations) at the Stomatology Hospital, Zhejiang University School of medicine and have had their final restoration for at least 6 months;
  • Patients who voluntarily participate and sign the informed consent form after being fully informed, and who cooperate with relevant examinations.

Exclusion criteria

  • Patients who are unwilling to participate in the follow-up of this study for various reasons

Trial design

150 participants in 2 patient groups

inadequate keratinized mucosa
Description:
peri-implant width of keratinized mucosa less than 2 mm
adequate keratinized mucosa
Description:
peri-implant width of keratinized mucosa ≥ 2 mm
Treatment:
Other: No intervention

Trial contacts and locations

1

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Central trial contact

Misi Si

Data sourced from clinicaltrials.gov

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