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Clinical Application Research of the Oral Scanning Pneumatic Gingival Retraction Device

Clinical Application Research of the Oral Scanning Pneumatic Gingival Retraction Device

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098214
Enrollment
Unknown
Registered
2025-03-04
Start date
2025-03-10
Completion date
Unknown
Last updated
2025-03-10

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

Conditions

Tooth defect

Interventions

Test Group 1:Pneumatic gingival discharge (PGR-S), gingival line discharge
Test group 2:Pneumatic gingival discharge (PGR-S), gingival line discharge

Sponsors

Peking University School and Hospital of Stomatology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: Experiment 1: 1)Aged 18-30 years; 2)Categorized by gingival biotype: 15 cases of thin gingival biotype and 15 cases of thick gingival biotype; 3)No active oral disease treatment, normal occlusal relationship, complete dentition; 4)Absence of hard tissue pathologies in teeth #11, #26, #46, and mandibular dentition; 5)No bleeding on probing, probing depth =6 months prior to study. Experiment 2: 1)Maxillary anterior teeth with coronal defects restored using digitally fabricated all-ceramic single crowns; 2)Preparation margins placed subgingivally at 0.5 mm with a width of 0.5–1 mm; 3)No missing natural teeth in the entire dentition; 4)Patients of any gender, with normal mouth opening, permanent dentition, good periodontal health, and no systemic complications; 5)Stratified by gingival biotype: 15 cases with thin biotype and 15 cases with thick biotype.

Exclusion criteria

Exclusion criteria: Experiment 1: 1)Restricted mouth opening impeding intraoral scanning or conventional impression taking; 2)Presence of untreated periodontal disease; 3)Long-term use of corticosteroids/immunosuppressants/aspirin/anticoagulants/other systemic medications; 4)Pregnancy. Experiment 2: Restricted mouth opening; Edentulism;Non-permanent dentition;Poor periodontal health;Severe systemic diseases;Declined study participation

Design outcomes

Primary

MeasureTime frame
Experiment 1 Gingival retraction measurement;Experiment 2 Gingival retraction measurement;

Secondary

MeasureTime frame
Experiment 1 Time;Experiment 1 Visual Rating Scale (VRS);Experiment 2 Time;Experiment 2 Visual Rating Scale (VRS);

Countries

China

Contacts

Public ContactZhongning Liu

Peking University School and Hospital of Stomatology

liuzhongning@bjmu.edu.cn+86 158 1058 3283

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026