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Analysis of the efficacy of posterior (occlusal) veneer in the treatment of living pulp cracked teeth

Analysis of the efficacy of posterior (occlusal) veneer in the treatment of living pulp cracked teeth

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200058630
Enrollment
Unknown
Registered
2022-04-12
Start date
2022-04-07
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Cracked teeth

Interventions

Group 1:3M Lava Ultimate occlusal veneers
Group 2:The resin is filled after grinding the cracks
Group 3:Lower post-occlusal observation

Sponsors

Department of Endodontology, Nanjing Stomatological Hospital, Medical School of Nanjing University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18-65 years; 2. The crown was intact, at least one premolar or molar (except for the third molar) has at least one crack; 3. Pulp activity is normal or transient sensitive that resolve with zinc oxide sedative treatment; 4.There was no deep periodontal pocket; 5.X-ray showed no obvious abnormalities around the apical region, no widening of the periodontal ligment or low-density images around the apical region.

Exclusion criteria

Exclusion criteria: 1. Patients whose teeth are too tightly occluded to prepare enough space; 2. Patients whose imaging examination shows the following conditions: 1) Low density shadow in apical region; 2) Alveolar bone resorption was more than 1/3; 3) The affected teeth have been treated with root canal therapy; 3. Patients with bruxism; 4. Patients with xerostomia or abnormal salivary secretion; 5. Patients with a history of radiotherapy; 6. Patients with cracked teeth accompanied by enamel mineralization imperfection, dental fluorosis or tetracycline teeth; 7. Patients with uncontrollable periodontal disease or cracked teeth with depth of exploration>5mm; 8. Female patients during pregnancy or lactation; 9. Patients with uncontrolled serious systemic diseases; 10. Patients who cannot maintain oral hygiene independently; 11. After careful consideration, the patient is unwilling to repair in this way.

Design outcomes

Primary

MeasureTime frame
Treatment success rate;

Secondary

MeasureTime frame
VAS pain score;Evaluation of the restoration;incidence of adverse reactions;

Countries

China

Contacts

Public ContactYang Weidong

Department of Endodontology, Nanjing Stomatological Hospital, Medical School of Nanjing University

liutingvsvitas@126.com+86 13815891275

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026