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Vital pulp therapy by decompressed filling technique in irreversible pulpitis

Vital pulp therapy by decompressed filling technique in irreversible pulpitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900028086
Enrollment
Unknown
Registered
2019-12-11
Start date
2019-12-16
Completion date
Unknown
Last updated
2019-12-16

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

Conditions

irreversible pulpitis

Interventions

Case series:decompressed filling technique

Sponsors

Beijing Stomatological Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Voluntarily participate the clinical trial and sign the informed consent form; Aged 18 to 70 years old; 2. Clinical examination reveals deep caries or secondary deep caries in the crown of the tooth; 3. No symptoms of the tooth, or had occasionally cold stimulation sensitivity, may had a history of spontaneous pain; 4. Cold test of the tooth shows normal, or the pain caused by the cold stimulation does not last more than 2 mins; 5. Percussion of the tooth shows normal or uncomfortable; 6. The tooth does not loosen; 7. X-ray and CBCT images show radiolucency near or reaching the pulp cavity in the crown. There was no radiolucency around the apical apex or slight enlargement exists in periapical membranes; 8. During the treatment procedure, the pulp does not expose until all decayed lesions are removed. The formed pulp tissue was observed under the microscope. The pulp was not completely liquefied and necrotic. The pulp bleeds after pulp exposure, after 5 mins, no active bleeding occurred.

Exclusion criteria

Exclusion criteria: 1. Serious systemic and organic diseases; 2. Cracks exist across the marginal ridge in crown, vertical root fracture or occlusal trauma existed; 3. Hot test shows severe pain; 4. Poor oral hygiene, the gum of the tooth is red and swollen, bleeding occurs after periodontal probing, the depth of periodontal pocket>4mm, combined periodontal-endodontic lesions exist; 5. Periapical lesion, internal or external root resorption can be observed in X-ray and CBCT images; 6. Patients had taken antibiotics within 4 weeks; 7. Patients who prepare to pregnant, during pregnancy, or being lactation; patients with systemic disease or have long-term medication history; 8. During the treatment, the edges of the tooth are located under the gingiva after the decayed lesions removed; when collecting the exudate of the pulp, cannot avoid the contamination of gingival crevicular fluid, saliva or gingival bleeding; 9. Cannot return to the hospital attend the follow-up on time; 10. The researchers believe that any situation that are not suitable for participation.

Design outcomes

Primary

MeasureTime frame
electric pulp test;periapical tissue;clinical exam;

Countries

China

Contacts

Public ContactYing Zheng

Beijing Stomatological Hospital, Capital Medical University

zhengyingyus@163.com+86 15811562452

Outcome results

None listed

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