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vital pulp therapy in cariously exposed permanent teeth: a randomized controlled trial

vital pulp therapy in cariously exposed permanent teeth: a randomized controlled trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100042113
Enrollment
Unknown
Registered
2021-01-14
Start date
2021-01-01
Completion date
Unknown
Last updated
2021-04-12

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

Conditions

pulpitis

Interventions

experimental group:vital pulp therapy

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Mature or immature permanent teeth, teeth with deep caries near the pulp; 2) With or without history of spontaneous pain, prolonged pain from cold and heat stimulation, and radiation pain 3) The cold test and electrical pulp test shows vital pulp; 4) X-ray film shows that the caries reaches inner quarter of the dentin or penetrate the entire thickness of the dentin), no radiolucency at the periapical or furcation regions,the absence of calcification and obliteration of pulp canal, no internal root resorption, and external root resorption; 5) Normal periodontal tissue or 1 stage periodontitis (AL <= 2,PD <= 4); 6) The general condition is good and no other systemic diseases; 7) Had no abnormal tooth mobility and clinical swelling, No sinus tracts or swelling 8)agree to attend for recall appointment.

Exclusion criteria

Exclusion criteria: 1) The tooth is non-restorable; 2) Pregnant women or those who cannot cooperate to complete the test; 3) No pulp exposure after caries excavation; 4) Bleeding could not be controlled or the wound appears necrotic, judged by the absence of bleeding or the presence of pale necrotic pulp tissue.

Design outcomes

Primary

MeasureTime frame
Dental pulp vitality;

Countries

China

Contacts

Public ContactLiu Yuebo

Peking Union Medical College Hospital (Dongdan Campus)

1103796706@qq.com+86 18500167151

Outcome results

None listed

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