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Comparison of the Efficacy between Coronal Pulpotomy and Pulpectomy in the Treatment of Irreversible Coronal Pulpitis in Primary Teeth

Comparison of the Efficacy between Coronal Pulpotomy and Pulpectomy in the Treatment of Irreversible Coronal Pulpitis in Primary Teeth

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108545
Enrollment
Unknown
Registered
2025-09-01
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Irreversible Pulpitis in Primary Teeth

Interventions

Experimental Group:Coronal Pulpotomy
Control Group:Pulpectomy

Sponsors

Stomatological Hospital Affiliated to Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 8 Years

Inclusion criteria

Inclusion criteria: 1. Children aged 3-8 years; 2. Preoperative diagnosis of irreducible pulpitis of deciduous teeth; 3. No percussion pain, abnormal looseness, no soft tissue swelling or fistula; 4. Preoperative imaging examination showed no periapical lesion and internal and external resorption; 5. After removing the top, the coronary pulp tissue can be formed; 6. After removing the coronary medull, the pulp at the pulp-like root canal mouth has a tough texture and healthy color, and hemostasis can be obtained within 1-10 minutes.

Exclusion criteria

Exclusion criteria: 1. Suffering from systemic diseases or mental illnesses; 2. Allergy to anesthetic drugs or therapeutic materials; 3. Percussion pain, abnormal looseness, soft tissue swelling or fistula, etc.; 4. Abnormal root development, physiological resorption > 1/3 of the root, or abnormal development of permanent tooth germ; 5. X-ray shows apical transmission or pathological root resorption; 6. Poor compliance and inability to cooperate with the completion of necessary clinical examination or treatment; 7. Guardians are unable to commit to regular follow-up visits, or refuse to sign informed consent.

Design outcomes

Primary

MeasureTime frame
Radiological Success Rates;Pain Relief Status;

Secondary

MeasureTime frame
operation time;

Countries

China

Contacts

Public ContactXiaoyan Hu

Stomatological Hospital Affiliated to Anhui Medical University

273640765@qq.com+86 139 0569 2530

Outcome results

None listed

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