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Clinical efficacy study of C-Root BP in pulpotomy of deciduous teeth

Clinical efficacy study of C-Root BP in pulpotomy of deciduous teeth

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098970
Enrollment
Unknown
Registered
2025-03-17
Start date
2025-03-18
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

Primary teeth are deeply decayed

Interventions

Test group:C-Root BP
Control group:iRoot BP Plus

Sponsors

Peking University Hospital of Stomatology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 8 Years

Inclusion criteria

Inclusion criteria: 1. Children aged 2.5-6 undergoing dental treatment under general anesthesia; 2. Asymptomatic deciduous teeth, preoperative examination shows caries origin with exposed pulp; 3. No percussion pain, abnormal looseness, no soft tissue swelling or fistula; 4. Preoperative imaging examination showed that caries had reached the entire dentin layer, without pulp or periapical diseases (including no internal absorption, external absorption, perforation, periapical or root bifurcation lesions); 5. After removing the pulp chamber top, the formed coronal pulp tissue can be seen; 6. Perform pulpotomy on the affected tooth and use prefabricated crowns for restoration; 7. No systemic or psychiatric disorders. Each child is included in one affected tooth;

Exclusion criteria

Exclusion criteria: 1. Age>6 years old, or physiological resorption of the tooth root, estimated tooth replacement within 2 years; 2. The affected tooth has symptoms such as spontaneous pain and nighttime pain; Preoperative imaging examination shows absorption inside and outside the tooth root, or root bifurcation lesions; 3. Patients who still experience bleeding after being compressed with cotton balls for more than 5 minutes after removing the coronal pulp; 4. Those who cannot follow up regularly; 5. Guardian refuses to sign informed consent form;

Design outcomes

Primary

MeasureTime frame
Success rate;

Countries

China

Contacts

Public ContactWeiqian Jia

Peking University Hospital of Stomatology

jwqsss@126.com+86 10 82195361

Outcome results

None listed

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