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Clinical research of using iROOT BP PLUS in partial pulpotomy

Clinical research of using iROOT BP PLUS in partial pulpotomy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-17010806
Enrollment
Unknown
Registered
2017-03-07
Start date
2017-05-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Pulp exposure

Interventions

Experimental group:using iROOT BP PLUS in partial pulpotomy

Sponsors

School and Hospital of Stomatology, Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 18 Years

Inclusion criteria

Inclusion criteria: Pulp exposure in 24 hours by crown fracure.

Exclusion criteria

Exclusion criteria: 1. Some systemic disease; 2. Can not cooperate with treatment.

Design outcomes

Primary

MeasureTime frame
Tooth color;—

Countries

China

Contacts

Public ContactMingwen Liu

School and Hospital of Stomatology, Wuhan University

coolliumingwen@163.com+86 13986231285

Outcome results

None listed

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