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Clinical and Radiographic Evaluation of Pulpectomy in Primary Molars with a Modified Paste, Zinc Oxide-Eugenol, and Vitapex

Clinical and Radiographic Evaluation of Pulpectomy in Primary Molars with a Modified Paste, Zinc Oxide-Eugenol, and Vitapex

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004938
Enrollment
Unknown
Registered
2014-07-04
Start date
2012-07-01
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

pulpitis in primary teeth

Interventions

Modified Paste group:root filling with Modified Paste vs other two groups

Sponsors

Peking University School and Hospital of Stomatology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 9 Years

Inclusion criteria

Inclusion criteria: 1.Clinical characteristics, defined as spontaneous pain and the presence of a deep carious lesion with pulp exposure and bleeding that did not halt within five minutes following removal of the coronal pulp tissue;2.Radiographic evaluation revealing that the molar had no furcal or periapical radiolucencies and that physiological root resorption was less than 1/3.

Exclusion criteria

Exclusion criteria: Candidates were excluded if their molar could not be restored or if they had gingival abscesses or fistula openings.

Design outcomes

Primary

MeasureTime frame
success rate;

Secondary

MeasureTime frame
degradation rate;

Countries

China

Contacts

Public ContactXiaoxian Chen
chenxiaox2007@126.com+86 010-58595066

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 8, 2026