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Clinical Trials/TCTR20181115015
TCTR20181115015
Completed
Phase 4

The comparison of clinical and radiographic success between BiodentineTM and Formocresol pulpotomy in primary molars

Faculty of dentistry, Mahidol university0 sites50 target enrollmentNovember 15, 2018

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Good general health and no history of systemic illness who has primary molars with deep carious lesion
Sponsor
Faculty of dentistry, Mahidol university
Enrollment
50
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 15, 2018
End Date
April 7, 2017
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Faculty of dentistry, Mahidol university

Eligibility Criteria

Inclusion Criteria

  • \- Good general health and no history of systemic illness
  • \- Primary molars with deep carious lesion
  • \- If patient has a history of pain, the pain should be only intermittent or pain due to a stimulus such as pain when chewing food or food stuck in the decayed teeth
  • \- No clinical evidence of irreversible pulpitis or pulp necrosis such as pulp exposure, swelling of soft tissue or fistula and sinus track, abnormal tooth mobility.
  • \- No radiographic evidence of irreversible pulpits or pulp necrosis such as internal resorption, inter\-radicular bone destruction and pithily at periodical area.
  • \- Roots remain more than 2/3 of normal root length

Exclusion Criteria

  • \- The tooth has unrestorable crown
  • \- After removed caries completed. Find that caries isn’t exposed pulp
  • \- After removed the coronal pulp, hemostasis isn’t obtained by moistened cotton pellets due to the inflammation extended into radicular pulp or the pulp is necrosis.

Outcomes

Primary Outcomes

Not specified

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