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

Phase 4

Completed

• Conditions: Good general health and no history of systemic illness who has primary molars with deep carious lesion; Pulpotomy, Biodentine, Formocresol, Primary molar, Success rate

• Registration Number: TCTR20181115015
• Lead Sponsor: Faculty of dentistry, Mahidol university

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2017-04-07
• Study Start: 2018-11-15
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 50

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.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Success rate 6 months Percent of success rate

Secondary Outcome Measures

Name	Time	Method
/A N/A N/A