Topical agents for vital pulpotomy in primary teeth

Phase 2

• Conditions: Dental caries; Oral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon

• Registration Number: ACTRN12619001280190
• Lead Sponsor: Damascus University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-09-17
• Last Update Posted: 30 September 2019

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Inclusion Criteria of participants:
1. Healthy and Cooperative patients approving the trial.
Inclusion Criteria of teeth:
1. Tooth is restorable.
2. Hemostasis achieved within 5 minutes during clinical procedure.
3. Presence of two-thirds of the root length radiographically.

Exclusion Criteria

1. Clinical Signs and symptoms that indicate an infected pulp: abnormal tooth mobility, sensitivity to percussion, and gingival abscess or fistula associated with a tooth.
2. Radiographic evidence of pulp degeneration: internal or external root resorption, and interradicular or periapical bone destruction.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Efficacy of Chitosan as a pulpotomy medicament in primary teeth will be assessed clinically and radiographically<br><br>[(To) Re-evaluate clinically and radiographically in three time interval stages:<br>(T1): 3 months after treatment <br>(T2): 6 months after treatment <br>(T3): 9 months after treatment <br>]

Secondary Outcome Measures

Name	Time	Method
il[Nil]