Status:
RECRUITING
Postoperative Pain After Full Pulpotomy With TheraCal PT, Biodentin, and MTA
Lead Sponsor:
Cumhuriyet University
Conditions:
Symptomatic Irreversible Pulpitis (SIP)
Eligibility:
All Genders
18-45 years
Phase:
NA
Brief Summary
In this study, the researchers will evaluate the effect of three highly biocompatible materials-TheraCal PT (ThPT), Biodentin, and MTA-on postoperative pain in permanent teeth affected by deep caries ...
Detailed Description
The ethical approval for our study has been obtained from the Clinical Research Ethics Committee of Sivas Cumhuriyet University. The experimental phase of the study will be conducted at the Department...
Eligibility Criteria
Inclusion
- Age range should be between 18 and 45,
- Systemic disease should be absent,
- Apical periodontitis findings may or may not be present,
- Irreversible pulpitis symptoms should be present,
- The apex of the tooth should be closed,
- Pulp sensitivity tests (cold test and electric pulp test) should respond positively,
- Periodontal pocket depth and mobility should be within normal limits,
- Rubber dam isolation should be provided for the tooth to be treated,
- Restorative treatment of the tooth should be performed,
- The patient's mouth opening should be sufficient.
Exclusion
- The patient has any systemic disease (including conditions requiring prophylaxis),
- The patient has mental or psychiatric disorders,
- The patient has any allergic condition,
- The patient has used painkillers in the last 12 hours before the procedure and antibiotics in the last week,
- There is a loss of material in an amount that cannot be restoratively treated,
- The presence of a fistula tract or abscess,
- A negative response to pulp sensitivity tests (cold test and electric pulp test),
- No bleeding in the pulp or failure to achieve hemostasis within 6 minutes after total pulpotomy,
- The apex is open,
- Advanced canal calcification is observed on periapical radiography,
- The presence of internal or external root resorption.
Key Trial Info
Start Date :
December 12 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
November 1 2025
Estimated Enrollment :
51 Patients enrolled
Trial Details
Trial ID
NCT06880471
Start Date
December 12 2024
End Date
November 1 2025
Last Update
March 17 2025
Active Locations (2)
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1
Faculty of Dentistry, Sivas Cumhuriyet University
Sivas, Turkey (Türkiye), 58000
2
Sivas Republic University Faculty of Dentistry
Sivas, Turkey (Türkiye), 58000