Status:
RECRUITING
Comparative Evaluation of the Clinical Outcome of Direct Pulp Capping Treatment in Permanent Molars
Lead Sponsor:
Kafrelsheikh University
Conditions:
Vital Pulp Therapy
Eligibility:
All Genders
19-40 years
Phase:
NA
Brief Summary
This clinical trial will be performed during June 2024 and December 2024. The study is conducted following the Declaration of Helsinki Ethical principles for medical research involving human subjects ...
Detailed Description
A total of 120 posterior teeth from 60 patients are randomly divided into 4 groups according to the type of treatment; RetroMTA Conventional group, TheraCal Conventional group, RetroMTA laser group, a...
Eligibility Criteria
Inclusion
- In all patients, the pulp had been exposed because of caries removal. Data collection included clinical pulp capping respecting the following criteria.
Exclusion
- Individuals who are 19 to 40 years old.
- Permanent teeth that have not been repaired and have extensive caries on their occlusal and proximal surfaces, extending more than two-thirds of the dentin near the pulp.
- Vital teeth; asymptomatic teeth (not sensitive to pressure, percussion, or palpation, and no spontaneous pain); sinus tract devoid of swelling and abscess; abnormal mobility absent; no history of spontaneous pain; mild, dull, and tolerable pain associated with eating and drinking cold drinks.
- Ethyl chloride cold tests, gutta-percha heat testing, palpation, percussion, and the lack of radiological symptoms in periapical radiographs are used to assess the life of the teeth prior to treatment. After the stimulus is removed, pain from a pulp test that is triggered by either heat or cold should subside.
- In periapical radiography, none of the following conditions should be present: normal lamina dura and periodontal ligaments, no internal or external root resorption, and no radiolucency in the furcation area or periapical region.
- The exposed area's diameter ranges from 0.5 to 1 mm.
- Participants' acceptance of the research program.
Key Trial Info
Start Date :
June 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
January 10 2025
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT06599814
Start Date
June 1 2024
End Date
January 10 2025
Last Update
September 19 2024
Active Locations (1)
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1
kafrelsheikh University
Kafr ash Shaykh, Kafr El-Shaikh, Egypt, 33511