Actively Recruiting
Comparative Evaluation of the Clinical Outcome of Direct Pulp Capping Treatment in Permanent Molars
Led by Kafrelsheikh University · Updated on 2024-09-19
120
Participants Needed
1
Research Sites
31 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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 after being independently reviewed and approved by the Institution's Ethical Committee and is designed in accordance with CONSORT 2010. Selected patients who are between 19 and 40 years of age had undergone conservative treatment for deep caries management in their permanent teeth in the restorative and endodontic departments, faculty of dentistry, Kafrelsheikh university. The patients are then assigned randomly into four different groups for this randomized clinical study. The decision for direct pulp capping will be made after informing the patients about all the pulp capping procedures that are suggested. Furthermore, any possible complications, postoperative discomfort, or failure of the treatment will be discussed with the patient. All included patients signed a written informed consent before enrollment
CONDITIONS
Official Title
Comparative Evaluation of the Clinical Outcome of Direct Pulp Capping Treatment in Permanent Molars
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged between 19 and 40 years
- Pulp exposure due to caries removal
- Vital teeth with mild, tolerable pain associated with cold drinks
- Teeth sensitive to cold or heat with pain subsiding after stimulus removal
- Normal periapical radiographs with no signs of root resorption or radiolucency
- Exposed pulp diameter between 0.5 and 1 mm
- Patient acceptance and informed consent to participate in the study
You will not qualify if you...
- Permanent teeth with extensive caries involving more than two-thirds of dentin near the pulp
- Teeth with spontaneous pain, swelling, abscess, sinus tract, or abnormal mobility
- Teeth sensitive to pressure, percussion, or palpation indicating non-vital pulp
- Presence of radiographic signs of pathology such as root resorption or radiolucency
- Bleeding persisting longer than three minutes after pulp exposure during treatment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
kafrelsheikh University
Kafr ash Shaykh, Kafr El-Shaikh, Egypt, 33511
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
4
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here