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New treatment option for Vital Pulp Therapy
Official title Comparative Evaluation of the Clinical Outcome of Direct Pulp Capping Treatment in Permanent Molars
ClinicalTrials.gov ID: NCT06599814
What this study is testing
- What it's testing
- 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.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 19 to 40. Healthy volunteers may be eligible.
You may be able to join if
- In all patients, the pulp had been exposed because of caries removal. Data collection included clinical pulp capping respecting the following...
You likely can't join if
- 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...
- Vital teeth; asymptomatic teeth (not sensitive to pressure, percussion, or palpation, and no spontaneous pain); sinus tract devoid of swelling and...
- Ethyl chloride cold tests, gutta-percha heat testing, palpation, percussion, and the lack of radiological symptoms in periapical radiographs are used...
- In periapical radiography, none of the following conditions should be present: normal lamina dura and periodontal ligaments, no internal or external...
- The exposed area's diameter ranges from 0.5 to 1 mm.
See the full eligibility criteria
- In all patients, the pulp had been exposed because of caries removal. Data collection included clinical pulp capping respecting the following criteria.
- 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...
- 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...
- 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...
- The exposed area's diameter ranges from 0.5 to 1 mm.
- Participants' acceptance of the research program.
The study team makes the final eligibility decision.
Where it's taking place
- Kafr ash Shaykh, Kafr El-Shaikh, Egypt
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 19 years to 40 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Kafr ash Shaykh, Kafr El-Shaikh, Egypt. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.