UnknownNot Applicable

Assessment of Vital Pulp Therapy in Permanent Molars

Turkey (Türkiye)300 participantsStarted 2017-11-01

Plain-language summary

The purpose of this study is to evaluate the long term clinical performance of vital pulp therapy of young permanent teeth with irreversible pulpitis

Who can participate

Age range

6 Years – 18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients and parents of the patients who accept to participate and sign the informed consent * Patients who have at least one vital permanent molar teeth with irreversible pulpitis symptoms * Teeth which can be restorable after the treatment. * Teeth which has good periodontal health and in the absence of sinus tracts or swelling. Exclusion Criteria: * Patients and parents of the patients who does not accept to participate and sign the informed consent * Teeth which have dentoalveolar or extraoral swelling * Teeth which have periodontal disease, mobility or alveolar bone loss * Teeth which are not restorable * Patients who are not cooperative with the treatment

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Clinical evaluation of vital pulp therapy in permanent teeth with irreversible pulpitis

Timeframe: 3 years

Trial details

NCT IDNCT03410134

SponsorHacettepe University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-08-01

Contact for this trial

Zafer C Cehreli, Prof

00905353197969 zcehreli@gmail.com

View on ClinicalTrials.gov More Dental Caries Extending to Pulp trials

Who can participate

Age range

6 Years – 18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.