CompletedNot Applicable

Pulpotomy Versus Pulpectomy in Vital Primary Incisors

39 participantsStarted 2015-08-01

Plain-language summary

The aim of this split mouth randomized controlled study was to compare formocresol pulpotomy and zinc-oxide and eugenol pulpectomy in the treatment of vital pulp exposure in primary incisor. 39 Contralateral pairs of incisors were randomly assigned to receive pulpotomy or pulpectomy in children aged from 18 to 66 months old. Clinical and radiographical evaluations were performed at 6 and 12 months

Who can participate

Age range

18 Months – 7 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: * Two or more carious vital primary maxillary incisors where exposure of the vital pulp following the removal of dental caries was inevitable. * No history of spontaneous pain * No lingering provoked pain * No pain on percussion, No fistula, or sinus tract * No history of trauma * No periapical radiolucency * No pathologic root resorption * No pulp calcification. Exclusion Criteria: * Teeth with physiologic resorption exceeding one-third of the root * Teeth non-restorable with crowns.

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 failure

Timeframe: 1 year

radiographic failure

Timeframe: 1 year

Trial details

NCT IDNCT05589025

SponsorNational Research Centre, Egypt

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2016-12-01

View on ClinicalTrials.gov More Dental Caries trials