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NCT02298504 · ClinicalTrials.gov registry record · Phase 4

Vital Pulp Treatment in Primary Teeth

A Phase 4 study of Indirect Pulp Cap and Pulpotomy, sponsored by University of Maryland, Baltimore.

Active
Registry status
Phase 4
Development phase
76
Enrollment target
1
Study location

NCT02298504: Active Phase 4 study of Indirect Pulp Cap and Pulpotomy, sponsored by University of Maryland, Baltimore.

NCT02298504 is a Phase 4 study of Indirect Pulp Cap and Pulpotomy that is active but no longer recruiting, run by University of Maryland, Baltimore. The registered enrollment target is 76 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (85% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02298504, a Phase 4 study of Indirect Pulp Cap and Pulpotomy, is active but no longer recruiting, sponsored by University of Maryland, Baltimore.

ACTIVE NOT RECRUITING
Registry status
Phase 4
Development phase
76 participants
Enrollment target
1
Study location

Study Summary

In primary teeth, decay that is near the pulp (tooth nerve)is treated with either a pulpotomy or indirect pulp treatment if the tooth is not going to be extracted A pulpotomy involves removing the top 1/2 of the pulp, placing a medication/material on the pulp, covering the remaining pulp with a cement, and the restoring the tooth. The purpose of this pilot study is to gain preliminary information regarding the success of Biodentine, MTA, and IPT in the treatment of deep decay in children's primary molars.

Primary Outcome

No signs of abscess or any swelling related to the tooth, no signs of fistula or other pathology, no signs of pathologic mobility, no post-operative pain, no pain on palpation or percussion of the tooth

Interventions

  • DRUG Mineral Trioxide Aggregate
  • DRUG Biodentin
  • DEVICE Vitrebond

Study Locations (1)

Maryland

  • University of Maryland School of Dentistry - Baltimore

Trial Details

FieldValue
Enrollment Target 76 participants
Start Date 2018-07-01
Est. Completion 2026-12-01
Phase Phase 4
University of Maryland, Baltimore

560 total trials

What the registry record for NCT02298504 still lists

NCT02298504 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 76 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (85% lower).

The record links to 3 conditions, with Indirect Pulp Cap appearing as the primary indexed condition, and to 3 interventions - of which Mineral Trioxide Aggregate is the first listed.

NCT02298504 reports a single indexed study location in Maryland.

Frequently Asked Questions

What is clinical trial NCT02298504 about?

NCT02298504 is a clinical study titled "Vital Pulp Treatment in Primary Teeth". In primary teeth, decay that is near the pulp (tooth nerve)is treated with either a pulpotomy or indirect pulp treatment if the tooth is not going to be extracted A pulpotomy involves removing the top 1/2 of the pulp, placing a medication/material on the pulp, covering the remaining pulp with a ceme...

What is the current status of trial NCT02298504?

This trial is currently active not recruiting. It is a Phase 4 study. The enrollment target is 76 participants. The study started on 2018-07-01. Estimated completion is 2026-12-01.

What conditions does trial NCT02298504 study?

This clinical trial studies the following conditions: Indirect Pulp Cap, Pulpotomy, Vital Pulp Therapies.

What interventions are being tested in trial NCT02298504?

The interventions under investigation include: Mineral Trioxide Aggregate (DRUG), Biodentin (DRUG), Vitrebond (DEVICE).

Who is sponsoring clinical trial NCT02298504?

This trial is sponsored by University of Maryland, Baltimore, which has 560 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02298504 being conducted?

This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Indirect Pulp Cap

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02298504's enrollment target sits among peer trials

76 994th of 2000 higher than 1,000 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02298504, the US trial registry maintained by the National Library of Medicine. NCT02298504 (small enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.