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NCT05964387 · ClinicalTrials.gov registry record · NA

Effect of Silver Diamine Fluoride on Local Anesthesia in Hypomineralized Molars

A NA study of Anesthesia, Local and Molar Incisor Hypomineralization, sponsored by University of Michigan.

Recruiting
Registry status
NA
Development phase
50
Enrollment target
1
Study location

NCT05964387 is a NA study of Anesthesia, Local and Molar Incisor Hypomineralization that is actively recruiting participants, run by University of Michigan. The registered enrollment target is 50 participants, below the 80-participant average among 18 other Anesthesia, Local trials with a reported enrollment target (37% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05964387, a NA study of Anesthesia, Local and Molar Incisor Hypomineralization, is actively recruiting participants, sponsored by University of Michigan.

RECRUITING
Registry status
NA
Development phase
50 participants
Enrollment target
1
Study location

Study Summary

The purpose of this randomized, controlled clinical study is to evaluate if application of 38% SDF increases the efficacy of local anesthesia during operative dentistry on permanent molars affected by molar-incisor hypoplasia (MIH). The goal is to determine if pre-operative application of SDF results in improved local anesthesia and decrease in procedural pain in MIH affected teeth, thereby addressing an important challenge in routine clinical practice and contributing to the development of a treatment protocol for MIH affected molars.

Conditions Studied

Anesthesia, Local Molar Incisor Hypomineralization

Interventions

  • DEVICE SDF
  • DEVICE Placebo

Study Locations (1)

Michigan

  • University of Michigan - Ann Arbor

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2023-06-12
Est. Completion 2027-12-31
Phase NA

Sponsor

University of Michigan

1,327 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05964387

The ClinicalTrials.gov registry entry for NCT05964387 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 80-participant average among 18 other Anesthesia, Local trials with a reported enrollment target (37% lower). The listed sponsor is University of Michigan, which has 1,327 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Anesthesia, Local appearing as the primary indexed condition, and to 2 interventions - of which SDF is the first listed.

NCT05964387 reports 1 study location spanning 1 distinct geographic area - top geographies include Michigan.

Frequently Asked Questions

What is clinical trial NCT05964387 about?

NCT05964387 is a clinical study titled "Effect of Silver Diamine Fluoride on Local Anesthesia in Hypomineralized Molars". The purpose of this randomized, controlled clinical study is to evaluate if application of 38% SDF increases the efficacy of local anesthesia during operative dentistry on permanent molars affected by molar-incisor hypoplasia (MIH). The goal is to determine if pre-operative application of SDF result...

What is the current status of trial NCT05964387?

This trial is currently recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2023-06-12. Estimated completion is 2027-12-31.

What conditions does trial NCT05964387 study?

This clinical trial studies the following conditions: Anesthesia, Local, Molar Incisor Hypomineralization.

What interventions are being tested in trial NCT05964387?

The interventions under investigation include: SDF (DEVICE), Placebo (DEVICE).

Who is sponsoring clinical trial NCT05964387?

This trial is sponsored by University of Michigan, which has 1,327 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05964387 being conducted?

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

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.