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NCT07504614

Pre-etched Bioactive Versus Resin- Based Fissure Sealant for Permanent Molars Affected With Molar Incisor Hypomineralization (MIH): a Randomized Clinical Trial

ENROLLING BY INVITATION NA Last updated 1 April 2026
What this trial tests

NA trial testing Pre-etched Bioactive Sealant in Molar Incisor Hypomineralization in 76 participants. Enrolling by invitation.

Timeline
1 August 2025
Primary endpoint
30 August 2027
30 August 2027

Quick facts

Lead sponsorJordan University of Science and Technology
PhaseNA
StatusENROLLING BY INVITATION
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposeprevention
Enrollment76
Start date1 August 2025
Primary completion30 August 2027
Estimated completion30 August 2027
Sites1 location across Jordan

Drugs / interventions tested

Conditions studied

Sponsor

Jordan University of Science and Technology

Who can join

Adults 6 to 12, any sex, with Molar Incisor Hypomineralization or Fissure Sealant. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study aims to evaluate and compare the clinical performance of pre-etched bioactive fissure sealants to conventional RBFS in permanent molars affected by MIH in terms of retention, marginal integrity, caries prevention effect, and sensitivity.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Molar Incisor Hypomineralization

Currently open trials in the same condition.

Other Jordan University of Science and Technology trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07504614.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing