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Clinical Trials in Turkey / NCT07701642
Starting soon Observational

Assessment of Peridontal Inflamatuar Markers in MIH

NCT07701642 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-07-16
Last updated
2026-07-14

Condition(s) studied

Molar-Incisor Hypomineralization (MIH)

Investigational drug(s) / intervention(s)

Initial periodontal treatment

Initial periodontal treatment: DOS samples will be taken before and after treatment

Study summary

The goal of this observational study is to investigate periodontal inflammatory mediators in systemically healthy children aged 8-13 years with and without molar-incisor hypomineralization (MIH) who require initial periodontal treatment due to gingivitis.

The main questions it aims to answer are:

Are the levels of periodontal inflammatory mediators in gingival crevicular fluid different between children with MIH and those without MIH? Is the presence and severity of MIH associated with clinical periodontal parameters and dentin hypersensitivity?

Researchers will compare children with MIH to children without MIH to determine whether MIH is associated with changes in periodontal inflammatory mediator levels and periodontal clinical findings.

Eligibility

Sex
ALL
Min age
8 Years
Max age
13 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Systemically healthy children aged 8-13 years (both sexes). * Children who demonstrate adequate cooperation for dental treatment and study procedures (Frankl Behavior Rating Scale score ≥3). * Study group: Children with molar-incisor hypomineralization (MIH) affecting at least three permanent first molars and requiring initial periodontal treatment for gingivitis. * Control group: Children without molar-incisor hypomineralization who require initial periodontal treatment for gingivitis. * Presence of gingivitis requiring initial periodontal therapy. Exclusion Criteria: * Use of antibiotics within the previous 1 month. * Radiographic evidence of periodontal destruction. * History of periodontal treatment within the previous 3 months. * Presence of systemic, chronic, or metabolic diseases. * Ongoing active orthodontic treatment. * Developmental enamel defects other than molar-incisor hypomineralization. * History of premature birth.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Marmara Üniversitesi Recep Tayyip Erdoğan Külliyesi Sağlık Yerleşkesi, Diş Hekimliği Fakültesi Istanbul MALTEPE

More Marmara University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07701642 on ClinicalTrials.gov ↗ ← All trials in Turkey