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A comparison review of 6-month durability of hydrophilic fissure sealant and Flowable composite

A comparison review of 6-month durability of hydrophilic fissure sealant and Flowable composite in upper permanent first molar teeth of children aged 6 to 12 years.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240512061762N1
Enrollment
30
Registered
2024-06-19
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Durability of hydrophilic fissure sealant and Flowable composite.

Interventions

Intervention 1: Intervention group: Hydrophilic fissure sealant is placed on the occlusal surface of the right permanent first molar teeth. In patients after six months, the durability of the sealants

Sponsors

Sanandaj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 12 Years

Inclusion criteria

Inclusion criteria: Age six to 12 years At least 2 opposite molars without caries Cooperation and acceptance of the patient Absence of Cl I and Cl II and ? Cl caries in the tooth Absence of oral habits such as clenching and bruxism and heavy occlusion in the teeth The presence of fully erupted teeth Molar teeth with pits and deep fissures with the possibility of caries in the future No previous dental treatment on the tooth Absence of opac-gray shadows on the bottom of the grooves

Exclusion criteria

Exclusion criteria: Taking any medication that affects the flow of saliva Presence of medical problems interfering with the study

Design outcomes

Primary

MeasureTime frame
Durability of pit and fissure sealant material. Timepoint: 6 months after the intervention. Method of measurement: Intraoral probe and mirror and observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPardiss Ebrahimnezhad

Sanandaj University of Medical Sciences

Pardis.ebrahimnezjad@gmail.com+98 13 3351 6130

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026