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Clinical Trials in Egypt / NCT07765745
Recruiting Not applicable

Effect of Thymoquinone 0.2% Gel on Bone Density, Bone Width, and Socket Preservation After Tooth Extraction

NCT07765745 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2026-02-01
Last updated
2026-08-14

Condition(s) studied

Radiographic EvaluationBone DensityBone WidthSocket PreservationTooth ExtractionThymoquinone

Investigational drug(s) / intervention(s)

Gel foamThymoquinone gel + gel foamNano-formulated 0.2% thymoquinone gel + gel foam

Gel foam: Patients will receive gel foam only.

Thymoquinone gel + gel foam: Patients will receive 0.2% thymoquinone gel + gel foam.

Nano-formulated 0.2% thymoquinone gel + gel foam: Patients will receive nano-formulated 0.2% thymoquinone gel + gel foam.

Study summary

This study aims to evaluate the clinical and radiographic effects of 0.2% Thymoquinone gel on bone density, bone width, and socket preservation after tooth extraction.

Eligibility

Sex
ALL
Min age
18 Years
Max age
50 Years
Healthy volunteers
No
Inclusion Criteria: * Age: 18-50 years. * Both sexes. * Patients requiring extraction of upper posterior teeth will be recruited. Exclusion Criteria: * Healthy subjects with intact sockets after extraction. * Normal mouth opening and good oral hygiene. * No systemic conditions affecting bone healing.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kafrelsheikh University Kafr ash Shaykh Kafrelsheikh Recruiting

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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 NCT07765745 on ClinicalTrials.gov ↗ ← All trials in Egypt