🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Egypt / NCT07171229
Starting soon Not applicable

Evaluation of Cytokines Level as an Indicator of Pulp Inflammation and Its Relation to the Success Rates of Pulpotomy in Primary Molars Affected With Proximal Versus Occlusal Decay

NCT07171229 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-09-01
Last updated
2025-09-12

Condition(s) studied

Pulpitis - ReversibleOcclusal CariesProximal Caries

Investigational drug(s) / intervention(s)

PulpotomyMeasuring Cytokines level

Pulpotomy: * Local anesthesia will be administered, and the tooth will be isolated with a rubber dam. * To minimize further bacterial contamination, carious tissues will be removed progressively, starting from the cavity periphery and then over the pulp chamber roof. * Before managing the pulpal hemorrhage, a sterile cotton pellet will be placed over the pulp tissue for 30-45 s. * A fresh sterile bur will be used to remove all coronal pulp tissue down to the root canal orifices, with copious water irrigation * MTA will be used as medicament of choice for pulpotomy. * The pulpotomy-treated tooth will be prepared to receive a full-coverage stainless steel crown (SSC) after the procedure.

Measuring Cytokines level: measuring cytokines level as an indicator for pulp inflammation

Study summary

pulpotomy will be done I primary molars with occlusal or proximal decay and level of cytokines will be measured as an indicator for pulp inflammation levels

Eligibility

Sex
ALL
Min age
4 Years
Max age
9 Years
Healthy volunteers
No
Inclusion Criteria: * Children with provoked pain. * Caries in proximal surface to the dentine full thickness. * Caries in occlusal surface to the dentine full thickness. * Radicular pulp health is verified by achieving hemostasis within eight minutes of compression using a cotton pellet with 5% sodium hypochlorite. Exclusion Criteria: * Unrestorable primary molars. * Primary molars with spontaneous pain. * Medically compromised patients who have systemic disease. * Uncooperative children who refuse treatment. * Children whose parents are unwilling to place stainless steel crowns. * Children whose parents or caregivers refuse to participate in the study or are unable to attend follow-up visits.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Cairo Univeristy Cairo Egypt

More Cairo University trials in Egypt

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 NCT07171229 on ClinicalTrials.gov ↗ ← All trials in Egypt