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Clinical Trials in Egypt / NCT06948526
Starting soon Not applicable

Evaluation of Moringa Oleifera Leaf Extract Versus Sodium Hypochlorite in Pulpectomy of Nonvital Primary Molars

NCT06948526 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-06-01
Last updated
2025-04-29

Condition(s) studied

Nonvital Primary Molars

Investigational drug(s) / intervention(s)

Moringa Oleifera Leaf Extract →Sodium Hypochlorite 1% →

Moringa Oleifera Leaf Extract: A plant-based extract derived from Moringa Oleifera leaves, used as an intracanal irrigant during pulpectomy procedures in primary molars. It is administered using a 3 ml syringe with a side-vented needle following canal preparation and working length determination. This intervention aims to evaluate the clinical and radiographic efficacy of a natural, biocompatible alternative to conventional chemical irrigants.

Sodium Hypochlorite 1%: A 1% concentration of Sodium Hypochlorite solution used as a standard intracanal irrigant in pediatric endodontics. It is administered using a 3 ml syringe with a side-vented needle after canal instrumentation. Known for its strong antimicrobial and tissue-dissolving properties, Sodium Hypochlorite serves as the active comparator in this study.

Study summary

This randomized clinical trial aims to compare the clinical and radiographic success of Moringa Oleifera leaf extract with Sodium Hypochlorite as intracanal irrigants in pulpectomy of nonvital primary molars in children aged 3-7 years. The study evaluates both clinical parameters (pain, swelling, mobility) and radiographic healing (periapical changes, root resorption) over 12 months.

Eligibility

Sex
ALL
Min age
3 Years
Max age
7 Years
Healthy volunteers
No
Inclusion Criteria: * Cooperative children aged between 3-7 years * Males/Females. * Primary molars necessitating pulpectomy diagnosed with deep dental caries with pulp necrosis and periapical pathosis or both. * Systemically healthy children Exclusion Criteria: * Medically compromised and uncooperative children * Tooth indicated for extraction due to root resorption more than two thirds of the root, teeth near exfoliation, deep subgingival caries hindering proper coronal seal. * Mobile teeth (Miller's Grade 2 or more) * Previous pulp therapy

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Faculty of Dentistry, Cairo University El-Manial Giza Governorate

More Cairo University trials in Egypt

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 NCT06948526 on ClinicalTrials.gov ↗ ← All trials in Egypt