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Clinical Trials in Egypt / NCT06730360
Recruiting Not applicable

Clinical and Radiographic Assessment of Photobiomodulated MTA Pulpotomy in Immature First Permanent Molars with Irreversible Pulpitis

NCT06730360 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2024-10-10
Last updated
2024-12-17

Condition(s) studied

Dental CariesIrreversible Pulpitis

Investigational drug(s) / intervention(s)

MTA Pulpotomy without photobiomodulationMTA Pulpotomy with Photobiomodulation (LLLT)

MTA Pulpotomy without photobiomodulation: This intervention involves the application of Mineral Trioxide Aggregate (MTA) to the pulp chamber after the removal of the coronal pulp tissue in first permanent molars with irreversible pulpitis. The procedure is performed without the use of photobiomodulation (low-level laser therapy). The MTA is placed as a seal to preserve the vitality of the remaining radicular pulp.

MTA Pulpotomy with Photobiomodulation (LLLT): This intervention combines MTA pulpotomy with photobiomodulation (low-level laser therapy). After performing the MTA pulpotomy, low-level laser therapy is applied to the pulp stumps to reduce inflammation, promote healing, and modulate pain. The laser therapy uses specific wavelengths of light to stimulate cellular activity and enhance the regeneration of pulp tissue.

Study summary

This study evaluates the effectiveness of photobiomodulation (PBM) in conjunction with mineral trioxide aggregate (MTA) pulpotomy for treating irreversible pulpitis in immature first permanent molars. PBM, also known as low-level laser therapy (LLLT), is used to enhance healing, reduce inflammation, and manage pain in young teeth. The randomized clinical trial involves 72 children aged 6-9 years, divided into two groups: one receiving MTA pulpotomy alone and the other receiving MTA pulpotomy with PBM. Clinical and radiographic outcomes will be assessed at intervals over 15 months. This research aims to determine the combined therapy's efficacy in improving pulp healing and reducing post-operative discomfort compared to MTA alone.

Eligibility

Sex
ALL
Min age
6 Years
Max age
9 Years
Healthy volunteers
No
Inclusion Criteria: * Children aged 6 to 9 years. * Non-contributory medical history (healthy otherwise). * Presence of carious first permanent molars with the following characteristics: * Deep caries extending to ≥2/3 of dentin. * Positive response to cold testing. * Clinical diagnosis of irreversible pulpitis (moderate or severe), with or without periapical periodontitis. * Restorable tooth. * Probing pocket depth and mobility within normal limits. * No signs of pulpal necrosis, including sinus tract or swelling. Exclusion Criteria: * Insufficient bleeding after pulp exposure (indicating necrotic or partially necrotic pulp). * Presence of systemic or medical conditions that may contraindicate participation. * Teeth with unrestorable structure. * Teeth showing signs of pulpal necrosis, such as the presence of a sinus tract or swelling.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Faculty of Dentistry Al Mansurah Dakahlia Governorate Recruiting

More Mansoura 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 NCT06730360 on ClinicalTrials.gov ↗ ← All trials in Egypt