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

Clinical and Radiographic Assessment of Photobiomodulated MTA Pulpotomy in Immature First Permanent Molars with Irreversible Pulpitis: a Randomized Controlled Clinical Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06730360
Enrollment
72
Registered
2024-12-12
Start date
2024-10-10
Completion date
2026-04-05
Last updated
2024-12-17

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

Conditions

Dental Caries, Irreversible Pulpitis

Keywords

Irreversible pulpitis, Immature permanent molars, Vital pulp therapy (VPT), Mineral trioxide aggregate (MTA), Photobiomodulation (PBM)

Brief 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.

Detailed description

This randomized controlled trial evaluates the clinical and radiographic outcomes of MTA pulpotomy, with and without PBM, for immature permanent molars diagnosed with irreversible pulpitis. The study includes two parallel groups of 36 children each. Group I will undergo MTA pulpotomy alone, while Group II will receive PBM treatment alongside MTA pulpotomy. PBM employs low-level laser therapy to stimulate pulp tissue regeneration, enhance mitochondrial activity, and reduce inflammation and pain, thereby potentially improving MTA pulpotomy outcomes. Key inclusion criteria involve children with deep carious lesions and clinical signs of irreversible pulpitis but without pulpal necrosis. Follow-up will occur at 3, 6, 12, and 15 months post-treatment to evaluate success based on the absence of clinical symptoms (e.g., pain, tenderness) and radiographic indicators of healing. By comparing these two approaches, the study aims to provide insights into PBM's role as an adjunctive therapy for vital pulp preservation, particularly in pediatric dentistry.

Interventions

PROCEDUREMTA 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.

PROCEDUREMTA 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.

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
6 Years to 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.

Design outcomes

Primary

MeasureTime frameDescription
Clinical Success of Pulpotomy Treatment15 months post-treatment (assessed at 3, 6, 12, and 15 months).Evaluation of clinical signs and symptoms (absence of pain, tenderness to percussion, sinus tract, or swelling). Treatment is considered successful if these are absent at all follow-up visits.

Secondary

MeasureTime frameDescription
Radiographic Healing15 months post-treatment (assessed at 6, 12, and 15 months).Assessment of radiographic evidence of healing, including no periapical rarefaction, root resorption, or new furcal pathosis. Success is determined by achieving a PAI (Periapical Index) score of 1 or 2, or reduction in PAI score if preoperative rarefaction is present. Periapical Index (PAI) Scale: 1 to 5 Interpretation: 1: Normal periapical structures (better outcome) 5: Severe changes with evident bone destruction (worse outcome).
Root Development Progression15 months post-treatment (assessed at 6, 12, and 15 months)Radiographic evaluation of root maturity and the formation of a hard tissue bridge

Other

MeasureTime frameDescription
Postoperative Pain Intensity2 days post-treatment.Measured using the Wong-Baker Faces Pain Rating Scale to assess postoperative pain levels. Wong-Baker Facial Pain Rating Scale Scale: 0 to 10 Interpretation: 0: No pain (better outcome) 10: Worst pain imaginable (worse outcome).

Countries

Egypt

Contacts

Primary Contactpeter samir abdelshahed, assistant lecture
petersamir@mans.edu.eg+201141859508

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026