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Postoperative Pain After Pulpotomy in Children Using Calcium Silicate Cements With and Without Laser Therapy

Evaluation of Postoperative Pain After Pulpotomy Using Calcium Silicate Cements in Permanent Molars with and without Laser Biomodulation: A Randomized Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111415
Enrollment
Unknown
Registered
2025-10-30
Start date
2025-10-30
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

Symptomatic Irreversible Pulpitis

Interventions

Control Group:Intervention Type: Vital pulp therapy (Pulpotomy) Intervention Name: EndoCem Pulpotomy Dose: A single application of 2–3 mm thickness of EndoCem premixed putty (MTA-based calcium silic
Trial Group:Intervention Type: Vital pulp therapy (Pulpotomy with adjunctive laser biomodulation) Intervention Name: EndoCem Pulpotomy with Adjunctive Er,Cr:YSGG Laser Biomodulation Dose: A single a

Sponsors

Fujairah University, United Arab Emirates
Lead Sponsor

Eligibility

Sex/Gender
All
Age
9 Years to 14 Years

Inclusion criteria

Inclusion criteria: 1. Patient’s age ranges from 9-14 years old; 2. Two Rooted Mandibular Molar teeth diagnosed with symptomaticirreversible pulpitis; 3. The teeth are restorable; 4. Informed consent granted; 5. Teeth are periodontally free, with no mobility and negative to percussion and palpation test.

Exclusion criteria

Exclusion criteria: 1. Teeth with immature root tips. 2. Teeth that are not restorable (severely damaged or decayed). 3. Bleeding from the tooth's nerve that cannot be controlled within 10 minutes during the procedure. 4. Patients with significant medical conditions that could complicate dental treatment. 5. Teeth with a dead (necrotic) nerve. 6. Inability or unwillingness to provide informed consent. 7. Individuals from vulnerable groups (as defined by the ethics committee).

Design outcomes

Primary

MeasureTime frame
Postoperative Pain Intensity as assessed by Visual Analogue Scale (VAS);

Secondary

MeasureTime frame
Radiographic Success Rate;

Countries

United Arab emirates

Contacts

Public ContactProf. Mohamed Medhat Kataia

Fujairah University, United Arab Emirates

m.kataia@fu.ac.ae+971 9 202 3518

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026