Post Operative Pain of Partial Pulpotomy Using a Bioceramic Material in Patients With Symptomatic Irreversible Pulpitis

Evaluation of Postoperative Pain After Partial Pulpotomy Versus Full Root Canal Treatment in Managing Young Permanent Molars With Symptomatic Irreversible Pulpitis: a Randomized Controlled Trial

Status

Completed

Phases

Early Phase 1

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT05956613

Enrollment

Registered

2023-07-21

Start date

2023-08-01

Completion date

2023-10-22

Last updated

2024-05-14

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

Conditions

Endodontic Disease

Keywords

bioceramic material, pulpitis, partial pulpotomy

Brief summary

The goal of this clinical trial is to assess post-operative pain of partial pulpotomy using a newly introduced Bioceramic material in young patients with symptomatic irreversible pulpitis at 24, 48, 72 hours postoperatively using visual analogue scale (VAS). The main question\[s\] it aims to answer are: • In patients with symptomatic irreversible pulpitis does the use of bioceramic material in partial pulpotomy decrease amount of post operative pain in comparison to conventional root canal treatment? Participants will record the intensity of pain at 24,48, 72 hours postoperatively.

Interventions

PROCEDUREPartial pulpotomy

Use of newly introduced bioceramic putty in partial pulpotomy

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender

ALL

Age

9 Years to 14 Years

Healthy volunteers

Yes

Inclusion criteria

1. Inclusion criteria : 1. Subject's age between 9-14 years. 2. Both male and female subjects. 3. Medically free and healthy subjects. 4. Mandibular molar teeth. 5. Teeth with symptomatic irreversible pulpitis. 6. Teeth with mature closed apices. 2.

Exclusion criteria

1. Teeth with acute dentoalveolar abscess. 2. Subjects having more than one tooth that require root canal treatment. 3. Subjects that have taken analgesic, anti-inflammatory or antibiotic drugs during the 10 days prior to the start of treatment. 4. Subjects with systemic diseases who have endocrine diseases, Infectious diseases or Psychological disturbance. 5. Teeth with periodontal disease or pulp calcification. 6. Subjects taking chronic pain medications.

Design outcomes

Primary

Measure	Time frame	Description
Post operative pain	after 24 hours	Measure intensity of post operative pain using visual analogue scale (VAS)

Countries

Egypt

Outcome results

None listed

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