Diode Laser Pulpotomy of Mature Permanent Molars With Irreversible Pulpitis

A

Alexandria University

Status

Active, not recruiting

Conditions

Irreversible Pulpitis

Treatments

Procedure: pulpotomy
Device: Diode laser - fonalaser

Study type

Interventional

Funder types

Other

Identifiers

NCT05427851
Darinemamdouh

Details and patient eligibility

About

Thirty six patients are included in this study. For each patient, a pulpotomy procedure is performed.

Full description

For each patient, a pulpotomy procedure is done. Group I (n=12) pulpotomy is performed and hemostasis is achieved by applying NaOCl, then the radicular pulp is covered with Platelet Rich Fibrin (PRF) and capped with Biodentine, Group II (n=12) pulpotomy is done as in group I and hemostasis is achieved using diode laser and remaining pulp is capped with Biodentine, Group III (n=12) pulpotomy is performed and hemostasis is achieved as in group II then radicular pulp is covered with PRF then capped with Biodentine, The teeth are then restored with Glass ionomer cement followed by composite restoration. Pain is recorded every 24 hours for 7 days after intervention. Clinical and radiographic follow-up are done at 1,3,6,9 and 12 months. Cone beam computed tomography (CBCT) is done immediate postoperative and will be used for the assessment of the outcome of the pulpotomy procedure at the end of the study period.

Enrollment

36 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Patients between 18 and 40 years of age.
  2. Deep caries in a permanent lower molar with mature roots.
  3. Clinical diagnosis of symptomatic irreversible pulpitis
  4. No signs of pulpal necrosis including sinus tract or swelling.
  5. Vital bleeding pulp tissue should be present in all canals after complete pulpotomy.
  6. The tooth is restorable.

Exclusion criteria

  1. Patients with systemic disease.
  2. Negative response to cold testing.
  3. Presence of sinus tract or swelling.
  4. No pulp exposure after caries excavation.
  5. Bleeding could not be controlled
  6. Absence of bleeding from any of the canals.
  7. Teeth with radiographic signs of internal resorption.
  8. Pulpal calcifications.
  9. Non-restorable teeth

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

36 participants in 3 patient groups

Group I: Platelet rich Fibrin (PRF) and Biodentine
Experimental group
Treatment:
Procedure: pulpotomy
Group II: Diode Laser and Biodentine
Experimental group
Treatment:
Device: Diode laser - fonalaser
Procedure: pulpotomy
Group III: Diode laser + PRF + Biodentine
Experimental group
Treatment:
Device: Diode laser - fonalaser
Procedure: pulpotomy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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