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NCT Number: NCT06219824

Clinical and Radiographic Evaluation of Bioceramic Putty MTA Versus MTA in Pulpotomy of Immature Permanent Molars

The present study aims to evaluate the clinical and radiographic success of bioceramics putty MTA versus MTA in the pulpotomy of immature permanent molars

The main question it aims to answer is:

Will the biocermaics putty MTA have higher clinical and radiographic success rates than MTA in pulpotomy of immature permanent molars?

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Key information

Conditions

Age range

6 year–8 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Cairo university

Cairo, Egypt

About this study

limited clinical trials have reported the clinical and radiographic outcomes after pulpotomy with premixed putty bioceramic MTA and conventional MTA in young permanent molars.

MTA has various drawbacks, such as difficulty in handling, long setting time, discoloration of the tooth, and its form as a powder/liquid which raise the responsibility for major material waste. To conquer these issues, bioceramic materials have been developed premixed putty bioceramic MTA is a ready-to-use material for immediate placement with zero waste, saving cost and chair time. Thus, the present study aims to evaluate bioceramic putty MTA's clinical and radiographic success versus MTA in pulpotomy of immature permanent molars.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged from 6-8 years of both sexes have immature permanent molars
  • with deep carious lesions indicated for pulpotomy.
  • Restorable young permanent molars with no clinical symptoms of irreversible pulpitis.
  • Permanent molars without any clinical sign of pulp necrosis including swelling, fistula, pain on percussion, and pathologic tooth mobility.
  • Permanent molars without any adverse radiographic findings including thickening of the periodontal ligament space, radiolucency at the interradicular or periapical regions
  • permanent molars without internal and external root resorption, or calcification in pulp tissue.

Exclusion criteria

  • Medically compromised patients who have systemic disease.
  • Uncooperative patients who refuse treatment.
  • Permanent molars that were previously restored.

Treatment and study plan

premixed Bio-ceramic MTA

Drug

pulpotomy treatment will be done and the premixed bioceramic MTA will be applied in the pulp chamber

Other names: well Root MTA

Conventional MTA

Drug

pulpotomy treatment will be done and powder and liquid MTA will be mixed and applied in the pulp chamber

Other names: Pro-root MTA

Primary outcomes

  1. Primary Outcome

    Time frame: 24hrs, 1 week

    Immediate Postoperative pain [ Time Frame: one week) post operative pain by Verbal analogue scale.It is a 10 cm long horizontal line with points labeled from 0 to 10 where (0) indicates no pain, (1-3) mild pain, (4-6) moderate pain, and (7-10) severe pain.

Secondary outcomes

  1. Secondary outcome

    Time frame: 6,12 month

    The increase in root length, The root lengthening will be assessed in Mm through Digora software

Study contacts

Contact information is provided by the study sponsor or research team.

Marwa Ad Hussien, MSD

CONTACT

[email protected]

01222156972

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

Clinical and Radiographic Evaluation of Bioceramic Putty Mineral Trioxide Aggregate Versus Mineral Trioxide Aggregate in Pulpotomy of Immature Permanent Molars: A Randomized Clinical Trial

Acronym: MTA

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jan 23, 2024
Registry last updated
Jul 23, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.