Growth factor versus mineral trioxide aggregate for treating mature permanent molars with irreversible pulpitis in children

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Children with a restorable mature permanent molar and a closed apex diagnosed with symptomatic irreversible pulpitis will receive either a concerned growth factor application or mineral trioxide aggregate applied to the affected tooth at Minia University Faculty of Dentistry. The interventions are intended to manage pulpal inflammation and preserve tooth vitality, though specific operative details were not provided. Eligible participants exclude medically compromised children, non-restorable teeth, and necrotic teeth. The study will monitor clinical outcomes such as symptom relief and tooth survival over follow-up, but exact endpoints and timing were not listed.

Why it matters

Who can join: the full rules

Inclusion Criteria: Permanent Molar with closed Apex and diagnosed with irreversible pulpitis

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Exclusion Criteria:

* medically compromised children.

  * non restorable tooth
  * Necrotic tooth

Where it's running

• Minya University Faculty of Dentistry
  Minya, Egypt Recruiting

Study contacts

• Study coordinator: Mahmoud Mostafa Abdelhakim, Master degree
• Email: mahmoudmostafa100001@gmail.com
• Phone: 201004445513

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.