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Recruiting NCT07340606

NCT07340606 The Role of the Pre-operative Condition and Artificial Intelligence-Assisted Diagnosis in Predicting the Success of Full Pulpotomy in Symptomatic Permanent Mature Molars

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Clinical Trial Summary
NCT ID NCT07340606
Status Recruiting
Phase
Sponsor Misr International University
Condition Pulpitis - Irreversible
Study Type INTERVENTIONAL
Enrollment 58 participants
Start Date 2026-01-17
Primary Completion 2026-08-01

Eligibility & Interventions

Sex All sexes
Min Age 20 Years
Max Age 45 Years
Study Type INTERVENTIONAL
Interventions
Conventional root canal treatmentFull pulpotomy

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 58 participants in total. It began in 2026-01-17 with a primary completion date of 2026-08-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study aims to evaluate the effect of prognostic factors, such as the severity of pulpal inflammation, carious pulp exposure, and the presence of apical periodontitis, on the success of full pulpotomy in mature permanent molars with irreversible pulpitis. It also aims to investigate the role of artificial intelligence-assisted diagnosis in predicting the prognosis of full pulpotomy.

Eligibility Criteria

Inclusion Criteria: * Mature permanent molars with irreversible pulpitis. * Presence of bleeding from all canals. * The tooth is not periodontally compromised. Exclusion Criteria: * Non-vital teeth. * Uncontrolled bleeding from any of the canals after ten minutes of application of hemostatic agent. * Molars with immature roots.

Contact & Investigator

Central Contact

Mayand A Amer, B.D.S.

✉ mayand.amer@miuegypt.edu.eg

📞 01062509703

Principal Investigator

Ahmed M Ghobashy, Prof. Dr.

STUDY DIRECTOR

Misr International University

Frequently Asked Questions

Who can join the NCT07340606 clinical trial?

This trial is open to participants of all sexes, aged 20 Years or older, up to 45 Years, studying Pulpitis - Irreversible. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07340606 currently recruiting?

Yes, NCT07340606 is actively recruiting participants. Contact the research team at mayand.amer@miuegypt.edu.eg for enrollment information.

Where is the NCT07340606 trial being conducted?

This trial is being conducted at Cairo, Egypt, Cairo, Egypt.

Who is sponsoring the NCT07340606 clinical trial?

NCT07340606 is sponsored by Misr International University. The principal investigator is Ahmed M Ghobashy, Prof. Dr. at Misr International University. The trial plans to enroll 58 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology