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Recruiting Phase 2 NCT06293521

NCT06293521 Clinical and Radiographic Success Rate of Pulpotomy Versus Pulpectomy for Management of Primary Teeth With Deep Caries

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Clinical Trial Summary
NCT ID NCT06293521
Status Recruiting
Phase Phase 2
Sponsor Cairo University
Condition Deep Caries
Study Type INTERVENTIONAL
Enrollment 40 participants
Start Date 2026-01-01
Primary Completion 2026-01-31

Eligibility & Interventions

Sex All sexes
Min Age 4 Years
Max Age 6 Years
Study Type INTERVENTIONAL
Interventions
PulpotomyPartial Pulpectomy

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.

In Phase 2, researchers evaluate early signs of effectiveness. You may be randomized to receive the active treatment or a comparator. Monitoring continues closely.

This trial targets 40 participants in total. It began in 2026-01-01 with a primary completion date of 2026-01-31.

⚠ 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 trial aims to compare treatment outcomes between Pulpotomy and Pulpectomy in treating vital primary teeth diagnosed with deep caries with symptoms of irreversible pulpits

Eligibility Criteria

Inclusion Criteria: 1. Aged 4 to 6 years , in good general health 2. The parents provided written informed consent. 3. Clinical characteristics, defined as spontaneous pain and the presence of a deep carious lesion with pulp exposure and bleeding that did not halt within five minutes following removal of the coronal pulp tissue. 4. Restorable teeth. Exclusion Criteria: 1. Physical or mental disability. 2. Unable to attend follow-up visits. 3. Previously accessed teeth. 4. Swelling, tenderness to percussion or palpation, or pathological mobility. 5. Pre-operative radiographic pathology such as resorption (internal or external), per-radicular or furcation radiolucency.

Contact & Investigator

Central Contact

Nada Mostafa, B.D.S

✉ Nadamostafa@dentistry.cu.edu.eg

📞 01117311533

Frequently Asked Questions

Who can join the NCT06293521 clinical trial?

This trial is open to participants of all sexes, aged 4 Years or older, up to 6 Years, studying Deep Caries. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT06293521 trial and what does that mean for participants?

Phase 2 trials evaluate whether the treatment shows signs of effectiveness while continuing to monitor safety. More participants are enrolled than in Phase 1 to help refine the treatment protocol.

Is NCT06293521 currently recruiting?

Yes, NCT06293521 is actively recruiting participants. Contact the research team at Nadamostafa@dentistry.cu.edu.eg for enrollment information.

Where is the NCT06293521 trial being conducted?

This trial is being conducted at Cairo, Egypt.

Who is sponsoring the NCT06293521 clinical trial?

NCT06293521 is sponsored by Cairo University. The trial plans to enroll 40 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: July 2026  ·  Data Methodology