Comparing MTA Pulpotomy to Root Canal Treatment in Management of Permanent Molars With Irreversible Pulpitis in Children

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age10-14
SponsorAin Shams University

About this trial

Dental caries, highly prevalent amongst children, can cause pulpitis. Coronal pulpotomy provides an easier, cost-effective, conservative and biologically-driven treatment option compared to endodontic treatment in mature permanent teeth with irreversible pulpitis.

The aim of the current study is to evaluate postoperative pain, clinical and radiographic outcomes of MTA pulpotomy compared to root canal treatment in children's first permanent molars suffering from irreversible pulpitis.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Healthy male and female children, aged 10 to 14 years

Signs and symptoms of irreversible pulpitis in carious first permanent molar.

Disqualifiers

Molars with immature roots

Non-restorable molars, with abnormal mobility or increased probing pocket depth (normal range = 1-3 mm)

Any indication of pulpal necrosis, such as sinus tract or swelling or no bleeding from orifices after access opening.

Any signs of periapical or furcal rarefaction.

Trial design

Design model

Parallel

Treatments tested in this trial

  • MTA Pulpotomy

    Procedure/Surgery

    Complete coronal MTA pulpotomy.

  • Root Canal Treatment

    Procedure/Surgery

    Conventional root canal treatment.

Treatment groups

62 Participants
are divided into 2 treatment groups
Group A: MTA PulpotomyExperimental treatment 1 intervention
Group B: Root Canal TreatmentActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Pain Relief

A 10 cm visual analogue scale will be used to record pain

Time frame
preoperatively, immediately postoperatively and every 24 hours for 7 days after the first appointment.

Secondary outcomes

1

Clinical Evaluation

* Absence of pain or discomfort * Tooth is functional, with no tenderness to palpation or percussion * Normal mobility and probing depth * Soft tissues surrounding the tooth are normal, with no swelling or inflammation

Time frame
3, 6, 12 and 18 months postoperatively
2

Radiographic Evaluation

* No evident radiographic periapical or furcal pathosis * No evident root resorption * Normal lamina dura

Time frame
6, 12 and 18 months postoperatively

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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