Status:

COMPLETED

Sodium Hypoclorite as an Antibacterial Agent Prior to Pulpotomies

Lead Sponsor:

Izmir Katip Celebi University

Conditions:

Pulpotomy

Primary Teeth

Eligibility:

All Genders

6-10 years

Phase:

NA

Brief Summary

Aim: The aim of this study was to report the 24-Month radiographical and histological outcome on these previously reported calcium hydroxide (CH) and mineral trioxide aggregate (MTA) pulpotomies using...

Detailed Description

The procedure and possible discomforts, risks, and benefits had been fully explained to the parents of the children, and informed consent forms were signed. A total of 64 children (37 boys and 27 gir...

Eligibility Criteria

Inclusion

  • Each child had at least two previously untreated lower 2nd primary mandibular molars with nearly equal carious involvement that required pulpotomies but showed positive response to vitality tests (electrical pulp test and cold stimulation)
  • The children were healthy and cooperative
  • Moderate response to chemical and thermal stimuli.
  • Teeth would be restorable with stainless steel crowns.

Exclusion

  • Signs of irreversible pulpitis (such as spontaneous pain, prolonged pain response),
  • Presence of percussion or palpation,
  • Pathological mobility,
  • Infectious symptoms such as fistula or abscess,
  • Discoloration in the clinical examination,
  • Presence of radiolucency in the furcation or periodical regions thickening of the periodontal spaces
  • Internal or external root resorption.

Key Trial Info

Start Date :

September 1 2012

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

March 1 2017

Estimated Enrollment :

64 Patients enrolled

Trial Details

Trial ID

NCT04270318

Start Date

September 1 2012

End Date

March 1 2017

Last Update

February 17 2020

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