Health TrialsbyHealthPanel

Comparison of the Effects of Bio Ceramic and Epoxy Resin-based Sealers on Postoperative Pain After Root Canal Treatment

ConditionAsymptomatic Apical Periodontitis
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorPrimary Health Care Corporation, Qatar

About this trial

This study aims to compare the effect of bio ceramic sealer and resin-based sealer on the intensity and occurrence of post operative pain in single rooted teeth with asymptomatic apical periodontitis.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Permanent single rooted tooth 1-1 configuration and complete root development.

Requiring root canal treatment.

Diagnosed with Asymptomatic apical periodontitis, teeth asymptomatic, periapical index will exhibit an apical radiolucency.

Willing to Participate.

Disqualifiers

Medically compromised patients.

Inability to reach working length, complication during treatment.

Retreatment teeth, multi rooted teeth.

Periodontological compromised teeth.

Trial design

Design model

Parallel

Treatments tested in this trial

  • AH plus sealer

    Combination product

    Root canal sealer will be placed inside the root canals during obturation procedure to seal dentine wall and reinforce the remaining tooth tissue.It will be selected randomly to the study samples.

  • Bioceramic sealer

    Combination product

    Root canal sealer will be placed inside the root canals during obturation procedure to seal dentine wall and reinforce the remaining tooth tissue.It will be selected randomly to the study samples.

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Control GroupActive comparator 1 intervention
Group B: InterventionActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

post operative pain questionnaire

The participants of the study groups will be given a questionnaire to record whether they experienced pain following the root canal treatment after applying each type of the study sealers or no, during the Time frame.

Time frame
assessed at 24 hours, 48 hours, and 7 days post-treatment.

Secondary outcomes

1

Intensity of postoperative pain

The patient will be asked to measure Intensity of their postoperative pain using a Visual Analog Scale. It consist of a straight line, usually 10 centimeters in length, with end point defining the extremes of pain. One end of the line represents no pain(usually marked as 0), while the other end represents' worst imaginable pain' (usually marked as 10) participant mark a point on the line that corresponds to their perceived pain intensity. The distance from the 'no pain' end to the mark is then measured and used to quantify the pain level during Time frame.

Time frame
assessed at 24 hours, 48 hours, and 7 days post-treatment.
2

Analgesic

Analgesic intake recorded, The participants of the study will be asked to record any analgesic taken and the number of the tables during the Time frame.

Time frame
assessed at 24 hours, 48 hours, and 7 days post-treatment.

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Primary Health Care Corporation, Qatar

Lead sponsor

Source ClinicalTrials.gov
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