Postoperative Pain After Using a Minimally Invasive Reciprocating Single-file System in Mandibular Molars With Symptomatic Irreversible Pulpitis

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age19-45
SponsorMinia University

About this trial

The aim of the present study is to assess the incidence and severity of postoperative pain after root canal preparation of mandibular molars with symptomatic irreversible pulpitis using a minimally invasive reciprocating single-file system in comparison to Wave One Gold.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult patients who have vital mandibular molar teeth with irreversible pulpitis without apical periodontitis.

Medically free patients.

Disqualifiers

Pregnancy or lactation

Patients with para functional habits.

Teeth with non-vital pulps and periapical lesions.

The presence of swelling or a fistulous tract.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Reciprocating rotary single-file system

    Procedure/Surgery

    One glider will be used then (25/6) will be used to prepare narrow and curved canals as mesials in lower molars, and the large file (45/4) will be used for large canals. Three in-and-out motions were applied with motions until attaining full working length

  • Wave One Gold rotary file system

    Procedure/Surgery

    Wave One Gold glider will be used then primary (25\\7) to prepare narrow and curved canals as mesials in lower molars, and the file (45/5) will be used for large canals. Three in-and-out motions will be applied with motions until attaining full working length

Treatment groups

56 Participants
are divided into 2 treatment groups
Group A: Reciprocating rotary single-file systemActive comparator 1 intervention
Group B: Wave One Gold rotary file systemActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Pain assessment

assessment of pain on Visual Analog Scale (VAS) scoring system

Time frame
after (6) hours, (12) hours, (24) hours, (48) and (72) hours of the procedure

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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