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

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

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07718607
Enrollment
56
Registered
2026-07-22
Start date
2026-07-31
Completion date
2026-10-31
Last updated
2026-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Root Canal Infection

Brief summary

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.

Interventions

PROCEDUREReciprocating rotary single-file system

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

PROCEDUREWave One Gold rotary file system

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

Sponsors

Minia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
19 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* Pregnancy or lactation * Patients with para functional habits. * Teeth with non-vital pulps and periapical lesions. * The presence of swelling or a fistulous tract. * Any periodontal pockets with a depth more than 5 mm. * Previous endodontic fillings. * Patients with a history of any systemic diseases. * Severely curved canals and calcified ones.

Design outcomes

Primary

MeasureTime frameDescription
Pain assessmentafter (6) hours, (12) hours, (24) hours, (48) and (72) hours of the procedureassessment of pain on Visual Analog Scale (VAS) scoring system

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 23, 2026