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Investigating the effect of using ibuprofen and netonal drugs before root canal treatment on the pain after treatment in teeth with irreversible pulpitis

Investigating the effect of using ibuprofen and netonal drugs before root canal treatment on the pain after treatment in teeth with irreversible pulpitis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230313057710N2
Enrollment
60
Registered
2023-07-02
Start date
2019-07-03
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Pulpits. Diseases of oral cavity, salivary glands and jaws

Interventions

Intervention 1: Intervention group1: Iboprofen tablet: Before the intervention, patients completed the demographic questionnaire, visual analog pain scale, and Wong-Baker shape scale. Intervention gr

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients with irreversible pulpitis of mandibular first or second molar teeth who have been referred for treatment, The spontaneous tooth pain, according to the Visual Analogue Scale or Wong-Baker figure scale, is at least 30 mm, The radiographic appearance of the teeth in these patients is normal, Do not have lesion or a sinus tract (chronic periapical abscess), Give a long response to the electrical pulp test (EPT) and the cold test with a cotton roll cooled by endo-ice.

Exclusion criteria

Exclusion criteria: Patients who have used any sedative in the last 12 hours, Patients who have used long-term drugs that interact with NSAIDs, Patients who are allergic to NSAIDs or lidocaine or have systemic problems, Pregnant mothers, Teeth with lesions Periapical and chronic periapical abscess, Patients with aggressive periodontal disease, Patients with unrepairable or previously repaired cavities, Patients who have pain in more than one tooth.

Design outcomes

Primary

MeasureTime frame
Pulpits Pain. Timepoint: Before treatment, immediately after treatment and 8, 12 and 24 hours after treatment. Method of measurement: Using Visual analogue scale ? Wong-Baker ?Figure scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Khosravani

Esfahan University of Medical Sciences

khosravanii.zahra73sums@gmail.com+98 31 3668 0048

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026