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Comparison of Anahil Plus and Ibuprofen effect for pain relief after root canal treatment in patients referred to Amol private clinic - a clinical trial study

Comparison of Anahil Plus and Ibuprofen effect for pain relief after root canal treatment in patients referred to Amol private clinic - a clinical trial study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220517054898N1
Enrollment
90
Registered
2023-09-03
Start date
2023-08-24
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

A patient with a three-channel maxilla and mandible molar tooth diagnosed with irreversible pulpitis (and the absence of periodontitis).

Interventions

Intervention 1: Intervention group:The studied patients are randomly divided into three groups of 30 people A, B and C.Intervention group A Anahil Plus capsule containing 150 mg bromelain and 300 mg t
every 8 hours up to 5 days (one dose is taken one hour before treatment and after treatment every 8 hours up to 5 days)Infraalveolar block anesthesia is performed using 1.8 ml of 2% lidocaine with 1/8

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Irreversible pulpitis in three canal molar teeth Patients with pain before endo operation in the range of moderate pain (VAS 4-7) Patients with a minimum age of 20 Systemically healthy patients

Exclusion criteria

Exclusion criteria: Patients with pain before endo operation in the range of severe pain Teeth diagnosed with necrosis and periapical periodontitis Patients with severe stress and anxiety Pregnant patients

Design outcomes

Primary

MeasureTime frame
Pain intensity reported by patients based on the VAS scale. Timepoint: Before treatment_8 hours after treatment_48 hours after treatment_5 days after treatment. Method of measurement: The method of variable measurement is VAS questionnaire, the scale of this questionnaire is classified from zero to ten. The method of using the Visual Anxiety Scale (VAS) pain questionnaire was taught to the patient. Before starting the work, the patients were asked to record the pain score before endo treatment, 8 and 48 hours and on the fifth day after endo treatment.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNarjes hoshyari

Mazandaran University of Medical Sciences

narjeshoshyari@rocketmail.com+98 11 3325 4135

Outcome results

None listed

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