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The effect of AH26 and Resil sealers on pain after endodontic treatment

The effect of AH26 and Resil resin sealers on postoperative pain after endodontic treatment in patient with irreversible pulpitis: A randomized controlled clinical trial study

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150720023253N5
Enrollment
100
Registered
2022-05-10
Start date
2022-05-10
Completion date
Unknown
Last updated
2022-05-30

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

Conditions

Irreversible pulpitis. Pulpitis

Interventions

Intervention 1: Intervention group: After canal preparation and selecting the gutta-percha cone, the AH26 resin sealer is placed in the canals for obturation. Intervention 2: Intervention group: After

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients aged 18 to 60 years Patients who do not have systemic problems and immunosuppression and are not treated with medication. Patients who are not allergic to the medicines used during endodontic treatment and local anesthetics. Patients with a long-term positive pulp response to the cold test and EPT (moderate to severe responses (vas = 40-100)) or long and delayed responses. Patients diagnosed with irreversible pulpitis in the first or second mandibular molars. Patients with healthy periapical tissue (confirmed by radiography and clinic)

Exclusion criteria

Exclusion criteria: Symptomatic teeth that need emergency endodontic treatment. Teeth that have been treated in two sessions. Patients who have been taking analgesics or antibiotics for the past seven days. Patients with periodontal disease (probe depths greater than 4 mm). Teeth with open apex, apical resorption, or canal calcification. Patients who have multiple teeth in need of endodontic treatment. Teeth that have been treated with crown. Patients taking antibiotics after treatment for any reason. Patients with allergies to nonsteroidal anti-inflammatory drugs Patients who are pregnant or breastfeeding. Overfilling treatments (gutta-percha or sealer extrusion beyond radiographic apex). Under filing treatments (more than 2 mm shorter than radiographic apex). Teeth with severe crown destruction need core build-up crowns.

Design outcomes

Primary

MeasureTime frame
Number of pain after root canal treatment. Timepoint: 6,12,24,48 hours after treatment and 3,4,5,6 and 7 days after treatment. Method of measurement: visual analog scale.;Dosage of analgesics consumption. Timepoint: 6,12,24,48 hours after treatment and 3,4,5,6 and 7 days after treatment. Method of measurement: Number of medicaments taken.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Nazanin Zargar

Shahid Beheshti University of Medical Sciences

nzargar48@yahoo.com+98 21 2217 5350

Outcome results

None listed

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