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Comparison of the analgesic effect of odontopaste and a medicament with similar formulation between root canal therapy appointments

Comparison of the analgesic effect of odontopaste and a medicament with similar formulation in pain control after emergency treatment in the patients with lower posterior tooth pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201110196443N2
Enrollment
96
Registered
2012-11-17
Start date
2012-01-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Condition 1: Toothache. Condition 2: Acute apical periodontitis. Toothache NOS Acute apical periodontitis NOS

Interventions

Intervention 1: Intracanal medicament insertion. Intervention 2: Intracanal medicament similar to odontopaste containing clindamycin and triamcinolone insertion. Intervention 3: Placebo containing eth
Treatment - Drugs
Intracanal medicament insertion
Intracanal medicament similar to odontopaste containing clindamycin and triamcinolone insertion
Placebo containing ethyle cellolose

Sponsors

Research assistance Of Ahwaz University Of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: The spontaneous pain or sensitivity to percussion before treatment;The tooth should be first or second molar;the patient should be without any systemic problem, female should not be pregnant or in lactating stage;The patients do not have any history of oral diseases or hypersensitivity to antibiotics or corticosteroid;The tooth should have a normal apex;The roots were without resorption and pathological problems such as periapical lesions;The patients were not be used NSAIDs medicine 1 hour before treatment. Exclusion criteria: If the patient has severe pain,is exclude from seven days evaluation and prescribe analgesic;The patient has not be satisfied to continue in study;If the patient did not confer seven days later;The procedure accidents;If the pain rate did not record at 24 hours after the first appointment;If the patient used analgesic.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Toothache. Timepoint: Before first appointment-24 hours after intracanal medicament insertion-7 days after intracanal medicament insertion. Method of measurement: Use of VAS diagram.;Acute apical periodontitis. Timepoint: Before first appointment-24 hours after intracanal medicament insertion-7 days after intracanal medicament insertion. Method of measurement: Use of VAS diagram.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPejman Pourakbar Jahandideh

Endodontic Department Of Dental Faculty

pejman.jahandideh@gmail.compejman_tornado@yahoo.com+98 61 1336 1984

Outcome results

None listed

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