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Effect of commonly used analgesics on response of teeth with symptomatic, irreversible pulpitis to pulp vitality tests

?Study of the effect of commonly used analgesics on response of teeth with symptomatic, irreversible pulpitis to pulp vitality tests

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200322046836N1
Enrollment
54
Registered
2020-05-04
Start date
2019-05-22
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Symptomatic irreversible pulpitis. Irreversible pulpitis

Interventions

Intervention 1: Intervention group: a single dosage of 400 mg Gelofen (Dana,Tehran,Iran) was prescribed and then dental vitality tests were carried out at 20, 40 and 60 minute later. Intervention 2:

Sponsors

Tehran university of medical science, International campus
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: age between 18 to 65 years, systemic health, emergency admission due to symptomatic irreversible pulpitis with moderate to severe pain and prolonged pain response to cold test, and no history of analgesic intake or use of nervous system depressants during the past 6 h.

Exclusion criteria

Exclusion criteria: contraindication for taking acetaminophen and/or Gelofen, patients whose tooth did not response to cold test, and those who had dental pain originated from periapical tissues.

Design outcomes

Primary

MeasureTime frame
The pulp response to cold test in teeth with symptomatic irreversible pulpitis and sound teeth in Visual Analogue Scale. Timepoint: at the onset of study and at 20, 40 and 60 minutes after medication intake. Method of measurement: The values are based on Visual Analogue Scale and in millimeters.;The pulp response of teeth with symptomatic irreversible pulpitis and sound teeth to EPT. Timepoint: at the onset of study and at 20, 40 and 60 minutes after medication intake. Method of measurement: The degree displayed by the electric pulp tester when the patients felt pain, burning sensation or heat.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Dibaji

Tehran University of Medical Sciences

f-dibaji@tums.ac.ir0982155851149

Outcome results

None listed

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