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Comparison of acetaminophen and ibuprofen before orthodontic treatment in reducing pain

Comparison of acetaminophen and ibuprofen before orthodontic treatment in reducing pain-clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014022516746N1
Enrollment
54
Registered
2014-07-20
Start date
2014-09-23
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

Orthodontic Pain. Other specified medical care

Interventions

Intervention 1: Acetaminophen, 650 miligram oral tablet, single dose half hour before of separator placement. Intervention 2: Ibuprofen, oral tablet 400 miligram, single dose half hour before separato
Treatment - Drugs
Acetaminophen, 650 miligram oral tablet, single dose half hour before of separator placement
Ibuprofen, oral tablet 400 miligram, single dose half hour before separator placement
Placebo, oral capsul 500 miligram of starch, single dose half hour before separator placement

Sponsors

Vice Chancellor for Research and Technology of Ahvaz Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 25 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:1) no specific systemic disease; 2) currently not using analgesics; 3) no periodontal and endodontics problems. Exclusion criterion: the lack of any case inclusion criteria.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The measure of pain. Timepoint: Before of interference, Immediate after interference, 2-3 hours after interference,atthe bed time, at the morning of 2,3,4 and 5 days after interference. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Measure of pain at chewing, dental contact and at rest whit no contact. Timepoint: Before of interference, Immediate after interference, 2-3 hours after interference,atthe bed time, at the morning of 2,3,4 and 5 days after interference. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParisa Kazemi

Vice Chancellor for Research and Technology of Ahvaz Jundishapur University of Medical Sciences

parisa_kazemi69@yahoo.com+98 84 2572 2339

Outcome results

None listed

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