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Evaluating the effects of ibuprofen administration before surgery on reduction of pain after removal of wisdom teeth in women and men

Comparative effects of ibuprofen administration before surgery on reduction of pain after removal of impacted third molar between women and men

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT201204279566N1
Enrollment
60
Registered
2014-04-17
Start date
2013-08-01
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

Third molar extraction. An impacted tooth is a tooth that has failed to erupt because of obstruction by another tooth

Interventions

Administration of 400 mg ibuprofen tablet before usual third molar extraction by a surgeon.
Treatment - Drugs
Administration of 400 mg ibuprofen tablet before usual third molar extraction by a surgeon

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria 1. have impacted third molar in lower jaw (one or two side) 2. Having teeth needed partial removal of bone for extraction 3. Lack of history of GI disease and peptic ulcer 4. Lack of systemic diseases such as diabetes, chronic renal failure, chronic hepatic impairment, ... 5. Lack of hypersensitivity to aspirin or related compounds 6. Lack of use of drugs that interfere with analgesic effects of NSAIDs. Exclusion criteria: 1- Active infection immediately before or after surgery. 2- Use of other analgesics within 8 hours of surgery. 3- History of gastric ulcers or erosion. 4-history of anti coagulation therapy 5- History of asthma, nasal polyps, and allergic disorders associated with aspirin and other NSAID. 6- Uncontrolled systemic diseases 7- Female patients who were pregnant or who were not using an accepted from of birth control.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: Within 24 hrs of surgery with 2 hrs time intervals. Method of measurement: VAS.

Secondary

MeasureTime frame
Total analgesic consumption and time to first analgesic use. Timepoint: Within 24 hrs after the surgery. Method of measurement: Self report.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Masoumeh Emamghoreishi

Shiraz University of Medical Sciences- Medical School

emamm@sums.ac.ir+98 71 1230 7591

Outcome results

None listed

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