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Comparative Assessment of the Effect of Ibuprofen and ketorolac on Edema Trismus and Pain after lower Third Molar Surgery

Comparative Assessment of the Effect of Ibuprofen and ketorolac on Edema Trismus and Pain after lower Third Molar Surgery

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191014045101N1
Enrollment
20
Registered
2020-01-19
Start date
2020-01-25
Completion date
Unknown
Last updated
2020-02-24

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

Conditions

Mandibular Impacted Teeth Surgery.

Interventions

Intervention 1: Intervention group: Ibuprofen Consumer: Ibuprofen 200 mg (Caspian Pharmaceutical Company)

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1) Age between 16 and 35 years 2) Any systemic disease of any body organ such as anemia, epilepsy, diabetes, hypertension, hyperthyroidism, osteoporosis or digestive disease, addicts and alcoholics who put surgery at risk Either inhibits the administration of the drug or makes it difficult to repair the surgical area 3) The presence of any localized lesions including odontogenic cysts or tumors (dependent or non-dependent on the third molar) trauma to the area or any signs of inflammation (pericoronitis) or Infection 4) No use of any drug, especially anti-inflammatory drugs 3 days before surgery 5) No history of NSAID sensitivity (ibuprofen or ketorolac) 6) Lack of any conditions that may include impaired immunity (including one year's history of chemotherapy, use of immunosuppressants)

Exclusion criteria

Exclusion criteria: 1) Patients who have only one tooth extracted and who have not been referred to the opposite tooth for surgery 2) Patients who have not taken their medication as prescribed 3) Patient non-cooperation

Design outcomes

Primary

MeasureTime frame
Edema Trismus and Pain. Timepoint: Before surgery and 2 and 7 days after surgery. Method of measurement: In the post-treatment period, pain ratings will be assessed by reporting pain scores on an 11-point visual Analogue scale by patients at 6, 12, and 24 hours after surgery. Edema assessment is performed by measuring intervals such as the interval between the tip of the chin to the lower edge of the ear fins and the mandibular tooth line before and 2 and 7 days after surgery. Evaluation of mouth opening will be done by measuring the maximal distance between the incisal edges of the anterior teeth before and 2 and7 days after surgery.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDR.MOSTAFA GAVAHI

Yazd University of Medical Sciences

mgdds@ssu.ac.ir+98 35 3827 9615

Outcome results

None listed

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