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Impact of Preemptive Intravenous Ibuprofen on Intraoperative Analgesia in Third Molar Teeth

E

Erzincan University

Status

Unknown

Conditions

Intraoperative Analgesia
Preemptive Intravenous Ibuprofen

Treatments

Drug: intrafen 800 mg
Other: plasebos
Drug: arveles

Study type

Interventional

Funder types

Other

Identifiers

NCT03170726
ERZINCAN UNIVERSITY 9

Details and patient eligibility

About

This study was planned to evaluate the analgesic efficacy of preemptive intravenous (iv) ibuprofen on pain occurring during and after the mandibular third molar surgeon

Enrollment

60 estimated patients

Sex

All

Ages

20 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who are to be elected third molar tooth extraction
  • Patients between the ages of 20-35
  • Patients who are symptomatic
  • Third molar tooth angular or horizontal settled patients

Exclusion criteria

  • Patients who refuse to participate in the study
  • Patients under 20 years old, over 35 years old
  • Patients who are allergic to known non-steroidal anti-inflammatory drugs
  • Pregnant patients
  • Patients with severe liver failure,
  • patients with severe renal insufficiency

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 3 patient groups, including a placebo group

arveles
Active Comparator group
Description:
Ibuprofen 800 mg in normal saline 150 cc and dexketoprofen (50 mg) before operation will be given in 30 minutes
Treatment:
Drug: arveles
Other: plasebos
Drug: intrafen 800 mg
intrafen
Active Comparator group
Description:
intrafen 800 mg in normal saline 150 cc before operation will be given in 30 minutes
Treatment:
Drug: arveles
Other: plasebos
Drug: intrafen 800 mg
plasebos
Placebo Comparator group
Description:
150 cc normal saline will be given in 30 minutes during preoperative period
Treatment:
Drug: arveles
Other: plasebos
Drug: intrafen 800 mg

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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