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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03170726
Other study ID # ERZINCAN UNIVERSITY 9
Secondary ID
Status Active, not recruiting
Phase N/A
First received May 20, 2017
Last updated May 26, 2017
Start date May 15, 2017
Est. completion date November 15, 2017

Study information

Verified date May 2017
Source Erzincan University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 60
Est. completion date November 15, 2017
Est. primary completion date October 30, 2017
Accepts healthy volunteers No
Gender All
Age group 20 Years to 35 Years
Eligibility 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

Study Design


Intervention

Drug:
arveles
Intraoperative and postoperative pain values between these three groups will be compared.
intrafen 800 mg
ibuprofen 800 mg in normal saline 150 cc before operation will be given in 30 minutes. Intraoperative and postoperative pain values between these three groups will be compared.
Other:
plasebos
normal saline 150 cc before operation will be given in 30 minutes. Intraoperative and postoperative pain values between these three groups will be compared.

Locations

Country Name City State
Turkey Erzincan University Erzincan

Sponsors (1)

Lead Sponsor Collaborator
Erzincan University

Country where clinical trial is conducted

Turkey, 

References & Publications (5)

Buvanendran A, Kroin JS. Multimodal analgesia for controlling acute postoperative pain. Curr Opin Anaesthesiol. 2009 Oct;22(5):588-93. doi: 10.1097/ACO.0b013e328330373a. Review. — View Citation

Hariharan S, Moseley H, Kumar A, Raju S. The effect of preemptive analgesia in postoperative pain relief--a prospective double-blind randomized study. Pain Med. 2009 Jan;10(1):49-53. doi: 10.1111/j.1526-4637.2008.00547.x. — View Citation

Jerjes W, El-Maaytah M, Swinson B, Banu B, Upile T, D'Sa S, Al-Khawalde M, Chaib B, Hopper C. Experience versus complication rate in third molar surgery. Head Face Med. 2006 May 25;2:14. — View Citation

Oscier CD, Milner QJ. Peri-operative use of paracetamol. Anaesthesia. 2009 Jan;64(1):65-72. doi: 10.1111/j.1365-2044.2008.05674.x. Review. — View Citation

Trampitsch E, Pipam W, Moertl M, Sadjak A, Dorn C, Sittl R, Likar R. [Preemptive randomized, double-blind study with lornoxicam in gynecological surgery]. Schmerz. 2003 Jan;17(1):4-10. German. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary intraoperative pain as assessed by visual analogue scale Assessment of Preemptive intravenous ibuprofen on intraoperative analgesic efficacy in 3. molar tooth extraction 5 month
Secondary postoperative pain as assessed by visual analogue scale postoperative analgesic contribution of preemptively administered intravenous ibuprofen. 5 month
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