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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05679453
Other study ID # 10
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date July 20, 2022
Est. completion date September 29, 2022

Study information

Verified date December 2022
Source Kutahya Health Sciences University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Our study aimed to compare the effect of lornoxicam and etodolac on postoperative pain, edema and trismus following lower third molar extraction


Description:

20 patients included in study (4 male, 16 female). Lornoxicam and etodolac was given following lower third molar extraction. Pain was evaluated 2., 6., 12., 24., and 48. hours using VAS. Edema was evaluated by measuring tragus-labial commissure, angulus- lateral canthus of eye and angulus mandible-labial commissure. Trismus was evaluated measuring mouth opening by caliper. Edema and Trismus was evaluated by 48. and 168. hours


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date September 29, 2022
Est. primary completion date September 25, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: - Bilateral mesioangular impacted lower third molar - Asymptomatic Third Molar (No history of infection) - Systemically Healthy Person - Person Between aged 18-30 Exclusion Criteria: - People who are pregnant and lactation process - People who had any systemic disease - People who are gastrointestinal problems - People who are sensitive to drugs used in study - Lower Third Molar associated with cysts and infections

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Lornoxicam 8 Mg Oral Tablet
Lornoxicam is a oxicam grup non-steroid antiinflamatuar drug

Locations

Country Name City State
Turkey Zülfikar Karabiyik Kutahya

Sponsors (1)

Lead Sponsor Collaborator
Kutahya Health Sciences University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain after wisdom tooth extraction Pain after lower third molar removal, Pain was evaluated with VAS(visual anolog scale) 2 th hours
Primary Edema after wisdom tooth extraction Edema lower third molar removal, Edema was evaluated by using reference line on the face 48 th hours
Primary Trismus after wisdom tooth extraction Trismus lower third molar removal, trismus was evaluated by using caliper 48 th hours,
Secondary Pain after wisdom tooth extraction Pain after lower third molar removal, Pain was evaluated with VAS(visual anolog scale) 6 th hours
Secondary Pain after wisdom tooth extraction Pain after lower third molar removal, Pain was evaluated with VAS(visual anolog scale) 12 th hours
Secondary Pain after wisdom tooth extraction Pain after lower third molar removal, Pain was evaluated with VAS(visual anolog scale) 24 th hours
Secondary Pain after wisdom tooth extraction Pain after lower third molar removal, Pain was evaluated with VAS(visual anolog scale) 48 th hours
Secondary Edema after wisdom tooth extraction Edema lower third molar removal, Edema was evaluated by using reference line on the face 168 th hours
Secondary Trismus after wisdom tooth extraction Trismus lower third molar removal, trismus was evaluated by using caliper 168 th hours
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