Lornoxicam Versus Etodolac After Third Molar Surgery

NCT ID: NCT05679453

Last Updated: 2023-01-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-07-20

Study Completion Date

2022-09-29

Brief Summary

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

Detailed Description

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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

Conditions

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Pain, Acute Edema Trismus

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SEQUENTIAL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Lornoxicam

Lornoxicam, 8 mg twice per day for four days

Group Type ACTIVE_COMPARATOR

Lornoxicam 8 Mg Oral Tablet

Intervention Type DRUG

Lornoxicam is a oxicam grup non-steroid antiinflamatuar drug

Etodolac

Etodolac, 400 mg tid per a day for four days

Group Type ACTIVE_COMPARATOR

Lornoxicam 8 Mg Oral Tablet

Intervention Type DRUG

Lornoxicam is a oxicam grup non-steroid antiinflamatuar drug

Interventions

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Lornoxicam 8 Mg Oral Tablet

Lornoxicam is a oxicam grup non-steroid antiinflamatuar drug

Intervention Type DRUG

Other Intervention Names

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Etodolac

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Kutahya Health Sciences University

OTHER

Sponsor Role lead

Responsible Party

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Zulfikar Karabiyik

Research Assistant

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Zülfikar Karabıyık

Kütahya, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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10

Identifier Type: -

Identifier Source: org_study_id

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