Investigating the effect of suture technique on treatment outcomes following mandibular third molar dental surgery

Not Applicable

Recruiting

• Conditions: Impacted tooth.; Impacted teeth; K01.1

• Registration Number: IRCT20180515039664N3
• Lead Sponsor: Zahedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 15 June 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Existence of mandibular third molar with the degree of latency A and B and class I and II (based on Pell & Gregory classification)
Informed consent to participate in the study
surgery with hardness grades 2 and 3 and the maximum difference between the two sides in terms of degree of hardness and classification 1 and in terms of trauma surgery on both sides in the same way.

Exclusion Criteria

Existence of any systemic disease
Existence of decay
pregnancy or lactation
Take any coagulation medication

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: 1st, 3rd, 7th, and 15th day after surgery. Method of measurement: VAS pain scale.;Swelling. Timepoint: 1st, 3rd, 7th, and 15th day after surgery. Method of measurement: Clinical examination.;Trismus. Timepoint: 1st, 3rd, 7th, and 15th day after surgery. Method of measurement: Clinical examination.