Comparison of Innovative Suture with Conventional Suture on Severity of Complications Following Mandibular fully Impacted third molar Surgery

Not Applicable

• Conditions: Localized swelling, mass and lump, unspecified; Condition 1: Mandibular fully impacted third molar surgery. Condition 2: Postoperative facial swelling after mandibular fully impacted third molar surgery. Condition 3: Trismus after mandibular fully impacted third molar surgery. Condition 4: Dehiscence after mandibular fully impacted third molar surgery. Condition 5: Dry socket after mandibular fully impacted third molar surgery.; Impacted teeth; Sprain of jaw; Disruption of external operation (surgical) wound, not elsewhere classified; Alveolitis of jaws; T81.31

• Registration Number: IRCT20181021041404N1
• Lead Sponsor: Research center of Semnan Dental School

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 14 January 2019

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

Both-sided and symmetrical impaction of mandibular third molar tooth that are classified in the same class by Pell & Gregory
Meeting ASA1 systemic conditions
Non-smokers patients
Collaborative patients with frequent visits for follow up
Patients without periodontal disease
patients with proper oral hygiene
patients aged between 20 and 30

Exclusion Criteria

Pathologic lesion in the impacted tooth
Difference in follicle size around the crown of each person's sides
Surgical time exceeding 25 minutes
More than 5 minutes of surgical difference on both sides
Taking steroids, drugs, alcohol, contraceptives
Pregnancy and lactation
History of delayed wound healing
Failure to complete follow up sessions

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Before starting surgery, it is assessed that there is no pain at the surgical site.pain of the patient 12 hours after surgery and on days 7, 1, 2, 3, 4, 5, 6 after surgery will be measured. Method of measurement: Visual Analogue Scale.