Skip to main content
Clinical Trials/NCT04192864
NCT04192864CompletedNot Applicable

Comparison Between the Lingually Based and the Buccally Based Triangular Flap Design in the Surgical Removal of Impacted Mandibular Third Molars (Randomized Split Mouth Clinical Trial)

Nourhan M.Aly1 site in 1 country20 target enrollmentStarted: October 25, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
20
Locations
1
Primary Endpoint
Postoperative Pain using Visual Analogue Scale (VAS)

Study Overview

Brief Summary

The primary objective of this study was to compare between the lingually based triangular flap with the buccally based triangular flap in the surgical removal of impacted mandibular third molars.

Detailed Description

Many flap designs used for impacted third molar surgery do not place the mucoperosteal incision on sound bone, as they involve incisions that are placed on the extraction socket resulting in higher incidence of mucosal dehiscence, followed by secondary wound healing

This study involved 20 patient with bilaterally mesially angulated impacted third molar (class II position B). One side was surgically removed using the lingually based triangular flap and the other side was surgically removed using the bucally based triangular flap

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
Single (Participant)

Masking Description

This study was a single blinded trial, where the participants did not know the technique used in each side.

Eligibility Criteria

Ages
21 Years to 30 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Presence of impacted third molar that is misally angulated and retained in bone (class II position B).

Exclusion Criteria

  • •Patients with a history of systemic disease (diabetes, renal failure, immunocompromised patients, cardiac patients and patients taking radiotherapy or chemotherapy )
  • •Compromised dental and periodontal status
  • •Heavy Smoking.
  • •Pregnancy or lactation

Arms & Interventions

Lingually based triangular flap

Experimental

Intervention: Lingually based triangular flap (Procedure)

Buccally based triangular flap

Active Comparator

Intervention: Buccally based triangular flap (Procedure)

Outcomes

Primary Outcomes

Postoperative Pain using Visual Analogue Scale (VAS)

Time Frame: 7 days

Pain was assessed through on a 10-point Visual Analogue Scale (VAS). (0-1= None, 2-4= Mild, 5-7= Moderate, 8-10= Severe)

Postoperative Edema

Time Frame: 7 days

For the objective evaluation of swelling, five distances were measured * The distance from the mandibular angle to the lateral corner of the mouth * The distance from the mandibular angle to the nasal alar curvature * The distance from the mandibular angle to the lateral canthus of the eye * The distance from the tragus to the soft tissue pogonion * The distance from the tragus to the lateral corner f the mouth

Trismus Assessment

Time Frame: 7 days

Trismus was assessed by measuring the maximum inter-incisional opening (in millimeters) the distance between the incisal edge of the upper and lower central incisor using caliber.

Wound healing/ Presence of alveolar osteitis

Time Frame: 21 days

The presence of alveolar osteitis (dry socket) will be determined clinically using BLUM'S criteria. Wound healing was assessed and recorded depending on the absence or presence of dehiscence, every opening along the incision will be recorded as dehiscence , dental tweezers will be used to identify it.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Nourhan M.Aly
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Nourhan M.Aly

Instructor of Dental Public Health

University of Alexandria

Study Sites (1)

Loading locations...

Similar Trials

Comparison Between the Lingually Based and... | Clinical Trial