Skip to main content
Clinical Trials/NCT04258696
NCT04258696UnknownNot Applicable

Assessment of Lateral and Vertical Tissue Displacement Obtained by the Retraction Cord and Diode Laser

Cairo University1 site in 1 country22 target enrollmentStarted: June 30, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
22
Locations
1
Primary Endpoint
Amount of lateral tissue displacement

Study Overview

Brief Summary

In fixed prosthodontic treatment, deflection of gingival tissues for diagnosis or making an impression is one of the important phases. Gingival displacement is defined as "displacement of gingival tissues both in vertical and lateral dimensions". Lateral retraction displaces the tissues so that an adequate bulk of impression material can be interfaced with the prepared tooth. Vertical retraction exposes the uncut portion of the tooth apical to the finish line Conventional gingival retraction cord technique may injure the healthy epithelial lining and result in postoperative gingival recession The diode laser has been used for displacing gingiva to make a definitive impression. Rather than displacing gingival tissue, it removes the epithelial lining from the sulcus.

The aim of the Study is to compare between the Ultrapak retraction cord and diode laser regarding the amount of vertical and lateral retraction and patient comfort.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
20 Years to 45 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age range of the patients from 20-45 years old; able to read and sign the informed consent document, illiterate patient will be avoided.
  • •Patients able physically and psychologically to tolerate conventional restorative procedures.
  • •Patients with no active periodontal disease.
  • •Patients with thick gingival biotype.
  • •Patients with teeth problems indicated for full coverage restoration .
  • •Vital or non vital teeth.
  • •Good Oral hygiene.

Exclusion Criteria

  • •Patients with poor oral hygiene.
  • •Patients with thin gingival biotype.
  • •Pregnant women.
  • •Unmotivated patients.
  • •Patients with gingival recession.
  • •Patients with psychiatric problems or unrealistic expectation .
  • •patient suffer from parafunctional habit .
  • •Smokers and heavy caffeine consumers.

Arms & Interventions

Gingival retraction by ultrapak retraction cord

Active Comparator

Intervention: ultrapak Knitted retraction cord (Device)

Gingival retraction by diode laser

Experimental

Intervention: diode laser (Device)

Outcomes

Primary Outcomes

Amount of lateral tissue displacement

Time Frame: through study completion,up to 24 weeks

Measured using Stereomicroscope

Secondary Outcomes

  • Amount of vertical tissue displacement(through study completion,up to 24 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Alaa Abdelzaher Abdelhamid Omara

Lecturer assistant , Fixed Prosthodontics Department ,Faculty of Dentistry

Cairo University

Study Sites (1)

Loading locations...

Similar Trials

Assessment of Lateral and Vertical Tissue... | Clinical Trial