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

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04258696
Enrollment
22
Registered
2020-02-06
Start date
2020-06-30
Completion date
2020-12-30
Last updated
2020-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Broken Teeth Injury With Complication, Endodontically-Treated Teeth, Spacing of Anterior Maxillary Teeth

Keywords

Gingival retraction, Gingival displacement, Diode laser

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.

Interventions

DEVICEdiode laser

using Ultrapak Knitted retraction cord as a gingival retraction method . using Wiser Cordless Dental Diode Laser from Doctor Smile Dental Laser By LAMBDA SpA Italy as a gingival retraction method.• The tip of diode laser, will be angled toward the soft tissue and away from the prepared tooth, will be passed along the gingival sulcus to remove the sulcular epithelium. Constant and steady short brushing strokes gently removed the lining of the sulcus in order to achieve a full 360-degree trough. The tip will be constantly cleaned with a gauze sponge wetted with hydrogen peroxide to remove debris and to eliminate potential bacterial contamination. sufficient epithelium will be removed to place the impression material and visualize the finishing line. The tissue will be kept moist with water during the procedure then impression will be taken

DEVICEultrapak Knitted retraction cord

using Ultrapak Knitted retraction cord as a gingival retraction method retraction cord will be applied for 8-10 mins then an impression will be taken , poured to obtain a cast and the die sectioned

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 45 Years
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.

Design outcomes

Primary

MeasureTime frameDescription
Amount of lateral tissue displacementthrough study completion,up to 24 weeksMeasured using Stereomicroscope

Secondary

MeasureTime frameDescription
Amount of vertical tissue displacementthrough study completion,up to 24 weeksMeasured using Stereomicroscope

Other

MeasureTime frameDescription
Patient satisfactionthrough study completion,up to 24 weeksPain scale ( 0 - 5 ) 5 means maximum pain, worse outcome , 1 means low pain,better outcome o means no pain

Countries

Egypt

Contacts

Primary ContactAlaa Omara, M.D.s
alaa.abdelzaher@dentistry.cu.edu.eg01025238079
Backup ContactOmaima Elmahalawy, professor
01222154399

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026