The Effect of Functional Crown Lengthening Versus Deep Margin Elevation on Periodontal Tissues

ConditionTNF Alpha
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-50
SponsorAin Shams University

About this trial

The present study will evaluate and compare the effect of functional CL and DME in the treatment of posterior teeth with class II caries clinically and on the level of TNF-α in the GCF of treated teeth.

Clinical evaluation of periodontal tissue in the form of probing depth as a primary outcome, clinical attachment level, plaque index, bleeding index, gingival index, pink aesthetic score, Radiographic evaluation of biological width and the level of TNF-α in the GCF as a secondary outcome.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients aged 20-50 years

Both genders

Patients free from any systemic disease that may affect the treatment (Greenberg & Glick, 2012)

Patients with intact periodontium

Disqualifiers

Pregnant and lactating females

Smokers

Drug abusers.

Patients with persistent poor oral hygiene

Trial design

Design model

Parallel

Treatments tested in this trial

  • Functional Crown lengthening

    Procedure/Surgery

    patients will undergo functional crown lengthening by raising a full thickness flap with osseous resection to establish a distance of 3 mm between the cervical margin of the cavity and the bone crest. Osteoplasty was performed in the adjacent and neighboring tooth surfaces to accomplish a smooth bone contour. The flaps will then be sutured in their new position

  • Deep Margin Elevation

    Procedure/Surgery

    patients will undergo deep margin elevation through a two-step direct restoration performed using the concepts of Progressive Matrixing and Wedging where the Deep subgingival cavity margin will be acquired. Then isolation by rubber dam. A curved matrix will seal the margin without any gingival or rubber dam entrapped in between. One step adhesive system will be performed under rubber dam isolation. Composite resin base is applied to raise the margin by about 2 mm. A bulk fill packable or flowable composite can be used. Finishing will be done using polishing strips and disks. Finally a bitewing radiograph will be taken to check the presence of overhangs or gaps before the final restoration.

Treatment groups

20 Participants
are divided into 2 treatment groups
Group A: Functional crown lengtheningExperimental treatment 1 intervention
Group B: Deep Margin ElevationActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Probing depth

Will be measured from the gingival margin to the depth of the pocket at four points (mesio-facial, mid-facial, disto-facial and mid-lingual) to the nearest millimeter using UNC-15 periodontal probe. The average of the three facial points will be recorded as the facial probing depth (FPD), while the mid-lingual point will be recorded as the lingual probing depth.

Time frame
Clinical measurements preoperative and will be repeated at 1, 3, and 6 months

Secondary outcomes

1

Biochemical evaluation

GCF samples will be collected to measure the level of TNF-α in treated teeth. Before sampling, the adjacent teeth will be isolated with cotton rolls. Crevicular fluid will be collected on perio paper strips placed parallel to the long axis of the tooth of concern in the gingival sulcus until mild resistance is felt and kept for 30 seconds and pooled in reduced transport fluid (RTF) medium for biochemical analysis. GCF collected samples contaminated with blood and saliva will be discarded

Time frame
Biochemical measurements preoperative and will be repeated at 1, 3 and 6 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: