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Pontic Site Development With Connective Tissue Graft Using Modified Pouch Technique Versus Pouch Technique

NCT03882216 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2019-03-20

No results posted yet for this study

Summary

The study will be formed on two groups : the control group and the test group For both groups base line impressions will be taken before the surgery and a free gingival graft will be harvested from the palate and deepithelialized to obtain the free connective tissue graft then In the control group: the free connective tissue graft will be inserted through crestal pouch previously prepared using split thickness flap.

In the test group The free connective tissue graft will be slided through apical vertical incision in the pontic area previously tunneled.

Post operative casts will be obtained by taking impressions after three months and six months to evaluate the volumetric changes in the pontic area.

Conditions

  • Ridge Deficency
  • Soft Tissue Augmentation

Interventions

PROCEDURE

soft tissue augmentation using pouch technique

crestal incision with split thickness flap without vertical releasing incision till the mucogingival line then apply the harvested connective tissue graft through it.

PROCEDURE

soft tissue augmentation using modified pouch technique

tunneling will be done at the pontic site till the mucogingival line then a distant vertical incision near the tunnel at the lining mucosa where the harvested connective tissue graft wll be applied .

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-06-20
Primary Completion
2021-12-31
Completion
2022-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03882216 on ClinicalTrials.gov