CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 20 enrolled
Drug / intervention
Autologous fat grafting +1 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04214041
NCT04214041N/ACompleted
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Soft Tissue Volume Augmentation of Localized Horizontal Ridge Defects Using Autologous Fat Grafting Versus Subepithelial Connective Tissue Graft (a Randomized Controlled Clinical Trial)

Nourhan M.Aly·interventional·Posted Dec 30, 2019·Updated Dec 4, 2023

In Brief

A clinical study evaluating Autologous fat grafting and Sub-epithelial connective tissue graft for Alveolar Bone Loss. Completed, enrolled 20 participants across 1 site.

Detailed Summary

The aim of this study was to evaluate the effectiveness of autologous fat as a grafting material for soft tissue volume augmentation of localized horizontal ridge defects in humans.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAlveolar Bone Loss
CountriesEgypt
CollaboratorsAlexandria University

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedDec 30, 2019
Enrollment StartDec 17, 2018
Primary CompletionJun 25, 2019
Study CompletionSep 11, 2019
TodayJul 2, 2026
Enrollment to primary: 6 monthsPosted 6.5 years ago

Interventions

Autologous fat graftingother

A fat graft will be aspirated from the abdomen under local anaesthesia and processed using the Microfat grafting technique. Afterwards the fat graft will be injected in the previously created pouch at the recipient site. Then the pouch will be closed using interrupted sutures 5-0 vicryl.

Sub-epithelial connective tissue graftother

A subepithelial connective tissue graft of a size that corresponds to that of the defect will be harvested from the palate using the trap door technique. The donor site will be closed using cross horizontal sling sutures and interrupted sutures 4-0 vicryl. Subsequently, the graft will be inserted in the previously created pouch at the recipient site and secured to the flap using vicryl sutures 5-0. Then the pouch will be closed using interrupted sutures.