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NCT03413553

Clinical Evaluation of Soft Tissue Augmentation Using CTG and PRF Around Immediately Placed Dental Implants Versus Immediate Implant Alone in Esthetic Zone .

Completed NA Last updated 3 August 2021
What this trial tests

NA trial testing immediate implant in Soft Tissue Augmentation in 20 participants. Completed in 15 January 2020.

Timeline
1 March 2018
Primary endpoint
30 September 2019
15 January 2020

Quick facts

Lead sponsorAbeer hassan sharafuddin
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment20
Start date1 March 2018
Primary completion30 September 2019
Estimated completion15 January 2020
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Abeer hassan sharafuddin — full company profile →

Who can join

Adults 18 to 50, any sex, with Soft Tissue Augmentation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The main hypothesis to be certified is that the addition of Subepithelial Connective Tissue Graft (SCTG) and Platelet rich Fibrin (PRF) to immediately placed implants will not significantly differ from immediately placed implant alone as regard gingival tissue stability.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of immediate implant

Trials testing the same drug.

Other recruiting trials for Soft Tissue Augmentation

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03413553.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing