Soft Tissue Profile Following Socket Preservation With Platelet Rich

Clinical Trial Description

Extraction of the non restorable tooth, then socket preservation is applied in experimental group using platelet rich fibrin, while in comparative group free gingival graft is applied with socket preservation. ;

Study Design

Related Conditions & MeSH terms

Soft Tissue Mass

See also
Status	Clinical Trial	Phase
Completed	`NCT03452644` - US-Guided Biopsy in the Diagnosis of Musculoskeletal Soft-Tissue Tumors
Completed	`NCT03667261` - Using Sealing Socket Abutment Technique With Immediate Implant in the Mandibular Molars	N/A
Recruiting	`NCT05355597` - "The Efficacy of Exparel Versus a Multidrug Cocktail in Soft Tissue Tumors"	Phase 2

See also

Status

Clinical Trial

Phase

Completed

NCT03452644 - US-Guided Biopsy in the Diagnosis of Musculoskeletal Soft-Tissue Tumors

Completed

NCT03667261 - Using Sealing Socket Abutment Technique With Immediate Implant in the Mandibular Molars

N/A

Recruiting

NCT05355597 - "The Efficacy of Exparel Versus a Multidrug Cocktail in Soft Tissue Tumors"

Phase 2

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT03628170
Study type	Interventional
Source	Cairo University
Contact	Haya Hesham, Masters
Phone	01272789994
Email	shaimaanasr@live.com
Status	Recruiting
Phase	N/A
Start date	June 7, 2018
Completion date	February 2019

Soft Tissue Profile Following Socket Preservation With Platelet Rich Fibrin Versus Free Gingival Graft

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms