Evaluation of the Modified VISTA Technique Using ALB-PRF vs CTG in the Treatment of Multiple Miller Class III Recessions

NCT ID: NCT06643507

Last Updated: 2024-11-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

PHASE2/PHASE3

Total Enrollment

26 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-11-20

Study Completion Date

2026-01-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

treatment of miller class III RT2 gingival recession using modified vista technique using connective tissue graft vs albumin PRF

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

treatment of gingival recession is an important element in the treatment of periodontitis this study covers clinical evaluation of using the modified VISTA technique with using Albumin-PRF VS connective tissue graft in the treatment of miller class III / RT2 for root coverage outcomes

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Gingival Recession

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

patients with gingival recession control group

patients with gingival recessions of miller class III /RT2 the control group will be treated with modified vista technique using connective tissue graft

Group Type ACTIVE_COMPARATOR

Connective tissue graft

Intervention Type OTHER

regenerative properties

patients with gingival recession interventional group

patients with gingival recessions of miller class III /RT2 the interventional group will be treated with modified vista technique using albumin PRF

Group Type EXPERIMENTAL

ALB-PRF

Intervention Type BIOLOGICAL

regenerative properties

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Connective tissue graft

regenerative properties

Intervention Type OTHER

ALB-PRF

regenerative properties

Intervention Type BIOLOGICAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* 18 years old good oral hygiene

Exclusion Criteria

* smokers patients with poor oral hygiene
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Cairo University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Tamani Mahmoud Abdullah Fakhri

clinical evaluation of the modified VISTA technique (M-VISTA)using Albumin -platelet rich fibrin (Alb-PRF)versus connective tissue graft (CTG)in the treatment of multiple miller class III/RT2recessions : a randomized clinical trial

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Enji EA Ahmed, BDS.MDS.PHD

Role: STUDY_DIRECTOR

Cairo University

Sarah SE Elbanna, BDS.MDS.PHD

Role: STUDY_DIRECTOR

Cairo University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Faculty of Dentistry Cairo University

Cairo, , Egypt

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Tamani TM Mahmoud, BDS.MDS

Role: CONTACT

Egypt:+201017874915

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Cairo C.U university

Role: primary

010 02159535

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

PER 3 -3 -1

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.