Guided Creeping Technique (GCT) in Treating Gingival Recession

Sponsor
October 6 University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05101642
Collaborator
Ain Shams University (Other)
12
1
1
8.5
1.4

Study Details

Study Description

Brief Summary

A novel minimally invasive guided creeping technique (GCT) is suggested to treat gingival recessions.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Guided Creeping Technique (GCT)
N/A

Detailed Description

Background: Coronally advanced flap with connective tissue grafting in a conventional or minimally invasive approaches includes massive soft tissue reflection that reduce soft tissue support and compromise vascularity around the grafted material. In an attempt to preserve soft tissue support, graft stability and maximizing graft protection in treating recession defects the present novel minimally invasive guided creeping technique (GCT) is suggested.

Methods: Twelve patients, each contributing a single Cairo RT1 GR defect, were treated by guided creeping technique and completed the 6 months follow up. Clinical, evaluations were performed and differences among groups were analyzed.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
12 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Guided Creeping Technique (GCT) as a Novel Minimally Invasive Approach in Treating Gingival Recession - Single Arm Preliminary Study
Actual Study Start Date :
Sep 15, 2021
Anticipated Primary Completion Date :
Jun 1, 2022
Anticipated Study Completion Date :
Jun 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Guided Creeping Technique (GCT)

Novel minimally invasive guided creeping technique

Procedure: Guided Creeping Technique (GCT)
Guided Creeping Technique (GCT) is a novel minimally invasive blind tunnel

Outcome Measures

Primary Outcome Measures

  1. Recession Coverage [Change from baseline to 6 months]

    Measured in mm

Secondary Outcome Measures

  1. Keratinized Tissue Width [Change from baseline to 6 months]

    Measured in mm

  2. Keratinized Tissue Thickness [Change from baseline to 6 months]

    Measured in mm

Other Outcome Measures

  1. Patient Reported Outcome [Through 14 days]

    Visual Analog Scale (VAS)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Over 18 years of age

  • Systemically and periodontally healthy

  • Presence of isolated buccal Cairo RT1 gingival recessions

  • An identifiable CEJ

  • Affected teeth with at least 2mm attached gingiva.

Exclusion Criteria:
  • Smokers

  • Pregnancy

  • Using antiepileptic drugs

  • Using antibiotics for at least 20 days before surgery

Contacts and Locations

Locations

Site City State Country Postal Code
1 October 6 University Giza Egypt 1211

Sponsors and Collaborators

  • October 6 University
  • Ain Shams University

Investigators

  • Principal Investigator: Ahmed Y Gamal, Professor, Faculty of Dentistry, October 6 University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ahmed Y Gamal, Professor of Periodontology, October 6 University
ClinicalTrials.gov Identifier:
NCT05101642
Other Study ID Numbers:
  • 4-21
First Posted:
Nov 1, 2021
Last Update Posted:
Nov 1, 2021
Last Verified:
Oct 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ahmed Y Gamal, Professor of Periodontology, October 6 University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 1, 2021