Coronally Advanced Flap With Alloderm Versus Coronally Advanced Flap With Micro-needling on RT1 Gingival Recession

Sponsor
Cairo University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05470660
Collaborator
(none)
20
1
2
10
2

Study Details

Study Description

Brief Summary

This study aims to assess the effect of micro-needling together with coronally advanced flap procedure on the gain of gingival thickness (GT) and keratinized tissue width (KTW) and compare it to Alloderm with coronally advanced flap procedure in the management of thin periodontal phenotype associated with recession type 1 (RT1)

Condition or Disease Intervention/Treatment Phase
  • Procedure: Root coverage using coronally advanced flap combined with micro-needling
  • Procedure: coronally advanced flap combined with Alloderm
N/A

Detailed Description

Gingival or periodontal diseases were found to occur more likely in patients with a thin gingival biotype. The periodontal phenotype was also found to show stronger correlation with gingival thickness rather than keratinized tissue width and papilla height. Moreover, the thin gingiva was usually found to be associated with thin bony plate with potential for dehiscence and fenestration and hence was thought to be at risk for recession after trauma.

Several techniques have been recommended for the treatment of gingival recession. One of the most predictable outcome is associated with the use of a coronally advanced flap and acellular dermal matrix graft.

Treatment of thin periodontal phenotype through the conjunction of i-PRF and micro-needling may be a first move of the non-surgical approach for improving the gingival thickness. Micro-needling was proved to be generally an effective and safe therapeutic option for numerous dermatologic conditions as clinical improvement of scars, striae, and rhytids with appropriate recovery and limited side effects. The controlled dermal wounding and stimulation of the wound healing cascade through Micro-needling was found to enhance collagen production and thus was responsible for the clinical results obtained.

Therefore, this study will be aiming to compare the effect of micro-needling on the gingival thickness in root coverage procedures. It will also provide an insight of its effect on the patient related factors and the root coverage parameters.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
The Effect of Coronally Advanced Flap With Acellular Dermal Matrix (Alloderm) Versus Coronally Advanced Flap With Micro-needling on RT1 Gingival Recession: A Pilot Study
Anticipated Study Start Date :
Aug 1, 2022
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Jun 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Root coverage using coronally advanced flap combined with micro-needling

modified coronally advanced flap will be performed in sites of recession defects, then micro-needling will be performed after 1 month from the coronally advanced flap procedure to ensure the initial flap healing

Procedure: Root coverage using coronally advanced flap combined with micro-needling
modified coronally advanced flap will be performed in sites of recession defects, then micro-needling will be performed after 1 month from the coronally advanced flap procedure to ensure the initial flap healing.

Active Comparator: coronally advanced flap combined with Alloderm

modified coronally advanced flap will be performed in sites of recession defects in Association with alloderm to cover the exposed root and 3 mm of connective tissue mesial and distal to it.

Procedure: coronally advanced flap combined with Alloderm
modified coronally advanced flap will be performed in sites of recession defects in Association with alloderm to cover the exposed root and 3 mm of connective tissue mesial and distal to it.

Outcome Measures

Primary Outcome Measures

  1. Gingival thickness (GT) in mm [6 months]

    Gingival thickness (GT) will be specified at a mid-buccal location approximately 1 mm apical to the probing depth (PD) level with a #15 endodontic spreader. The reamer will be pierced, perpendicularly to the mucosal surface, through the soft tissue with light pressure until a hard surface is felt. The silicone disk stop will then be placed in tight contact with the soft tissue surface and fixed by a drop of cyanoacrylate adhesive; after careful removal of the reamer, penetration depth will be measured with a caliper to the nearest 0.1 mm gingival thickness changes will be calculated after 6 months

Secondary Outcome Measures

  1. Keratinized tissue width (KTW) in mm [6 months]

    Keratinized tissue (KT) will be measured from the most apical point of the gingival margin to the mucogingival junction measurements will be recorded at baseline and after 6 months

  2. Clinical Attachment Level (CAL) in mm [6 months]

    Will be measured from the Cemento-enamel Junction to the bottom of the gingival sulcus at baseline and 6 months

  3. Gingival Recession Depth (RD) in mm [6 months]

    Will be measured from the Cemento-enamel Junction to the most apical extension of the gingival margin.

  4. Gingival Recession Width (RW) in mm [6 months]

    Will be measured horizontally between the borders of the recession at the level of Cemento-enamel Junction.

  5. Percentage of root coverage [6 months]

    Preoperative vertical recession - Postoperative vertical recession/preoperative vertical recession) x 100.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Patient consulting in the outpatient clinic.

  • Able to tolerate the study procedures.

  • Patient ready to perform oral hygiene instructions.

  • Compliance with the maintenance program.

  • Provide informed consent.

  • Accepts the 6 months follow-up period

  • Mature permanent tooth.

  • Full-mouth plaque index (PI) and full-mouth bleeding on probing (BOP) score of ≤ 15%.

  • Presence of identifiable Cemento-enamel Junction.

  • RT1 facial recession defect of ≥3 mm.

  • Clinical indication and/or patient request for recession coverage

Exclusion Criteria:
  • Medically compromised patients.

  • use of any drugs that might lead to gingival enlargement

  • Pregnant or nursing women.

  • Uncooperative patients.

  • Smokers.

  • Teeth with malocclusion, crowding, fillings, missing or supernumerary mandibular anterior teeth.

  • Cairo Recession Type 3 (RT3) recession defects.

  • Teeth with active orthodontic treatment.

  • Previous periodontal surgery.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Faculty of Dentistry - Cairo University Cairo Egypt

Sponsors and Collaborators

  • Cairo University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Salma Ossama Ezzat Moursy, principle investigator. Salma Ezzat, Cairo University
ClinicalTrials.gov Identifier:
NCT05470660
Other Study ID Numbers:
  • PER331
First Posted:
Jul 22, 2022
Last Update Posted:
Jul 22, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Salma Ossama Ezzat Moursy, principle investigator. Salma Ezzat, Cairo University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 22, 2022