Amnion Membrane Versus DFGG Using the Tunneling Technique in Management of Gingival Recession Defects.

Sponsor
Cairo University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06146855
Collaborator
(none)
22
1
2
11.3
1.9

Study Details

Study Description

Brief Summary

Treatment of gingival recession is indicated mainly for esthetic reasons and keratinized tissue augmentation (Zucchelli and Mounssif, 2015). An array of surgical techniques has been proposed by the literature to cover gingival recession defects with well-documented successful outcomes. The selection of one technique over the other depends on many factors. Some of these factors are related to the gingival recession defect itself, others are related to the anatomy of the palatal fibromucosa, or related to the patient variabilities (Zucchelli and De Sanctis, 2000).

Controversy exists in the literature regarding the patient morbidity after connective tissue graft harvesting. Inconclusive postulations have been made about the post-operative patient morbidity outcomes and root coverage outcomes when comparing connective tissue graft harvesting in comparison to allograft membranes used for root coverage.

The use of connective tissue graft in combination with root coverage techniques remain the gold standard for root coverage procedures. The problem with the connective tissue graft is that harvesting a graft from the palate increases morbidity, needs an extra surgical site which is more traumatic for the patient, depends on the donor tissue which could be limited, increases surgical chair-time and needs increased surgical skills (Cortellini & Pini Prato 2012).

The rationale behind the use of amnion membrane is to avoid the morbidity inherent with connective tissue graft harvesting.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Tunneling procedure with Amnion Membrane
  • Procedure: Tunneling procedure with De-epithelialized Free Gingival Graft
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
22 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Amnion Membrane as a Soft Tissue Substitute Versus De- Epithelialized Free Gingival Graft Using the Tunneling Technique in Management of Gingival Recession Defects: A Randomized Controlled Clinical Trial.
Anticipated Study Start Date :
Nov 22, 2023
Anticipated Primary Completion Date :
Nov 1, 2024
Anticipated Study Completion Date :
Nov 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Tunneling with amnion membrane

Procedure: Tunneling procedure with Amnion Membrane
Root Coverage by tunneling procedure with the addition of Amnion Membrane as a soft tissue substitute

Active Comparator: Tunneling with De-epithelialized Free Gingival Graft

Procedure: Tunneling procedure with De-epithelialized Free Gingival Graft
Root Coverage by tunneling procedure with the addition of De-epithelialized Free Gingival Graft

Outcome Measures

Primary Outcome Measures

  1. Recession depth [3-6 month]

    Measured from the CEJ to the most apical extension of the gingival margin.

Secondary Outcome Measures

  1. Recession width [3-6 month]

    Measured horizontally between the borders of the recession.

  2. Percentage of root coverage [6 months]

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

  3. Root coverage esthetic score [6 months]

    Based on Cairo et al., (2009) the root coverage esthetic score (RES) system evaluated five variables 6 months following surgery: gingival margin (GM), marginal tissue contour (MTC), soft tissue texture (STT), MGJ alignment, and gingival color (GC).

  4. Gingival Thickness [3-6 months]

    Determined 2 mm apical to the gingival margin with a short needle for anesthesia and a 3 mm diameter silicon disk stop. The needle is inserted perpendicular to the mucosal surface, through the soft tissues with light pressure until a hard surface is felt. The silicon disk stop is then placed in tight contact with the soft tissue surface with the coronal border overlapping the soft tissue margin. As the needle is located in the center of the silicon disk, measurement of GT is performed 2 mm apical from the gingival margin. After careful removal of the needle, the penetration depth is measured with a caliper accurate to the nearest 0.1 mm (Paolantonio et al., 2002; da Silva et al., 2004; Joly et al., 2007).

  5. Keratinized tissue width [3-6 months]

    Measured as the distance between the gingival margin and the mucogingival junction (MGJ).

  6. Post-Operative Pain [1 week]

    Visual Analogue Scale (VAS) with numbers from 0 to 10 ('no pain' to 'worst pain imaginable') measured daily for the first week postoperatively.

  7. Post-Surgical Patient Satisfaction [1 week]

    A 3-item questionnaire is asked and the patients shall use a 7- point answer scale. (Kiyak et al., 1984)

  8. Surgical time [intraoperative]

    Total time of the surgical procedure measured using a stopwatch.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Age between 18 and 60 years.

  • Periodontally and systemically healthy.

  • Presence of RT1 or RT2 buccal gingival recession defects ≥2 mm in depth.

  • Full-mouth plaque and bleeding score of <15% and no probing depths >3 mm.

  • Absence of non-carious cervical lesions (NCCLs) and non-detectable cemento-enamel junction (CEJ) at the defect sites.

Exclusion Criteria:
  • RT3 recession defects.

  • Smokers as smoking is a contraindication for any plastic periodontal surgery (Khuller, 2009).

  • Presence of caries lesions or restorations in the cervical area.

  • Intake of medications which impede periodontal tissue health and healing.

  • Medical contraindications for periodontal surgical procedures.

  • Uncooperative patients not willing to complete the follow up period.

  • Pregnancy and lactation.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Faculty of Oral and Dental Medicine Cairo Egypt 12114

Sponsors and Collaborators

  • Cairo University

Investigators

  • Principal Investigator: Mohamed Mashaly, MSc, Assistant lecturer of Periodontology, Cairo University
  • Study Chair: Noha Ghallab, Phd, Professor of Oral Medicine and Periodontology, Cairo University
  • Study Director: Weam El Battawy, Phd, Assistant Professor of Oral Medicine and Periodontology, Cairo University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Mohamed Mashaly, Assistant lecturer of Periodontology, Cairo University
ClinicalTrials.gov Identifier:
NCT06146855
Other Study ID Numbers:
  • AMvsDFGG
First Posted:
Nov 27, 2023
Last Update Posted:
Nov 27, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 27, 2023