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Clinical Evaluation of Laterally Closed Tunnel Technique Versus Coronally Advanced Flap Combined With Connective Tissue Graft for the Treatment of Isolated RT2 Gingival Recession

Clinical Evaluation of Laterally Closed Tunnel Technique Versus Coronally Advanced Flap Combined With Connective Tissue Graft for the Treatment of Isolated RT2 Gingival Recession: A Randomized Controlled Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05823415
Enrollment
22
Registered
2023-04-21
Start date
2023-04-30
Completion date
2024-03-31
Last updated
2023-04-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Recession, Gingival

Brief summary

The aim of this study is to evaluate reduction of recession depth using lateral closed tunnel technique versus CAF technique using connective tissue graft in single RT2 gingival recession cases.

Interventions

PROCEDURELaterally Closed Tunnel with CTG

A novel minimally invasive surgical approach laterally closed tunnel technique (LCT) has been recently introduced for the management of isolated gingival recession. The laterally closed tunnel technique ensures predictability by tunneling and mobilization of flap for graft coverage.

PROCEDURECAF with CTG

Gold standard surgical technique

Sponsors

British University In Egypt
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Single RT2 buccal gingival recession ≥ 2 mm in the esthetic zone (Gingival recession associated with loss of inter-proximal attachment. The amount of interproximal attachment loss (measured from the interproximal CEJ to the depth of the interproximal pocket) was less than or equal to the buccal attachment loss (measured from the buccal CEJ to the depth of the buccal pocket) * Patients with good oral hygiene * Medically free patients * No signs of active periodontal disease (with no site showing probing depth \> 4 mm and full-mouth bleeding score (FMBS) 20% (measured at four sites per tooth). * Palate with sufficient thickness to accommodate soft tissue defect.

Exclusion criteria

* Smokers * Pregnancy * Severe gag reflex * Non-carious cervical lesion * History of mucogingival or periodontal surgery at the experimental site * History of medication that can affect periodontal healing

Design outcomes

Primary

MeasureTime frame
Reduction in recession depth6 Months

Secondary

MeasureTime frameDescription
Probing Depth6 months
Clinical Attachment Level6 monthswill be measured by a periodontal probe
Post-operative pain assessed by VAS Scale2 weekPain score reported by the patient directly through Visual Analogue Scale score (between 0 and 10, 0: no pain, 1: minimal pain 5: moderate pain, 10: severe pain)
Gingival Thickness6 months
Percentage of complete root coverage by williams periodontal probe6 monthsPreoperative vertical recession - Postoperative vertical recession/preoperative vertical recession) x 100
Width of Keratinized Tissue6 months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026