CClinicalTrials.gg
Active, not recruitingNCT06044870Updated Oct 2, 2025

Clinical Evaluation of the Modified Laterally Stretched Technique (RT2) Gingival Recession vs Tunneling With CT Grafting

An interventional study of Modified laterally stretched technique with a connective tissue graft. in Gingival Recession, sponsored by Cairo University. Active, not recruiting at 1 site in Egypt. Open to participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-10-02.

Sponsored by Cairo University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Oct 2025, 1 year ago, but the record still lists the study as active, not recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
26
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study summary

Regression analysis in a recent systematic review showed significantly greater mRC and CRC values when modifications are done to the TUN procedure to achieve more coronal advancement of the flap, coronal advancement also helps in covering the underlying graft for better recession coverage outcomes (Tavelli et al., 2018), limited data is present on the possible influence of a covered or partially uncovered graft. However, it has been suggested that minimal exposure of the CTG may aid not only in achieving CRC but also a harmonious gingival margin (John et al., 2015; Rasperini et al., 2011).

02

Conditions studied

  • Gingival Recession

Browse trials for

03

In context

Gingival Recession

402 studies on the registry are indexed under Gingival Recession; 98 are open to participants now.

This study's enrollment of 26 is below the median of 30 across 368 interventional studies indexed under Gingival Recession.

Browse Gingival Recession studies →

Lead sponsor

Cairo University is the lead sponsor of 4,780 studies on the registry; 1,427 are open to participants now.

Of its 36 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

  • Single or multiple RT2 gingival recession site/sites in the lower anterior teeth.
  • Age >/= 18 years.
  • Patients with healthy or treated periodontal conditions.
  • Patients willing to participate in the study.
  • Absence of uncontrolled medical conditions.
  • Full mouth plaque score \</= 20% (O'Leary 1972).
  • Full mouth bleeding score \<20% (Ainamo and Bay 1975).
  • Patients with aesthetic concerns.

Exclusion Criteria:

  • Pregnant or lactating females.
  • deep recession sites more than 5 mm
  • Tobacco smoking.
  • Uncontrolled medical conditions.
  • Uncooperative patients or unable to complete the study.
  • Patients treated with any medication known to cause gingival hyperplasia.
  • No occlusal interferences.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
26 participants (actual)

Study arms

  • Experimental
    Modified laterally stretched technique with a connective tissue graft.

    After the administration of local anesthesia, root planing of the exposed root surfaces will be performed by means of hand instruments. A partial thickness envelope is performed with tunneling instruments involving one or two teeth adjacent to the tooth, in case of a very thin biotype a complete thickness envelope could be done. Two horizontal incisions are done at the base of the papillae of the deepest recession site, allowing to place the graft in a more coronal position and improving access and visibility.

    Procedure: Modified laterally stretched technique with a connective tissue graft.

  • Active comparator
    Tunneling technique with connective tissue graft.

    Immediately before surgery, contact point composite stops were placed to prevent the collapse of the suspended sutures in the inter-proximal spaces.• The entire gingival papillary complex will be moved coronally using a suspended suture anchored in the lingual gingiva (Aroca et al., 2010, 2013; Azzi et al, 2002, zuhr et al.,2009).

    Procedure: Modified laterally stretched technique with a connective tissue graft.

Interventions

  • ProcedureModified laterally stretched technique with a connective tissue graft.

    Modified laterally stretched technique with a connective tissue graft.

06

What researchers measure

Primary outcomes

  1. Recession depth reduction.

    Measured as the difference between the recession gingival depth at different follow up intervals and the baseline.

    Time frame: 1 year

Secondary outcomes

  1. Mean root coverage

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

    Time frame: 1 year

  2. Recession depth

    Measured as the distance between the free gingival margin and the cemento-enamel junction .

    Time frame: 1 year

  3. Recession width

    Measured as the distance between the between the mesial gingival margin and distal gingival margin

    Time frame: 1 year

  4. Soft tissue thickness

    The measurement of Gingival tissue thickness is performed 2 mm apical from the gingival margin.

    Time frame: 1 year

  5. Keratinized tissue width

    Measured as the distance between the gingival margin and the muco-gingival junction.

    Time frame: 1 year

  6. Esthetics (RES) score

    A system used to evaluate five variables 6 months gingival margin (GM), marginal tissue contour (MTC), soft tissue texture (STT), MGJ alignment, and gingival color (GC).

    Time frame: 1 year

  7. patient satisfaction

    A 3-item questionnaire is asked, and the patients shall use a 7-point answer scale. The answers were given on a 7-point scale ranging from 1 'not at all'' to 7 ''very likely''.

    Time frame: 1 year

07

Study locations

1 site
  • Cairo University
    Cairo, Egypt
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 2, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06044870
Lead sponsor
Cairo University
Responsible party
Maha fawzy el sayed ali abd allah (assistant lecturer, Cairo University) — Principal investigator
First posted
Sep 21, 2023
Start date
Sep 1, 2023
Primary completion
Oct 2025 (estimated)
Completion
Nov 2025 (estimated)
Last update
Oct 2, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Oct 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion