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Clinical Trials/NCT07158541
NCT07158541RecruitingNot Applicable

An RCT Comparing Tunneled Coronally Advanced Flap (TCAF) and Modified Tunnel Technique (MTUN) in Combination With a Soft Tissue Graft for Single Recession Coverage

University Hospital, Ghent1 site in 1 country24 target enrollmentStarted: August 25, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
24
Locations
1
Primary Endpoint
mean root coverage

Study Overview

Brief Summary

Multiple techniques can be used for recession coverage. The most common techniques for single recessions are : tunnel technique (T) and coronally advanced flap (CAF) both combined with a palatal graft to provide sufficient gingival thickness. Recently two modifications have been described in literature, namely the tunneled coronally advanced flap and the modified tunnel. MTUN will function as the control group while people treated with the TCAF technique will function as the test group.

This randomized controlled trial compares MTUN and TCAF to determine which technique provides better root coverage for receding gums at single recession in the premandible. The main question it aims to answer is:

- What is the average root coverage achieved with each technique in the short and long term? This may be clinically relevant because covering gum recession can reduce tooth sensitivity, improve aesthetics and make oral hygiene easier.

Researchers will compare the modified tunnel technique (MTUN = the gum is undermined) with the tunneled coronally advanced flap (TCAF = the gum is undermined, only partially detached and repositioned higher). In both techniques, a small piece of tissue is removed from the palate, which is used to cover the recession. The purpose of the connective tissue graft under the flap/tunnel, is to increase thickness and provide support. Pain associated to the material used to cover the donorsite will be seen as the secondary research question. The site will either be covered by spongostan and multiple stitches or a palatal stent.

Participants will:

  • Undergo surgery (MTUN or TCAF, randomly assigned) to cover recessions
  • Attend regular check-ups for up to 10 years after surgery
  • Keep a postoperative journal (recording medication use, pain levels, tooth sensitivity, etc.)

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •at least 18 years old
  • •good oral hygiene
  • •presence of one recession in the premandible
  • •good general health

Exclusion Criteria

  • •pregnant women (assessed at each visit; if the patient appears pregnant during follow-up, x-rays will not be taken)

Arms & Interventions

MTUN + CTG

Active Comparator

Modified tunnel with connective tissue graft.

Intervention: modified tunnel with connective tissue graft (Procedure)

TCAF + CTG

Active Comparator

Tunneled coronally advanced flap with a connective tissue graft.

Intervention: tunneled coronally advanced flap with connective tissue graft (Procedure)

Outcomes

Primary Outcomes

mean root coverage

Time Frame: From enrollment up to ten years after surgical treatment.

The average percentage of previously exposed tooth root surface that becomes covered by gingival tissue following a root coverage procedure.

Secondary Outcomes

  • width of keratinized tissue(From enrollment up to ten years after surgical treatment.)
  • willingness to retreat(From three months post-operative up to two years post-operative.)
  • complete root coverage(From enrollment up to ten years after surgical treatment.)
  • pocket depth(From enrollment up to ten years after surgical treatment.)
  • recession reduction(From enrollment up to ten years after surgical treatment.)
  • width of keratinized tissue(From enrollment up to ten years after surgical treatment.)
  • gingival thickness(From enrollment up to ten years after surgical treatment.)
  • phenotype(From enrollment up to ten years after surgical treatment.)
  • treatment time(Only measured during surgery in minutes.)
  • post-operative pain at the donor site(From one week post-operative up to three months post-operative.)
  • number of analgesics(From one week post-operative up to two weeks post-operative.)
  • post-operative pain at the recession site(From one week post-operative up to three months post-operative.)
  • willingness to retreat(From three months post-operative up to two years post-operative.)
  • score of aesthetic result(From six months post-operative up to ten years post-operative.)
  • root sensitivity(From one week pre-operative up to ten years post-operative.)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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