Actively Recruiting
Clinical Evaluation of Different Treatments for Interdental Black Triangles
Led by Ain Shams University · Updated on 2026-04-23
30
Participants Needed
1
Research Sites
25 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This randomized clinical trial aims to evaluate and compare the effectiveness of surgical and nonsurgical treatment approaches for the management of interdental black triangles. Black triangles are open gingival embrasures caused by the loss or deficiency of the interdental papilla between adjacent teeth. These spaces are a common esthetic concern and may also contribute to food impaction and periodontal problems. Thirty adult patients presenting with interdental papillary loss classified as Nordland and Tarnow Class I or II will be recruited from the outpatient clinics of the Faculty of Dentistry at King Salman International University. Eligible participants will be randomly assigned to one of three treatment groups: surgical reconstruction using the tube grafting technique, papillary augmentation using hyaluronic acid injection, or a restorative approach using the injection molding composite technique. Clinical and photographic assessments will be performed at baseline and during follow-up visits at 3 and 6 months after treatment. The primary outcomes will be the reduction in black triangle surface area and height. Secondary outcomes will include clinical periodontal parameters such as plaque index, bleeding score, probing pocket depth, and clinical attachment level. Patient satisfaction with the esthetic outcome will also be evaluated using a Visual Analog Scale (VAS). The findings of this study are expected to provide evidence regarding the comparative effectiveness of surgical and nonsurgical approaches for the management of interdental black triangles and help clinicians select the most predictable treatment modality for improving esthetic outcomes.
CONDITIONS
Official Title
Clinical Evaluation of Different Treatments for Interdental Black Triangles
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 to 50 years
- Interdental black triangle classified as Nordland and Tarnow Class I or II
- Adequate interdental bone support (≤5 mm from contact point to alveolar crest) confirmed by X-ray
- Systemically healthy with no medical conditions affecting wound healing
- Willingness to participate and attend follow-up visits at 3 and 6 months
You will not qualify if you...
- Systemic diseases that may impair wound healing
- Teeth with acute periapical pathology
- Presence of periodontal pockets or active periodontal disease
- Pregnant or lactating women
- Parafunctional habits such as bruxism
- Smokers, alcoholics, or drug abusers
AI-Screening
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Trial Site Locations
Total: 1 location
1
Faculty of Dentistry, King Salman International University
Cairo, Egypt
Actively Recruiting
Research Team
F
Fatma E.A. Hassanein, PHD
CONTACT
F
Fatma E.A. Hassanein, PHD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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