- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07649226
Laser-Assisted Minimally Invasive Esthetic Crown Lengthening Using Flapless vs. Tunneled Flap Approach
June 12, 2026 updated by: Alexandria University
Laser-Assisted Minimally Invasive Esthetic Crown Lengthening Using Flapless vs. Tunneled Flap Approach (Randomized Controlled Clinical Trial)
Crown lengthening surgery is one of the most commonly performed periodontal procedures.
Multiple techniques have been used throughout the years to overcome the postoperative pain and adverse outcomes that may be associated with surgical crown lengthening.
One of the most popular choices among clinicians is using different types of lasers in different techniques to overcome those adverse effects.
Treatment effectiveness can be monitored non-invasively through salivary levels of Leukocyte Esterase enzyme and the stability clinical outcomes.
Study Overview
Status
Enrolling by invitation
Conditions
Study Type
Interventional
Enrollment (Estimated)
45
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Alexandria Governorate
-
Alexandria, Alexandria Governorate, Egypt
- Alexandria University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Patients with an excessive gingival display of at least 3 mm
- Age >21 years
- At least six anterior maxillary teeth requiring ECL
- Healthy periodontal status, indicated by a full-mouth plaque index and bleeding on probing index scores of <15%.
- Patients with thick gingival phenotype
Exclusion Criteria:
- Treatment sites with probing depths more than 3 mm
- Patients with a history of smoking
- Patients with a history of mucogingival surgery in the intended treatment area
- Systemic conditions that could hinder tissue healing (e.g., uncontrolled diabetes and autoimmune diseases)
- Patients undergoing active orthodontic treatment
- Presence of any cause of excessive gingival display other than altered passive eruption
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: conventional surgical crown lenhthening
gold standard of treatment
|
surgical crown lengthening using scalpels and rotary instruments.
|
|
Active Comparator: Laser assissted flapless approach
|
laser-assissted flapless crown lengthening and laser-assissted tunneled flap approach
|
|
Active Comparator: Tunneled flap approach
|
In this approach, the gingival margin will be tunneled to provide visibility for the operator during bone removal using laser.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
leukocyte esterase enzyme assessment using Periomonitor
Time Frame: 1 month
|
Periomonitor strips will be used to detect the amount of leukocyte esterase enzyme in saliva
|
1 month
|
|
Clinical outcome stability
Time Frame: 6 months
|
Clinical outcome stability will be assessed by measuring the length of the crown and interdental papillae immediately postoperatively, 1 week postoperatively, 1 month postoperatively, 3 months postoperatively and 6 months postoperatively.
|
6 months
|
|
PROM
Time Frame: 1 week
|
Binary questionnaire (Yes/No) questions will be asked.
|
1 week
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Marginal bone loss evaluated using CBCT
Time Frame: 6 months
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 30, 2026
Primary Completion (Estimated)
June 1, 2026
Study Completion (Estimated)
September 1, 2026
Study Registration Dates
First Submitted
June 4, 2026
First Submitted That Met QC Criteria
June 12, 2026
First Posted (Actual)
June 16, 2026
Study Record Updates
Last Update Posted (Actual)
June 16, 2026
Last Update Submitted That Met QC Criteria
June 12, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- 9296348
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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