Skip to main content
Clinical Trials/NCT07649226
NCT07649226Enrolling By InvitationNot Applicable

Laser-Assisted Minimally Invasive Esthetic Crown Lengthening Using Flapless vs. Tunneled Flap Approach (Randomized Controlled Clinical Trial)

Alexandria University1 site in 1 country45 target enrollmentStarted: March 30, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Enrolling By Invitation
Enrollment
45
Locations
1
Primary Endpoint
leukocyte esterase enzyme assessment using Periomonitor

Study Overview

Brief Summary

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 Design

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

Eligibility Criteria

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

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

Arms & Interventions

conventional surgical crown lenhthening

Active Comparator

gold standard of treatment

Intervention: surgical esthetic crown lengthening (Procedure)

Laser assissted flapless approach

Active Comparator

Intervention: laser assissted crown lengthening (Procedure)

Tunneled flap approach

Active Comparator

Intervention: Laser-assisted tunneled flap approach (Procedure)

Outcomes

Primary Outcomes

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

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.

PROM

Time Frame: 1 week

Binary questionnaire (Yes/No) questions will be asked.

Secondary Outcomes

  • Marginal bone loss evaluated using CBCT(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials

Laser-Assisted Minimally Invasive Esthetic... | Clinical Trial