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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06397521
Other study ID # 22879
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 20, 2024
Est. completion date December 31, 2024

Study information

Verified date April 2024
Source Ain Shams University
Contact Doaa Adel-Khattab, PhD
Phone 01006814258
Email dr.doaa.adel-khattab@dent.asu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In patients with excessive gingival display, esthetic crown lengthening procedure by means of scalpel, diode laser or electro-surgery could result in the same gingival marginal stability at 3 and 6 months follow up.


Description:

Scalpel crown lengthening has been recommended as the gold standard for treating excessive gingiva. Two other established tools used for gingivectomy procedures are electrosurgery and lasers. Laser crown lengthening may have the advantages of less bleeding during the procedure, faster healing, and less pain following the procedure. Electrosurgery which involves the application of a high- frequency electric current to the gingiva has been shown to produce minimal bleeding, ease and speed of cutting and reduced postoperative pain. The null hypothesis that the three techniques for aesthetic crown lengthening (ACLP) would show equivalent gingival margin stability at 3 and 6 months follow up.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 21
Est. completion date December 31, 2024
Est. primary completion date December 20, 2024
Accepts healthy volunteers No
Gender All
Age group 25 Years to 45 Years
Eligibility Inclusion Criteria: - Altered passive eruption as presence of quadratic anterior teeth [crown width/length ratio - 0.85 ]. - Gingival margin located coronal to the tooth cervical convexity and >2 mm of gingival band display during maximum smile. - Patients with treated periodontal disease (i.e., stage I of periodontitis); Exclusion Criteria: - Patients with systemic contraindications for oral surgery as uncontrolled diabetes. - patients on drug therapy related with drug-associated gingival enlargement. - Areas in which the remaining amount of keratinized gingiva after the submarginal incision is less than 3 mm. - Previous surgical treatment in the same area.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Crown lengthening
Investigation of the three techniques for aesthetic crown lengthening

Locations

Country Name City State
Egypt Doaa Adel Salah Khattab Cairo Abbassia

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary position of the gingival margin position of the gingival margin (GM) (Degree of Gingival Rebound) after performing an aesthetic crown lengthening procedure 3 and 6 months postoperative
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