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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06148961
Other study ID # 2023-2025
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date February 1, 2024
Est. completion date October 30, 2025

Study information

Verified date January 2024
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The growing interest of patients in esthetic procedures, as well as the development of less invasive protocols in dentistry, has promoted the development of treatment plans that include stability, harmony, and function in orofacial rehabilitation. Poor esthetics interfere with an individual's personal, social, and professional relationships and is an individual consideration that varies according to the patient's age, time, region, and culture concerning what is considered beautiful.


Description:

People are increasingly being inspired to get more corrective and cosmetic surgeries as an esthetic smile becomes a more fundamental component of what it means to be beautiful. There are several variables that affect how appealing and esthetic a smile is Esthetic perception varies according to cultural, societal, environmental, and individual factors like experience and educational level Previous studies have shown that a smile with less gingival display (GD) is viewed as more beautiful, with dental professionals being more critical of gingival presentation than laypeople According to research by several authors, the ideal GD ranges from 1 to 3 mm While many factors influence how pleasant a smile is seen, excessive GD (EGD), sometimes referred to as a gummy smile, is regarded as a key factor in smile analysis and one of the main issues connected to an unsatisfactory dental smile. To reduce the relapse associated with repositioning surgery and to provide a lasting treatment without the need for reapplication, as in the case of the toxin, a combined treatment using the toxin preoperatively was considered.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date October 30, 2025
Est. primary completion date June 30, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - Patients that is not satisfied with his smile having excessive gingival display - Adult Age = 21 years. - Systemically and periodontally Healthy patients. - had gingival exposure greater than 3 mm when smiling - had a hyperactive upper lip with or without other causes of EGD (lip displacement = 9 mm) before botox & = 3mm after. - Cooperative patients able and accept to come for follow up appointments. Exclusion Criteria: - • smoking - pregnancy or lactation - Systemic diseases; neuromuscular,neurological, or psychological disorders or consumption of controlled medication - Patients having medical condition or any drugs that could affect healing - Patients with systemic condition that can't undergo minor oral surgery - Patient allergic to Botox or multiple allergic conditions - have history of previous Botox injection - periodontal disease - excessive gingival display at rest - those who declined the informed consent or who did not consent to the risks described. - Those who have deviate smile

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
botox prior to modified lip repostioning
botox injection prior to surgical intervention by 5 to 10 days A surgical marker was used to outline the boundaries of the surgical incision region. the height of the superior incision was measured as 15 mm within the vestibule. Superior and inferior incisions were made with a scalpel blade number 15 and linked bilaterally by two vertical incisions. A partial thickness dissection was used to remove the strip of the indicated mucosa, exposing the fascia of the connective tissue beneath. When necessary, all salivary glands and frenal attachments were removed. The surgical site was then properly closed using a periosteal simple interrupted suture was put in place prior to the continuous interlocking sutures. It was placed by commencing the needle 2 mm coronal to Per surgery site, 3 to 4 periosteal sutures were typically The new mucosal boundary to the gingiva was stabilized in its new place using this suture

Locations

Country Name City State
Egypt Cherine Emad Mahmoud Mohamed Hamada Giza

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Other Maintenance of reduction of gingival display callipper 3 , 6 & 12 months
Primary Change in gingival display Using a 15-cm marked ruler (Antunes et al., 2022) 3,6&12 months
Secondary Patient's satisfaction Survey (Silva et al., 2013) 3,6 &12 months
See also
  Status Clinical Trial Phase
Not yet recruiting NCT06075134 - EMG-guided Botox Injection Versus Conventional Botox Injection in Gummy Smile Patients N/A
Recruiting NCT06017791 - Management of Excess Gingival Display Using Tunnel Technique With 3D Designed PEEK Shell: A Case Series N/A
Completed NCT03717987 - The Effect of Botulinum Toxin A In Patients With Excessive Gingival Display With And Without Zinc Supplementation Phase 3