Faculty of Dentistry Cairo University
Cairo, Egypt
Location status: Recruiting
NCT Number: NCT06577285
Participants with esthetic concern of excessive gingival display who meets the inclusion criteria, will be carried out including history taking, clinical examination and initial therapy.
The initial therapy will consist of periodontal treatment (phase I therapy) including supragingival scaling, subgingival debridement if needed. The mechanical plaque control instructions for each patient include brushing and interdental cleaning techniques. Patients who have inadequate crown length and width ratio or short clinical crown will receive esthetic crown lengthening procedure to adjust gingival levels before being included in this study.
Patients in the intervention group I will take zinc gluconate 50 mg 1 per day to increase zinc level with phytase supplement 176mg (800FTU) 2 tablets per day to give the maximum absorption of zinc, both supplements will be given for 4 days before botulinum toxin injections. Patients in the intervention group II will take zinc gluconate 50 mg 1 per day to increase zinc level, 4 days before botulinum toxin injections.
Patients in the control group will receive the Botulinum toxin injections only Clinical photographs will be taken at baseline, 2 weeks, 1 month, 3 months postoperatively.
Interested in participating?
Request Info18 year–60 year
All sexes
Interventional
Not applicable
Cairo, Egypt
Location status: Recruiting
Initial examination:
Participants with esthetic concern of excessive gingival display who meets the inclusion criteria, will be carried out including history taking, clinical examination and initial therapy.
The initial therapy will consist of periodontal treatment (phase I therapy) including supragingival scaling, subgingival debridement if needed. The mechanical plaque control instructions for each patient include brushing and interdental cleaning techniques.
Preoperative procedures:
Patients who have inadequate crown length and width ratio or short clinical crown will receive esthetic crown lengthening procedure to adjust gingival levels before being included in this study.
Clinical photographs:
Clinical photographs will be taken at baseline, 2 weeks, 1 month, 3 months postoperatively.
Intervention group I:
Patients in the intervention group I will take zinc gluconate 50 mg (Now food company) 1 per day to increase zinc level with phytase supplement 176mg (800FTU) (Goodphyte company) 2 tablets per day to give the maximum absorption of zinc, both supplements will be given for 4 days before botulinum toxin injections.
Intervention group II:
Patients in the intervention group II will take zinc gluconate 50 mg (Now food company) 1 per day to increase zinc level, 4 days before botulinum toxin injections.
Control group:
Patients in the control group will receive the Botulinum toxin injections only.
Botulinum toxin type A injection:
The patients will be injected at both sides into the "Yonsei point," (3Units) the point that would target 3 muscles responsible for upper lip elevation during smiling, including the levator labii superioris alaeque nasi (LLSAN), in a single injection. This landmark will be identified as the center of a triangle formed by the convergence of the LLSAN, the levator labii superioris (LLS), and the Zygomaticus minor muscles and is located 1 cm lateral to the ala horizontally and 3 cm above the lip line vertically in both men and women (Hwang et al. 2009) and (Nasr et al. 2015).
Postoperative care:
After Botox injection the patients will be instructed to:
Follow up:
Botox will gradually take effect over 7-10 days with optimum result at 2 weeks. After 2 weeks the patients would come for an additional touch up dose (1 unit at each injection point)
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
zinc gluconate 50 mg1 per day with phytase supplement 176mg (800FTU) (Goodphyte company) 2 tablets per day
zinc gluconate 50 mg 1 per day, 4 days before botulinum toxin injections.
Time frame: The gingival display will be measured at baseline, 2 weeks, 4 weeks, 2 months, 3 months.
To measure the amount of gingival display, a digital camera will be used to take the close up perioral as well as frontal smiling photographs. Care will be taken to capture a nonposed spontaneous smile. A measuring scale with ruler will be used for standardization of the photographs.
Time frame: 2 weeks, 3 months
Will be measured by using questionnaire using Likert scale
Time frame: baseline, 2 weeks and 3 months
The compound muscle action potential is an electromyography investigation that measures the simultaneous action potentials for a group of muscle fibers in the same area
Time frame: baseline, 2 weeks and 3 months:
Classification by (Rubin 1974) according to neuromuscular smile pattern
Three main types:
The commissure smile: Mona Lisa smile, where the corners of the mouth are pulled up and outward followed by the levators of the upper lips contracting to show the upper teeth.
The cuspid (canine) smile: The levator labii superioris are dominant. They contract first, exposing the canine teeth. The corners of the mouth contract secondarily to pull the lips upward and outward.
The complex smile: all the elevators of the lips, the elevators of the corners of the mouth, and the depressors of the lower lips contract at the same time to show all the upper and lower teeth
Time frame: baseline, 2 weeks and 3 months:
A group of 12 dentists will evaluate the before and after photographic records and rate the results on a 1 to 5 point scale.
Contact information is provided by the study sponsor or research team.
Mawda M Hussain, Bachelor
CONTACT
Nesma F Shemais, lecturer
CONTACT
Cairo University
Other
The Effect Of Botulinum Toxin A In Patients With Excessive Gingival Display With And Without Zinc And Phytase Supplementation: A Randomized Clinical Trial
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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