Gingival Hyperpigmentaion Clinical Trial
Official title:
Ascorbic Acid Versus Diode Laser in the Treatment of Gingival Hyperpigmentation: Histological and Clinical Randomized Study
Verified date | August 2017 |
Source | Ain Shams University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Vitamin C affect the melanocytes function not the number while diode laser cause melanocytes destruction. Although diode laser and vitamin C have proved their effectiveness in depigmentation in previous studies, there are no published studies compared the effect of diode laser and vitamin C on melanocytes and melanosomes clinically and histologically.
Status | Completed |
Enrollment | 10 |
Est. completion date | September 10, 2016 |
Est. primary completion date | September 10, 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 40 Years |
Eligibility |
Inclusion Criteria: - Male and female patients with age ranging from 18 years old to 40 years old. - Bilaterally symmetric gingival hyperpigmentation on the maxillary and mandibular labial keratinized gingiva between canines. - Patients free from any systemic diseases as evidenced by the health questionnaire, using modified Cornell medical index (Pendleton et al., 2004). - Patients with thick gingival biotype = 3 mm. Exclusion Criteria: - Presence of local condition that may cause gingival hyperpigmentation (traumatized epithelium caused by defective fixed prosthesis or restoration). - Smokers. - Pregnant or lactating females. - Patients with poor oral hygiene, incompliance to treatment and persistence gingival inflammation after phase I periodontal therapy. - Clinically diagnosed periodontitis (attachment and bone loss, presence of periodontal pockets, gingival recession and tooth mobility). - Previous treatment to pigmentation. - Patients taking supplementary vitamin C for any reason. - Known sensitivity to ascorbic acid or any of its derivatives. - Patients taking any drug that may cause gingival pigmentation. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Ain Shams University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Dummett oral pigmentaion index (DOPI) | scoring from 0 ( no pigmentation to 3 (sever pigmentation | change from baseline to 1, 3 and 6 months | |
Primary | gingival brightness (?L) | using spectrophotometer | change from baseline to 1, 3 and 6 months | |
Primary | histological mean area fraction of melanosomes | by taking soft tissue samples and stained by fontana masson stain | change from baseline to 6 months | |
Secondary | patient satisfaction questionnaire | from scoring patients pain and cosmetic changes | immediate postopearive, 1 week, 1 month and 6 months |