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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT02975024 |
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Date of registration:
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16/11/2016 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Blood Flow Analysis of the Human Mucosa After Vestibuloplasty Procedures
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Scientific title:
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Date of first enrolment:
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November 2016 |
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Target sample size:
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8 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02975024 |
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Study type:
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Observational |
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Study design:
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Phase:
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Countries of recruitment
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Hungary
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Contacts
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Name:
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Janos Vag |
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Address:
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Telephone:
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Email:
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Affiliation:
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Semmelweis University, Dept. of Conservative Dentistry |
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Key inclusion & exclusion criteria
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Ages Eligible for Study: 18 Years to 45 Years Genders Eligible for Study: Both Accepts
Healthy Volunteers: Yes
Inclusion Criteria:
• clinical diagnosis of inadequate width of keratinized gingiva at the mandibular front
region
Exclusion Criteria:
- pregnancy
- heavy smoking
- general diseases
- taking medications or having treatments which have an effect on mucosal healing in
general (e.g. steroids, anti-inflammatory drugs)
- taking any other medications in the last three months (except contraceptives)
Age minimum:
18 Years
Age maximum:
45 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Mucogingival Defect
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Intervention(s)
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Device: wound fluid measurement
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Device: laser speckle contrast imaging of the oral mucosa
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Device: quantitative determination of VEGF
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Primary Outcome(s)
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Postoperative blood flow changes of the oral mucosa
[Time Frame: 6 months after surgery]
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Secondary Outcome(s)
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Quantitative determination of Vascular Endothelial Growth Factor (VEGF) of the wound fluid
[Time Frame: 4 days after surgery]
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Evaluation of the periodontal parameters at teeth at the surgical site: a composite outcome measure consisting of multiple measures.
[Time Frame: Pre- and six month postoperative]
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Wound fluid volume measurement
[Time Frame: 14 days after surgery]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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