Teeth, Impacted Clinical Trial
Official title:
Usefulness of Amelogenins in the Treatment of Periodontal Defects on the Distal Surface of the Lower Second Molar After Adjacent Third Molar Extraction: a Pilot Study
Verified date | March 2020 |
Source | University of Roma La Sapienza |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Background: Prevention of periodontal defects after the extraction of lower third molars
remains a challenge. Various methods have been proposed in the literature, but there are no
studies which evaluated the effectiveness of amelogenins.
Methods: A single-blind split-mouth randomized controlled clinical trial (RCT) was performed
on 5 patients to verify if amelogenins had some benefits in improving lower second molar
periodontal healing after adjacent third molar extraction. A PPD ≥ 8 mm associated with a
radiographic bone defect of at least 5 mm were the main inclusion criteria.
Status | Completed |
Enrollment | 5 |
Est. completion date | April 20, 2018 |
Est. primary completion date | April 20, 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 27 Years |
Eligibility |
Inclusion Criteria: - Patients aged < 27, for which the extraction of both lower third molars was indicated - Bilateral total (bone or osteo-mucosal) third molar impaction - Bilateral bone defect = 5mm distal to the lower second molars, evaluated on pre- operative periapical radiographs performed with Rinn's film holders - PPD = 8mm distal to the second lower molars, in at least one of the following probing sites: buccal, disto-buccal, disto-central, disto-lingual - Intra-operative integrity of both third molar buccal and lingual alveolar cortices Exclusion Criteria: - Smoking habit - Systemic disorders with serious immunologic impairment - Taking cortisone or other drugs that might interfere with healing process - Allergy to penicillins - Previous periodontal treatment - Less than 2 mm of adherent gingiva at second molar level - Second molars with a prosthetic crown - Previous endodontic treatment of second molars - Furcation involvement of the second molars |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University of Roma La Sapienza |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | CAL (Clinical attachment level) pre operative | baseline, pre-surgery | ||
Primary | CAL (Clinical attachment level) post operative | 7 days after surgery | ||
Primary | CAL (Clinical attachment level) 3 months | 3 months after surgery. | ||
Primary | CAL (Clinical attachment level) 12 months | 12 months after surgery. | ||
Primary | PPD (Periodontal probing dept) pre operative | baseline, pre-surgery | ||
Primary | PPD (Periodontal probing dept) post operative | 7 days after surgery | ||
Primary | PPD (Periodontal probing dept) 3 months | 3 months after surgery. | ||
Primary | PPD (Periodontal probing dept) 12 months | 12 months after surgery. | ||
Primary | REC (recession) pre operative | baseline, pre-surgery | ||
Primary | REC (recession) post operative | 7 days after surgery | ||
Primary | REC (recession) 3 months | 3 months after surgery. | ||
Primary | REC (recession) 12 months | 12 months after surgery. | ||
Primary | Radiographic bone Level pre operative | An endoral x-ray was taken baseline, pre-surgery | ||
Primary | Radiographic bone Level post operative | An endoral x-ray was taken 7 days after surgery | ||
Primary | Radiographic bone Level 3 months | An endoral x-ray was taken 3 months after surgery. | ||
Primary | Radiographic bone Level 12 months | An endoral x-ray was taken 12 months after surgery. | ||
Secondary | Adverse Events pre operative | the occurrence of adverse events after the use of amelogenins. | pre-operative | |
Secondary | Adverse Events post operative | the occurrence of adverse events after the use of amelogenins. | 7 days after surgery | |
Secondary | Adverse Events 3 months | the occurrence of adverse events after the use of amelogenins. | 3 months after surgery. | |
Secondary | Adverse Events 12 months | the occurrence of adverse events after the use of amelogenins. | 12 months after surgery. |
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