Oral Surgery Clinical Trial
Official title:
Randomized Clinical Trial of Microbial Growth in the Suture Thread, After the Post-surgical Application of Different Antiseptic Gels in Mandibular Third Molars Extraction
Verified date | June 2017 |
Source | University of Santiago de Compostela |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is a randomized clinical trial in which investigators will compare the antimicrobial
effect and inducer of cicatrization as well as the degree of postoperative pain in patients
who are extracted the lower third molars.
After the surgery, different bioadhesive gels will be applied in the area of the surgical
wound and we will evaluate the aforementioned parameters.
Status | Completed |
Enrollment | 21 |
Est. completion date | September 10, 2014 |
Est. primary completion date | July 15, 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 39 Years |
Eligibility |
Inclusion Criteria: - Age: between 18 and 39 years. - Good general health. - Availability during the study. - No current odontological treatments or foreseen during the study period. - Acceptance and compliance with the prescribed oral hygiene instructions. - Agreement to not used mouthwashes or toothpastes with antiseptic agents during the study period. Exclusion Criteria: - Use of antimicrobial mouthwashes or toothpastes during the period during which the suture remains in the mouth. - Diabetes. - Smoking. - Degenerative diseases. - Deficient oral health (cavities, periodontal disease, pathologies of the oral mucosa...). - Wearing prosthetic or orthodontic devices. - Amoxicillin allergy. - Pregnant or lactating women. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University of Santiago de Compostela |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Microbiological growth on suture tread. | Microbiological growth in CFUs on the suture thread after the application of the distinct bioadhesive gels. | Seven days. | |
Primary | Postoperative pain in the operated area. | The researchers will analyze the degree of postoperative pain patients suffered during the first postoperative week by applying one of the gels to be studied in the area of the surgical wound. To make this measurement the visual analogue pain scale will be used. | Seven days. | |
Primary | Degree of healing. | The degree of healing at 7 days after surgery was measured using a visual healing scale consisting of four different levels of healing status: - Erithymatous surgical zone and with signs of inflammation and infection. - Erythematous surgical site without signs of infection. -Surgical zone of normal color and beginning of epithelization. -Surgical zone of normal color and advanced epithelization. |
Seven days. |
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