PRF in surgery of impacted wisdom teeth of the lower jaw in contact with the nerve.
Conditions
Interventions
Intervention 1: Intervention group: In the intervention group, a 10cc blood sample is taken by a trained nurse before surgery and placed in a test tube that does not contain any substance. Then, the t
Sponsors
Mazandaran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: Patients who have at least one of their impacted or partially impacted wisdom tooth roots in contact with the inferior alveolar nerve canal. Patients without uncontrolled systemic problems who fall into ASA classification 1 and 2.
Exclusion criteria
Exclusion criteria: Age below 18 years and above 45 years The possibility of iatrogenic damage to the nerve during surgery Patients with acute pericoronitis and severe pain before surgery Patients taking antidepressant drugs Patients who consume more than 10 cigarettes per day Patients taking any medication that interferes with nerve, muscle and bone repair Horizontal tooth whose crown is very close to the nerve Patients taking osteoporosis drugs such as alendronate Patients with a history of radiotherapy and chemotherapy, less than 1 year has passed since their treatment history
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain, tingling, or numbness of the chin or lower lip, measured by the project manager based on the patient's description and the definition of paresthesia and anesthesia. Timepoint: All patients are examined at 6 hours, 24 hours, 72 hours, and one week after surgery. Patients are followed up for changes in chin and lip sensation at one-month, three-month, and six-month intervals. Method of measurement: Paresthesia is measured by the project manager based on the patient's description and the definition of paresthesia and anesthesia. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAida Karimzadehkan
Mazandaran University of Medical Sciences
Outcome results
None listed