Malocclusion, Pain, Acute
Conditions
Keywords
Orthodontics, RANK-L, Ketorolac, Paracetamol, Gingival crevicular fluid
Brief summary
Due to the high prevalence of malocclusions in Mexico and the existing concern to improve aesthetics, function (chewing), or both, patients resort to orthodontic treatment. The patient may experience pain during treatment due to the release of different chemical mediators such as RANK-L. Analgesic and anti-inflammatory medications such as acetaminophen and ketorolac are used to control pain during orthodontic tooth movement. These drugs can inhibit the expression of RANK-L which can affect tooth movement, inhibiting bone remodeling. The orthodontist should indicate the drug that is safest for the patient without affecting treatment or tooth movement.
Detailed description
Objective: To evaluate the association of RANK-L levels with the administration of paracetamol and ketorolac in patients starting orthodontic treatment. Material and methods: A double-blind clinical trial will be carried out with a placebo control group and random drug allocation. Patients who begin orthodontic treatment in the Orthodontic Specialty of the Comprehensive Dental Clinics of the University Center for Health Sciences and who decide to participate in the study with the signing of informed consent will be included. Three groups will be formed with 8 patients in each one. The first group will be administered with Placebo (calcined magnesia), the second group with Ketorolac and the third group with Paracetamol, for all groups the medication will be one capsule every 6 hours for 5 days all study subjects will be sampled Gingival Crevicular Fluid (LGC), Visual Analogue Pain Scale (APS) and Intermolar Space (IS). Measurements will be made four times; baseline, 24 h, 48 h, and on day 5 of initiation of treatment.
Interventions
DRUGKetorolac
The first group will be administered with Placebo (calcined magnesia), the second group with Ketorolac and the third group with Paracetamol, for all groups the medication will be one capsule every 6 hours for 5 days all study subjects will be sampled Gingival Crevicular Fluid (LGC), Visual Analogue Pain Scale (APS) and Intermolar Space (IS).
Sponsors
University of Guadalajara
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Caregiver, Investigator)
Masking description
Blinded, the orthodontist performing the clinical intervention and the investigator
Intervention model description
A double-blind clinical trial will be carried out with a placebo control group and random drug allocation. Patients who begin orthodontic treatment in the Orthodontic Specialty of the Comprehensive Dental Clinics of the University Center for Health Sciences and who decide to participate in the study with the signing of informed consent will be included. Three groups will be formed with 8 patients in each one. The first group will be administered with Placebo (calcined magnesia), the second group with Ketorolac and the third group with Paracetamol, for all groups the medication will be one capsule every 6 hours for 5 days all study subjects will be sampled Gingival Crevicular Fluid (LGC), Visual Analogue Pain Scale (APS) and Intermolar Space (IS).
Eligibility
Sex/Gender
ALL
Age
18 Years to 27 Years
Healthy volunteers
Yes
Inclusion criteria
* Patients of both sexes between 18 and 27 years of age * Periodontally and systematically healthy * Attended the Orthodontic Clinic of the University of Guadalajara * Who required the use of dental spacers in at least one quadrant were included
Exclusion criteria
* Patients who have previously had orthodontic treatment or are under orthodontic treatment * Who have an allergy to ketorolac or paracetamol * Who are under pharmacological treatment and/or using contraceptives * Pregnant or lactating women, as well as those who consume alcohol were not included or tobacco.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Leves RANK-L | Baseline, 24 hours, 48 hours, and on day 5 of initiation of treatment. | Leves Gingival Crevicular Fluid of RANK-L |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Pain scale | Baseline, 24 hours, 48 hours, and on day 5 of initiation of treatment. | Visual Analogue Pain Scale (APS) |
| Intermolar Space (IS) | 5 days of initiation of treatment. | It is the space between the molars |
Countries
Mexico
Contacts
Primary ContactJUAN RAMÓN GÓMEZ, PhD
Backup ContactJUAN RAMÓN GÓMEZ, PhD
Outcome results
None listed