Clinical Trials Directory

Trials / Unknown

UnknownNCT05383820

Effect of Paracetamol and Ketorolac on RANK-L Levels in Patients Starting Orthodontic Treatment

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
24 (estimated)
Sponsor
University of Guadalajara · Academic / Other
Sex
All
Age
18 Years – 27 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGKetorolacThe 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).

Timeline

Start date
2021-09-27
Primary completion
2022-03-10
Completion
2022-12-18
First posted
2022-05-20
Last updated
2022-05-20

Locations

1 site across 1 country: Mexico

Source: ClinicalTrials.gov record NCT05383820. Inclusion in this directory is not an endorsement.