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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04609748
Other study ID # KB-0012/149/2020
Secondary ID
Status Recruiting
Phase Phase 2
First received
Last updated
Start date January 27, 2021
Est. completion date December 31, 2021

Study information

Verified date January 2021
Source Pomeranian Medical University Szczecin
Contact Bartosz Dalewski, DMD, PhD
Phone 914661717
Email bartosz.dalewski@pum.edu.pl
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

During the study, the effectiveness of analgesic therapy with nimmsulide and cannabidiol oil will be compared. Two study groups will be formed. The study will be conducted on patients reporting to the Dental Prosthetics Clinic of PUM in Szczecin. Patients aged 18-65 years with pain located in the area of the temporomandibular joint and the preauricular area, resulting from a dysfunction of the temporomandibular joint, will be included in the study.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date December 31, 2021
Est. primary completion date July 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: 1. Patients (female and male) aged 18-65 years, able to swallow tablets 2. Patients with pain located in the temporomandibular and preauricular regions resulting from temporomandibular joint dysfunction 3. Patients with clinical diagnosis of Temporomandibular Joint Dysfunction Exclusion Criteria: 1. patients with clinically diagnosed acute inflammation of the outer ear, middle ear, sinuses of the nose 2. patients allergic to nimesulide or cannabidiol oil 3. patients with contraindications to include therapy with nimesulide or cannabidiol oil such as: - gastric or duodenal ulcer disease, - severe blood clotting disorders, - severe liver dysfunction, - severe renal impairment, - severe heart failure, pregnancy, - breastfeeding, - concomitant intake of citrochrome blockers CYP3A4 or CYPP2D6 (warfarin, macrolides, calcium channel blockers, benzodiazepines, cyclosporine, sildenafil, SSRI, tricyclic antidepressants, opioids)

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Cannabidiol Oil
Cannabidiol oil will be given twice a day, in a dose of 33,6mg, applied orally. The therapy will last 15 days.
Nimesulide
Nimessulid will be given twice a day - 2x100mg, applied orally. The therapy will last 15 days.

Locations

Country Name City State
Poland Chair and Depratment of Dental Prosthetics Szczecin

Sponsors (1)

Lead Sponsor Collaborator
Pomeranian Medical University Szczecin

Country where clinical trial is conducted

Poland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain relief Measured on Visual Analogue Scale (VAS) scale. It consists of a line, approximately 100mm in length, at the left end of the scale "Score 0" which means "no pain", at the right end of the scale "Score 100mm" which means "worst imaginable pain" 15 days
Primary Psychological conditions Measured on The General Health Questionnaire-28 (GHQ-28) 15 days
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