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Clinical Trial Summary

Patients with orofacial pain lasting at least 3 months. The patients will be randomly assigned to one of the two groups according to the treatment method: group I (intraoral injection) and group II (transcutaneous injection) where each patient injected Botox at each trigger point according to the treatment group by the same operator. Patients will be examined by a blinded investigator at pre- and post-injections at the following intervals: during diagnosis, 1 week, 4, and 6 weeks post-injection. The patients will be assessed using a pain score measured on a 10-point visual analog scale (VAS). The secondary outcome assessed will be measuring the quality of life in an Oral Health Impact Profile questionnaire (OHIP-14).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05673655
Study type Interventional
Source Fayoum University
Contact
Status Enrolling by invitation
Phase Phase 2
Start date December 25, 2022
Completion date February 25, 2023

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