Clinical Trials Directory

Trials / Completed

CompletedNCT02794922

Effectiveness of Vitamin B in Reducing Temporomandibular Joint Disorder Pain

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
27 (actual)
Sponsor
The University of Hong Kong · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine effectiveness of vitamin B in reducing temporomandibular joint disorder (TMD) pain. Patients will be randomised to receive the study drug or placebo. The study drug we are using is a combination of vitamin B1(thiamine mononitrate)-242.5mg; vitamin B6(pyridoxineHCl)-250mg, and vitamin B12(cyanocobalamin)-1mg. We will assess patient's pain level, range of jaw movement and record any side effects from using this medication.

Detailed description

Type of study : Prospective double blinded randomized control trial Sample population : patients with temporomandibular joint disorder pain who are currently undergoing treatment in Oral \& Maxillofacial surgery unit, Prince Philip Dental Hospital Study Period : 2 year (1st may2015 to 1st may 2017) Data Collection All new cases or existing TMD patients treated in oral maxillofacial surgery department, Prince Philip Dental Hospital will be acquired and screened based on inclusion and exclusion criteria. Selected patients will be categorised based on TMD axis 1 diagnosis and divided into two groups - group 1(Vitamin B) and group 2(placebo) randomly . Allocation of patients into the group will be based on computer generated by random block sequence. Complete social demographic background of the patient will recorded according to the following format age, gender, race, education, and job. Clinical assessment will be done to check 1. Mouth opening 2. Lateral excursion (right and left) 3. Protrusion 4. Deviation of lower jaw on opening 5. Tenderness of muscle of mastication 6. Pain - based on 10cm visual analog score. After initial assessments, patients will be started on either vitamin B complex or placebo based on their group. * Both group of patients will be also prescribed with Tab Ibuprofen 400mg to be taken during acute Temporomandibular joint (TMJ) pain symptoms. * These patients will be reviewed on week 0,2,4 and 6. * All the patients will be reviewed by blinded assessor. Each patient will be given a log book to document frequency of TMJ pain attack, maximum pain score on each attack and amount of analgesics (Ibuprofen 400mg tabs) taken. * Log book record will be checked on their review. * Amount of analgesics recorded in log book and compliance of Vitamin B or placebo will be cross checked with remaining tablet count. Data Evaluation/ Statistical Analyses The statistical analysis of this study will use the standard version of Statistical Package for the Social Sciences (SPSS) version 17.0 for windows. All the data will be gathered and entered in into this software.

Conditions

Interventions

TypeNameDescription
DRUGNeurovit Forte
DRUGCorn Starch

Timeline

Start date
2015-09-01
Primary completion
2016-06-01
Completion
2017-07-01
First posted
2016-06-09
Last updated
2018-05-04

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02794922. Inclusion in this directory is not an endorsement.