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fenugreek extract effect on pain relief

Phase 3
Recruiting
Conditions
Temporomandibular disorders.
Temporomandibular joint disorder, unspecified
M26.60
Registration Number
IRCT20181218042039N1
Lead Sponsor
Kerman University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

Men and women over 14 years of age
Patients who be able to respond to the mentioned forms
Patients wishing to enter the study

Exclusion Criteria

Pregnancy and lactation in women
Patients with Diabetes Mellitus
patients who take statin drugs
Sensitivity to Fenugreek or other herbs
Patients with history of coagulation disorders
Patients undergoing orthodontic or orthopedic procedures
Patients treated with anti psychotropic, anti-inflammatory and analgesic drugs and splint therapy
Patients with dental caries that imitate pain in the head and face
Patients with periodontal problems
Patients with pathologic problems in the head and face

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Reduce pain in Visual Analogue Scale and Brief Pain Inventory questionnaire. Timepoint: at beginning of the study and after 14th , 28th days of the beginning of the study. Method of measurement: Visual Analogue Scale and Brief Pain Inventory of pain questionnaire.
Secondary Outcome Measures
NameTimeMethod
GI upset. Timepoint: Two and four weeks after drug administration. Method of measurement: Patient claim and Questionnaire fullfilment.
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