Evaluation of the effect of vitamin B supplementation on pain caused by implant surgery
Not Applicable
Recruiting
- Conditions
- Mandibular implants.Presence of tooth-root and mandibular implantsZ96.5
- Registration Number
- IRCT20180630040290N5
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 46
Inclusion Criteria
Satisfaction to participate in the study
Sensory disorder and unilateral pain in the mandible due to the implant placement
Healthy patients without the use of special drugs
Exclusion Criteria
Inability of the patient to follow the treatment and clinical examinations of the study
Previous history of inferior alveolar nerve injury
People with primary neurological problems such as neuropathies and paresthesia
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain after surgery. Timepoint: It will be done 14, 28 days and 1, 2 and 3 months after receiving treatment. Method of measurement: Visual Analogue Scale.;Postoperative malaise. Timepoint: It will be done 14, 28 days and 1, 2 and 3 months after receiving treatment. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method