The pain caused by the separator placement. Chronic intractable pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The samples are in the age range of 18-35, who can execute the study carefully and sign the consent form voluntarily The samples lack any specific systemic disease (such as gastrointestinal and coagulation diseases, etc.) The selected teeth are vital and have no endodontic problems The selected teeth have no periodontic problems The sample doesn't mention any pain in other teeth or other parts of the oral cavity The contact of the first permanent molar with its adjacent teeth is tight so that the banding of the first permanent molar in the beginning of the treatment requires two-way separating ( is checked using dental floss) Lack of space in the desired jaw There is a tooth in front of first permanent molar in front jaw
Exclusion criteria
Exclusion criteria: Taking any medication during the study Separator loss Not completing the questionnaire Improper use of mouthwash History of allergy to Berberine Pregnancy or breastfeeding
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain scale based on Visual Analogue Scale. Timepoint: Immediately after separator placement, 2 hours later and 6 hours later on the first day, at 10 am and 6 am on the second and third days, at 10 am on the seventh day. Method of measurement: Description of the patient's pain based on the Visual Analogue Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Ahvaz University of Medical Sciences