Comparing anesthetic efficacy of 4% Articaine and 2% Lidocaine in mandibular bone grafts
Phase 3
Recruiting
- Conditions
- Severe bone defects in the jaws.
- Registration Number
- IRCT20230210057378N1
- Lead Sponsor
- Qazvin University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
People between 18 and 65 years old
Systemically healthy people
Having the ability to fill out questionnaires
People with bone defects in the edentulous area and candidate for bone graft
People who need implants in the upper jaw or the opposite side of the bone removal area in the lower jaw (contralateral)
Exclusion Criteria
Presence of an abscess or any pathological lesion at the injection site
History of diabetes, cardiovascular diseases, hypertension and kidney diseases
History of allergy to Lidocaine or Articaine local anesthetics
Consumption of alcohol or any pain reliever
Mentally unable to give informed consent
pregnancy and breastfeeding
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Percentage of people who have pain during surgery. Timepoint: The presence of pain during surgery and throughout its duration. Method of measurement: Asking the patient about the presence or absence of pain.
- Secondary Outcome Measures
Name Time Method