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Clinical Trials/IRCT20230210057378N1
IRCT20230210057378N1
Recruiting
Phase 3

Comparing anesthetic efficacy of 4% Articaine and 2% Lidocaine as buccal infiltration in mandibular ramus block harvesting for bone augmentation in implant patients requirin bone augmentation

Qazvin University of Medical Sciences0 sites20 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
Qazvin University of Medical Sciences
Enrollment
20
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

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

Outcomes

Primary Outcomes

Not specified

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