Anesthetic Success of Inferior Alveolar Nerve Block for Mandibular Molars With Symptomatic Irreversible Pulpitis in Women Taking Selective Serotonin Reuptake Inhibitors
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Local Anesthesia
- Sponsor
- Isfahan University of Medical Sciences
- Enrollment
- 90
- Locations
- 1
- Primary Endpoint
- the success rate of the IAN block
- Status
- Completed
- Last Updated
- 7 years ago
Overview
Brief Summary
To evaluate the success of inferior alveolar nerve block (IANB) for mandibular molars with irreversible pulpitis in women under treatment with selective serotonin reuptake inhibitors (SSRIs).
Detailed Description
Seventy patients with a diagnosis of symptomatic irreversible pulpitis in one mandibular molar were assigned to either SSRI users or SSRI non-users groups. SSRIs users were 45 women who take SSRIs referred for endodontic treatment from a psychiatric clinic to the clinic of the endodontic department of Isfahan University of Medical Sciences. SSRIs non-users were 45 women who did not take SSRIs referred for endodontic treatment to the same dental clinic. The protocol of the study was approved by the Ethics Committee of the university (no. 394867). Written informed consent was obtained from all the patients. The level of anxiety of the patients was determined by using the Corah Dental Anxiety Scale. The patients registered their baseline pain severity using a Heft-Parker visual analogue scale (HP-VAS). Two standard IANBs (1.8-mL cartridges) of 2% lidocaine with 1:100,000 epinephrine (Darupakhsh, Tehran, Iran) were administered to each patient. Fifteen minutes after injection, the teeth were isolated. Access cavity preparation was started. The patients was instructed by the same operator to mark his or her pain experienced during the access cavity preparation.
Investigators
Masoud Saatchi, DDS MSc
Professor of Endodontics, School of Dentistry, Isfahan University of Medical Sciences
Isfahan University of Medical Sciences
Eligibility Criteria
Inclusion Criteria
- •vital mandibular molar tooth
- •diagnosis of symptomatic irreversible pulpitis
Exclusion Criteria
- •younger than 18 years old
- •history of significant medical conditions
- •allergies to local anesthetics or sulfites
- •pregnancy
- •active sites of pathosis in area of injection
- •inability to give informed consent
Outcomes
Primary Outcomes
the success rate of the IAN block
Time Frame: taking any type of SSRI for at least six weeks prior to the study