Skip to content

Comparison of a local anesthetic technique applied by syringe or by computer

Comparative study of length and duration of Inferior Alveolar Nerve Block with Lidocaine 2% + Epinephrine 1: 100.000 applied by conventional technique or computerized system

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
REBEC
Registry ID
RBR-4zzc3p
Enrollment
Unknown
Registered
2018-05-23
Start date
2017-11-08
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental carie

Interventions

After selecting the sample (n=32), the volunteers will be scheduled to begin the restorative treatment. The data collected will correspond to execution time, latency and duration of anesthesia as well
Procedure/surgery
E03.155.086.231
E06.323.428

Sponsors

Universidade Federal de Sergipe
Lead Sponsor
Universidade Federal de Sergipe
Collaborator

Eligibility

Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Volunteers aged between 18 and 35 years; who have not undergone blockade anesthesia in the region in the two weeks prior to the study; present 02 lower molars in need of restorative treatment; not having used any medication that could alter the perception of pain in the two weeks prior to the study.

Exclusion criteria

Exclusion criteria: Hypersensitivity to drugs used in the study - 2% Lidocaine with epinephrine 1: 100,000; Benzocaine 20%; presence of organ dysfunction or clinically significant deviation from normal, assessed during anamnesis; odontophobic; pregnant and / or lactating women; history of drug addiction or alcohol abuse.

Design outcomes

Primary

MeasureTime frame
Increased duration of anesthetic effect through the computerized system around 40%

Secondary

MeasureTime frame
Secondary outcomes are not expected

Countries

Brazil

Contacts

Public ContactLiane Souza

Universidade Federal de Sergipe

odontoliu@gmail.com+55-079-999777001

Outcome results

None listed

Source: REBEC (via WHO ICTRP)