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Comparison of pain levels in nasopalatine nerve blocks using two different techniques

Comparison of pain levels in nasopalatine nerve blocks using two different techniques

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9h2kdm9
Enrollment
Unknown
Registered
2022-08-15
Start date
2014-06-01
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 Caries

Interventions

This is a crossover, double-blind, randomized clinical trial involving 32 participants. A researcher (researcher #1), with no direct participation in the procedures performance or pain assessments, ra

Sponsors

Universidade Federal de Sergipe
Lead Sponsor
Universidade Federal de Sergipe
Collaborator

Eligibility

Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: Both genders; age between 18 and 30 years; any ethnicity; any marital status; any nationality; any place of birth; with previous experience of local anesthesia without intercurrences; not having undergone infiltrative anesthesia in the region in the two weeks prior to the study; and not having used any medication capable of altering pain perception in the two weeks prior to the study

Exclusion criteria

Exclusion criteria: Age lower than 18 years or higher than 30 years old; pregnant or lactating women; history of hypersensitivity to the drugs used in the study; alcohol abuse or drug dependence; psychiatric disorders or systemic diseases; being under treatment with CNS-acting drugs; use of drugs capable of altering pain perception in the two weeks preceding the study; and moderate anxiety or higher (over 9), based on Corah's Dental Anxiety Scale

Design outcomes

Primary

MeasureTime frame
Expected outcome: It is expected to find lower levels of pain during nasopalatine nerve block with the Morpheus® device during puncture, needle insertion and anesthetic deposition, verified by means of the Visual Analog Scale immediately after the anesthetic injection;Obtained outcome: It was observed statistically lower pain levels during nasopalatine nerve block with the Morpheus® device during the puncture, needle introduction, and local anesthetic deposition, verified by means of the Visual Analog Scale immediately after the anesthetic injection

Secondary

MeasureTime frame
No secondary outcomes are expected

Countries

Brazil

Contacts

Public ContactJohn Pinho

Universidade Federal de Sergipe

john.nadson@hotmail.com+55(79)999103008

Outcome results

None listed

Source: REBEC (via WHO ICTRP)