Esophageal motility disorders
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients over 18 and under 65;Signed consent form; No known esophageal pathologies; Undergoing diagnostic EDA under conscious sedation
Exclusion criteria
Exclusion criteria: Under 18 or over 65 years old; Refusal to sign the consent form; previously known esophageal pathologies; Undergoing therapeutic examination; Examination performed without sedation or under general anesthesia; Need for the use of scopolamine during the performance of the diagnostic examination before the evaluation for the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find a reduction in the number of esophageal contractions after the administration of L-menthol and scopolamine. This outcome will be verified through the count of esophageal contractions that occurred during the period of one minute after the use of L-menthol or scopolamine. The digestive endoscopy will be filmed and an evaluator will perform the count. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find a smaller number of adverse effects due to the use of L-menthol compared to scopolamine. Since tachycardia is the main adverse effect of scopolamine, patients' heart rate will be measured before, during, and after the application of L-menthol or scopolamine. One of the advantages of L-menthol is believed to be its only local action. Therefore, a comparison will be made between the participants' heart rates. | — |
Countries
Brazil