Pain Postoperative
Conditions
Interventions
This is a two-arm, double-blind, randomized controlled clinical trial. A total of 10 individuals who meet the eligibility criteria will then be probabilistically allocated to one or the other interven
E03.091
Sponsors
Ronainy Francieli Silva Matos
Ronainy Francieli Silva Matos
Eligibility
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Patients aged between 18 and 65 years; of both sexes; physical status ASA -I or II; undergoing Sleeve Gastroplasty will be studied
Exclusion criteria
Exclusion criteria: Patients with severe comorbidity (American Society of Anesthesiologists (ASA) physical status III or IV); cardiac arrhythmias; dilated cardiomyopathy; cardiac conduction disorder; electrolyte disorder; acid-base disorder; hypersensitivity to morphine and/or clonidine; psychiatric; hepatic; respiratory or oncological diseases; who are receiving any type of analgesic in the week prior to surgery and those who receive blood products during the study period will be excluded from the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare aspects related to the use of isolated morphine solution and morphine associated with clonidine in pain control, as well as possible adverse effects presented after administration of the agents studied, recording the type, occurrence and intensity of the events. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to evaluate patient satisfaction, considering the attention given to their needs, waiting time to obtain analgesia, information, privacy, pain control and discomfort. Such variables will be grouped into closed responses described as: not at all satisfied, somewhat satisfied, satisfied, very satisfied and completely satisfied. | — |
Countries
Brazil
Contacts
Public ContactRonainy Matos
Hospital São Domingos
Outcome results
None listed