Pain, Postoperative
Conditions
Interventions
In this randomized, double-blind, controlled clinical trial, no premedication will be applied to patients. Preoperative data will be collected from patients, including age, sex, physical status and BM
Sponsors
Fundação São Paulo - Campus Sorocaba da Faculdade de Ciências Médicas e da Saúde da Pontifícia Universidade Católica de São Paulo
Fundação São Paulo - Campus Sorocaba da Faculdade de Ciências Médicas e da Saúde da Pontifícia Universidade Católica de São Paulo
Eligibility
Age
18 Years to 66 Years
Inclusion criteria
Inclusion criteria: Age from 18 to 66 years; patients who will be operated by Laparoscopic Cholecystectomy; American Society of Anesthesiology (ASA) physical status I or II
Exclusion criteria
Exclusion criteria: Refusal to participate in the study; inability to communicate due to changes in the level of consciousness, neurological disease or psychiatric illness; contraindication to any of the medications used in the study in question; history of alcohol or drug abuse;body mass index (BMI) greater than or equal to 40Kg/m²
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find the effectiveness of Dipyrone as a postoperative pain reducing agent, by carrying out Quality of Recovery-15 (QoR-15) questionnaires. | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary stages expected | — |
Countries
Brazil
Contacts
Public ContactEduardo Moro
Fundação São Paulo - Campus Sorocaba da Faculdade de Ciências Médicas e da Saúde da Pontifícia Universidade Católica de São Paulo
Outcome results
None listed