Sleeve gasterectomy surgery.
Conditions
Interventions
Intervention group: _In the present study, in addition to the routine nursing care provided to all patients, the researcher will conduct a specialized visit for the intervention group. This visit incl
Sponsors
Karaj University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Patients between 18 and 60 years old Patients with a body mass index (BMI) = (35) kg/m2 Patients undergoing sleeve gasterectomy as a primary obesity procedure Patients who provided written informed consent to participate in the study Patients who are willing and able to complete the study steps and follow-up visits Patients undergoing surgery with a surgeon and surgical team Patients under anesthesia with an anesthesia method and anesthetic drugs Patients under care in recovery with a specific medication regimen The patient does not have active peptic ulcer disease or severe gastroesophageal reflux disease (GERD). The patient is not taking any specific medication. The patient should not have any specific underlying physical or psychiatric diseases.
Exclusion criteria
Exclusion criteria: Patients who are unable or unwilling to attend preoperative visits and follow-up assessments Failure to cooperate in completing the vomiting questionnaire A problem or unexpected event occurs during the operation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative vomiting. Timepoint: Completion of the vomiting questionnaire (Rhodse) at specified time intervals (after regaining consciousness up to 24 hours after surgery, 24-48 hours after surgery, 48-72 hours after surgery, 72 hours to 1 week, 1 week to 1 month, 1-2 months, and 2-3 months). Method of measurement: Rhodse Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFateme Soltan
Karaj University of Medical Sciences
Outcome results
None listed