Postoperative nausea and vomiting. Surgical follow-up care, unspecified
Conditions
Interventions
By screening the list of patients to be operated, those patients who met study inclusion criteria were determined. Those who were selected for enrollment in the study were informed about nausea occurr
and groups were evaluated for presence of any difference.
At postoperative period
Experimental Group: Within the first 12 hours after the operation, acupressure with wristband was applied to patient group. Anesthesiologists were informed of these patients group to make sure that th
Treatment - Devices
and groups were evaluated for presence of any difference.
At postoperative period
Sponsors
Tek Grup
Eligibility
Sex/Gender
Female
Age
18 Years to 64 Years
Inclusion criteria
Inclusion criteria: Age between 18-65 years, Patient underwent gynecological operation; Operation was performed under general anesthesia; The patient had no cognitive; sensory or verbal communication issues; Patient volunteered to participate in the study.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Nausea, vomiting, and comfort level at the postoperative period. Timepoint: Postoperative period. Method of measurement: This was a single-center, randomized-controlled experimental study conducted in the Turkey. | — |
Secondary
| Measure | Time frame |
|---|---|
| Nausea, vomiting, and comfort level at the postoperative period. Timepoint: Postoperative period. Method of measurement: This was a single-center, randomized-controlled experimental study conducted in the Turkey. | — |
Countries
Turkey
Contacts
Public ContactNurten Kaya
Istanbul University
Outcome results
None listed