Hot Compress Application in Open Abdominal Surgery
Recruiting
N/A
Interventional Study
Abdominal Surgery by Laparotomy
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 – 65
- Sex
- Any
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 80 (estimated)
- Sponsor
- TC Erciyes University · Other
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About This Trial
This study aims to evaluate the effect of hot compress application to the intestines during abdominal surgery on postoperative nausea-vomiting and bowel function.
Volunteers will be randomly assigned to the intervention and control groups. Initially, 30 patients will be included in each group, and the study will be completed based on the effect size determined by power analysis.
Hypotheses:
H0:…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Abdominal surgery in the general surgery ward
* 18 years of age or older
* Patients with BMI in the normal range (18.50-24.99 kg/m2)
* Able to communicate verbally
* Those who volunteered to participate in the study
* Patients with no mental confusion, conscious and oriented w…
Contacts