- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05980975
The Effect of Coffee and Hot Water on Gastroıntestınal Functıons
The Effect of Coffee and Hot Water Consumptıon on Gastroıntestınal System Functıons After Cesarrean Sectıon
The aim of this study is to examine the effects of coffee and hot water consumption on gastrointestinal system functions after cesarean section performed under general anesthesia. The study is in a randomized controlled experimental design.
The sample of the study consisted of 25 participants in the coffee group (Group 1), 26 participants in the hot water group (Group 2) and 27 participants in the control group (Group 3). After cesarean section, at the 4th, 8th and 12th hours of the operation, the first intervention group (coffee group) received 2 gr. granulated coffee, the second intervention group (hot water group) was given 100 ml of 50-60 C0 sugar-free hot water, the third group (control group) was given no intervention other than routine applications.
Study Overview
Status
Intervention / Treatment
Detailed Description
Objective: The aim of this study is to examine the effects of coffee and hot water consumption on gastrointestinal system functions after cesarean section performed under general anesthesia.
Materials and Methods: The study is in a randomized controlled experimental design. Patients who had an uncomplicated cesarean section under general anesthesia, were older than 18 years of age, completed the 37th week of pregnancy, did not have any gastrointestinal system disease that could affect the results of the study, and did not use drugs, and who could understand and speak Turkish were included in the study. The sample of the study consisted of 25 participants in the coffee group (Group 1), 26 participants in the hot water group (Group 2) and 27 participants in the control group (Group 3). After cesarean section, at the 4th, 8th and 12th hours of the operation, the first intervention group (coffee group) received 2 gr. granulated coffee, the second intervention group (hot water group) was given 100 ml of 50-60 C0 sugar-free hot water, the third group (control group) was given no intervention other than routine applications.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Mersin, Turkey
- Mersin University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Cesarean section performed by the physician determined in the research
- Over 18 years old,
- Completing the 37. gestational week,
- Do not have any gastrointestinal system disease that may affect the results of the research and do not use drugs,
- Able to understand and speak Turkish,
- Women who voluntarily participated in the study
Exclusion Criteria:
- Cesarean section performed by a different physician than the physician determined in the study.
- Younger than 18,
- Not completing the 37.gestational week
- Having any gastrointestinal system disease that may affect the research results and using medication
- Can't understand or speak Turkish.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Coffee group (Group 1)
Then, at the 4th hour, 8th hour and 12th hour of the surgery, the patients in the coffee group received 10 gr.
granulated coffee.
|
4th hour, 8th hour and 12th hour of after the surgery, the patients in the coffee group received 10 gr.
granulated coffee.
|
|
Experimental: Hot water group (Group 2)
The patients in the hot water group were given 200 ml of 50-60 C0 sugar-free hot water at the 4th hour, 8th hour and 12th hour of the operation.
|
hot water group were given 200 ml of 50-60 C0 sugar-free hot water at the 4th hour, 8th hour and 12th hour of after the operation
|
|
No Intervention: Control group (Group 3)
No application was made to the control group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
First bowel sound time listened with stethoscope
Time Frame: 24 hours
|
After cesarean section, the four quadrants of the abdomen were listened to every hour for the first 12 hours and every 4 hours for the next 12 hours by the investigator, and the first bowel sound time was determined by the investigator.
|
24 hours
|
|
First gas output, first defecation output, nausea and vomiting by the patient's statement checklist
Time Frame: 24 hours
|
Nausea, vomiting, first gas and first defecation times were determined by the patient's statement.
|
24 hours
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- MersinUniversityy
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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