Gastrointestinal Motility
Conditions
Keywords
coffee consumption, Cesarean section, intestinal motility
Brief summary
Randomized controlled trial in Obstetrics and Gynecology department (MULTI-CENTRIC).To measure the effect of coffee consumption on intestinal motility after caesarean section for the patient who fulfills the criteria. Then they will be randomized to 3 groups. The primary outcome and secondary outcome will be measured.
Detailed description
Randomized controlled trial. Participants who fulfill the inclusion criteria (elective caesarian section, singleton pregnancy, term, viable fetus), and exclusion criteria (medical disorders, known intestinal diseases, past history of intestinal surgery, intraoperative diagnosis of extensive adhesion, intraoperative complications e.g., intestinal injury and ureteric injury intraoperative complication that can lengthen the operation time, postoperative complications like anesthesia complication and electrolytes imbalance ) Then they will be randomized to 3 groups. Group 1, will start to drink coffee 6 hours postoperative for maximum 3 doses (100ml), 8 hours apart, diet will start after 1st audible bowel sound. Group 2, will drink water 6 hours postoperative. Diet will start after 1st audible bowel sound. Group 3 is the control group and they will be (NOTHING PER ORAL) for 24 hours on intravenous fluid (3 LITRES/24 HOURS). Diet will start after 1st audible bowel sound. Primary outcome: passage of stool. Secondary outcome: passage of flatus, audible intestinal sound time, feeding time, pain scale by Visual Analogue Scale (VAS), amount, and type of analgesia needed, breastfeeding time, mobilization and hospital stay.
Interventions
DIETARY_SUPPLEMENTcoffee
Nescafe brand of coffee made by Nestlé, red mug 100 % pure coffee 12083811
Sponsors
Armed Forces Hospitals, Southern Region, Saudi Arabia
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No
Inclusion criteria
* elective caesarian section, singleton pregnancy, term, viable fetus
Exclusion criteria
* medical disorders, known intestinal diseases, past history of intestinal surgery, intraoperative diagnosis of extensive adhesion, intraoperative complications e.g., intestinal injury and ureteric injury intraoperative complication that can lengthen the operation time, postoperative complications like anesthesia complication and electrolytes imbalance )
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| passage of stool. | 72 hours | passage of stool within 72 hours. (time to be recorded by 24-hour clock from finishing of surgery) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Audible intestinal sound time. | 72 hours | Audible first intestinal sound time.(time to be recorded by the 24-hour clock from finishing of surgery). |
| Feeding time | 72 hours | Feeding time (StARTING OF REGULAR DIET ).(time to be recorded by the 24-hour clock from finishing of surgery). |
| Pain scale by VAS (Visual Analogue Scale ). | 72 hours | Pain scale by using Visual Analogue Scale(VAS). it is measuring the distance (mm) on the 10-cm line between the no pain anchor and the patient's mark, providing a range of scores from 0-100. No pain (0-4 mm), mild pain (5-44 mm), moderate pain (45-74 mm), and severe pain (75- 100 mm). |
| Type of analgesia needed. | 72 hours | Type of analgesia needed. (paracetamol, nonsteroidal anti-inflammatory drugs or pethidine ). |
| Passage of flatus. . The amount of analgesia. The first Breastfeeding time. The initiation of Mobilization. Hospital length stay. | 72 hours | (time to be recorded by the 24-hour clock from finishing of surgery). |
| The first Breastfeeding time. | 72 hours | (time to be recorded by 24-hour clock from finishing of surgery) |
| The initiation of Mobilization. | 72 hours | (time to be recorded by 24-hour clock from finishing of surgery) |
| Hospital length stay. | 72 hours | ( in Days ) |
| The amount of analgesia . | 72 hours | ( recording of dose and frequency in time are mandatory ). |
Countries
Saudi Arabia
Contacts
Primary ContactMufareh Asiri, SBOG
Outcome results
None listed