Intestinal dysfunction after abdominal surgery
Conditions
Interventions
placebo-control group:Take 6 placebo tablets
conventional-dose group:Take 6 tablets of Bacillus Coagulans Tablets, Live
high-dose group:Take 10 tablets of Bacillus Coagulans Tablets, Live
Sponsors
Third Hospital of Shanxi Medical University, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Shanxi Tongji Hospital
Eligibility
Sex/Gender
Female
Age
16 Years to 70 Years
Inclusion criteria
Inclusion criteria: 1. Aged 16-70 years; 2. Have received laparoscopic surgery; 3. The operation time is 1-4 hours; 4. Be willing to sign informed consent.
Exclusion criteria
Exclusion criteria: 1. Suffering from cognitive impairment, Alzheimer's disease, depression, etc.; 2. Have a history of abdominal and intestinal surgery or are allergic to probiotics; 3. Intraoperative blood loss of more than 400mL; 4. Poor medication compliance, resulting in invalid results; 5. Within 3 months of participating in or completing other clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the first flatus time; | — |
Secondary
| Measure | Time frame |
|---|---|
| the first defecation time;the time to first bowel sounds;incidences of postoperative complications;the duration of hospital stay; | — |
Countries
China
Contacts
Public ContactChen Weihong
Outcome results
None listed