This study aims to evaluate the efficacy of Chanyanning granules in patients undergoing endoscopic resection of colorectal polyps with a basal diameter of 5-30 mm. From one day before the procedure to five days postoperatively, patients will be administered Chanyanning granules. The study will observe intraoperative and postoperative bleeding, perforation, and digestive system-related clinical symptoms such as postoperative abdominal pain, bloating, diarrhea, constipation, hematochezia, and fatigue, as well as related inflammatory markers, to determine the therapeutic effect of Chanyanning granules.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
1,000
From one day before the procedure to five days postoperatively, patients in the experimental group will be administered Chanyanning granules.
control
Second Affiliated Hospital, School of Medicine, Zhejiang University
Hangzhou, Zhejiang, China
serum interleukin-6
Time frame: From enrollment to the end of treatment at 2 weeks
The incidence of complications
The incidence of complications (blood in stool, perforation) and postoperative discomfort symptoms (abdominal pain, abdominal distension, diarrhea, constipation, fatigue, fever, etc.) were compared between the experimental group and the control group (primary endpoints).
Time frame: From enrollment to the end of treatment at 2 weeks
white blood cells
Time frame: From enrollment to the end of treatment at 2 weeks
C-reactive protein
Time frame: From enrollment to the end of treatment at 2 weeks
erythrocyte sedimentation rate
Time frame: From enrollment to the end of treatment at 2 weeks
hospital stay
Time frame: From enrollment to the end of treatment at 2 weeks
hospitalization costs
Time frame: From enrollment to the end of treatment at 2 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.