Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:44 AM
Ignite Modification Date:
2025-12-25 @ 1:44 AM
NCT ID:
NCT06782594
Eligibility Criteria:
Inclusion Criteria:
1）Voluntary participation and signing of informed consent;
2\) Aged ≥18 years and ≤75 years and BMI≤28kg/m2, regardless of gender;
3\) Patients undergoing elective laparoscopic-assisted intestinal resection and the surgical site is part of the intestinal segment from the ileocecal region to the sigmoid colon;
4\) Vital organ functions meet the following requirements:iver function:
ALT and AST≤3×ULN, total bilirubin level≤2×ULN;
Renal function: serum creatinine (Cr)≤1.5×ULN or creatinine clearance≥50mL/min (when Cr\>1.5×ULN);
Blood routine examination: hemoglobin (HGB)≥80g/L;
Blood biochemistry: albumin (ALB)≥30g/L;
5\) Those classified as physical condition 1 to 3 by the American Society of Anesthesiologists (ASA).
Exclusion Criteria:
1\) Patients with a history of clinically significant drug allergy or known allergy to the study drug ingredients and excipients;
2）Those who have a history of severe heart, lung, liver, kidney, blood, endocrine, immune, skin, neurological or mental diseases in the past two years or currently have diseases of the above systems;
3\) Those with a history of drug abuse in the past 6 months;
4\) Those with a history of constipation in the past 6 months (less than 3 bowel movements per week);
5\) Severe mechanical intestinal obstruction that is not expected to be relieved after surgery, short bowel syndrome, significant gastrointestinal motility disorders (such as gastroparesis, scleroderma, chronic intestinal pseudo-obstruction), poorly controlled Those with diabetes (HbA1c\>8.5%) or gastrointestinal pacemakers installed in their bodies;
6\) Patients with inflammatory bowel disease (ulcerative colitis or Crohn's disease) and intestinal adhesions;
7\) Those who have undergone major abdominal surgery (such as gastrectomy, gastric bypass, sleeve gastrectomy, gastric band surgery, Whipple surgery, pancreatectomy, colectomy, hemicolectomy);
8\) QTcF interval: ≥450 milliseconds for men and ≥470 milliseconds for women (the QT interval must be corrected for heart rate using the Fridericia formula \[QTcF\]);
9\) Patients who received chemotherapy within 4 weeks before surgery;
10\) Those who are scheduled for emergency surgery or undergo any of the following surgeries: appendectomy, low anterior resection, colostomy, ileostomy, or stoma reversal, or diagnosed with needing proctocolectomy/low anterior resection Subjects whose disease may cause impaired rectal function or postoperative incontinence (except for lesions that do not involve the sigmoid colon and above);
11\) Within 3 days before the first dose, patients had received stimulants such as alvimopan, erythromycin, prucalopride, metoclopramide, domperidone, cisapride, mosapride, renzapride or azithromycin. Gastrointestinal motility drugs;
12\) Pregnant or lactating women, as well as those who plan to become pregnant or donate sperm or eggs during the study period and within 3 months after the end of the study, and are unwilling to use a medically recognized contraceptive measure (such as intrauterine contraceptive device or contraceptive) during the study period. sets);
13\) Participated in other clinical trials within 3 months before enrollment;
14\) Other subjects deemed unsuitable for inclusion by the researcher.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT06782594
Study Brief:
Protocol Section:
NCT06782594