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 @ 1:38 AM
Ignite Modification Date:
2025-12-25 @ 1:38 AM
NCT ID:
NCT03674294
Eligibility Criteria:
Inclusion Criteria:
* Diagnosed by pathology as gastrointestinal carcinoma and no previous FOLFOX or FOLFIRI based regimen chemotherapy history.
* Female.
* Adult patients ( ≥ 18, ≤ 50 years of age)
* No long-term or excessive alcohol intake history:1.Alcohol intake less than 5 times per week; 2.Alcohol intake less than 100g per day.
* Performance status ECOG 0-1
* Adequate haematological, hepatic, renal and metabolic function parameters:
Leukocytes : 3,500-10,000/mm3, ANC ≥ 1,500/mm3, Platelets ≥ 90,000/mm3, Hb \> 9g/dl (may be transfused or treated with erythropoietin to maintain or exceed this level), Serum creatinine ≤ 1 x upper limit of normal, Bilirubin ≤ 1.5 x upper limit of normal, Serum AST, ALT, ALP ≤ 2.5 x upper limit of normal in absence of liver metastases, or ≤ 5 x upper limit of normal in presence of liver metastases.
* Negative pregnancy test. If pregnancy test were positive, subject should be included in the trial only when the subsequent pregnancy test is negative.
* Ability of reading, comprehending and finishing trial questionnaires and record, including VAS (Visual Analogue Scale) question.
* Before subject registration, written informed consent must be given according to local regulations.
Exclusion Criteria:
* Pregnant women without morning sickness.
* Presence of gastrointestinal tract obstruction or electrolyte imbalance.
* Any history of central nervous system disease(e.g. Primary brain tumour, seizure not controlled with standard medical therapy, brain metastases or history of stroke).
* Contraindication of glucocorticoid:1.Infection of virus, bacteria or fungus uncontrolled by antibiotics; 2.Active stomach or duodenum ulcer; 3.Severe hypertension, atherosclerosis, diabetes; 4.Osteoporosis;5.Corneal ulcer; 6.Pregnancy; 7.Reparative phase of trauma, operation or fraction; 8.Hypercortisolism; 9.Severe mental disorder or epilepsy; 10.Inadequate cardiac or renal function.
* Mental disability or severe emotional or mental disorder.
* Active infection(e.g. pneumonia, hepatitis) or any uncontrolled disease(e.g.diabetic ketoacidosis) that may affect study outcome or expose patients to unnecessary risk.
* Usage of any illicit drug, including medical marijuana or alcohol abusing(China drug dependence criteria).
* Treatment of unapproved medicine in the previous 4 weeks.
* Concomitant therapy of psychotropic medicine such as olanzapine.
* Hypersensitivity history towards Aprepitant, 5-HT3 receptor antagonist or dexamethasone.
* Previous treatment of Aprepitant.
* Unable to swallow capsules.
* Main researchers considered that the patient is unsuited to the trial.
* Unable or unwilling to follow research programme.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
50 Years
Study:
NCT03674294
Study Brief:
Protocol Section:
NCT03674294