Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Glac Biotech Co., Ltd
Age
50–85
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Subjects are between 50-85 years old, and clinical diagnosis of T2DM (HbA1c ≥ 6.5% or fasting plasma glucose ≥ 126 mg/dL or oral glucose tolerance test 2-hour plasma glucose ≥ 200 mg/dL).
Patients with stable pulmonary obstruction (pulmonary function FEV1/FVC \<0.7) with symptoms of pulmonary obstruction.
Subjects can cooperate with the collection of experimental specimens and return for regular visits.
The patient or family members have signed the informed consent form.
The patient must receive adjuvant treatment with probiotic for 12 weeks.
You may not be if
The patient or caregiver is unable to follow the physician's instructions for the trial, including the completed symptom assessment form and compliance with medication.
The patient has a history of related allergic reactions, or the use of other highly sensitive or contraindicated drugs (Allergy to antibiotics or antipyretics).
The patient have taken oral immunosuppressive drugs, intravenous steroids or T cell inhibitor ointments within the past 2 weeks.
The patient has consumed probiotic-related products (including drops, lozenges, capsules, powder and yogurt) within the past 1 month.
The patient received high doses of steroids within the past 1 month.
The patient with active infection or severe pulmonary disease (eg, tuberculosis, bronchiectasis, or fibrosis).
The patient is receiving treatment for a major disease or congenital disease.
The patient is not suitable to participate in the trial as assessed by the professional physician.
