Intestinal Flora and Immunity in Monoclonal Gammopathy Patients
NCT ID: NCT06539832
Last Updated: 2024-09-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
300 participants
OBSERVATIONAL
2024-05-01
2026-12-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
RETROSPECTIVE
Study Groups
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Monoclonal gammopathy patients without concurrent infection
(I) Inclusion criteria:
1. Age 45 years or older;
2. Patients screened positive for monoclonal protein by MALDI-TOF MS;
3. No symptoms of infection, with normal infection indicators (whole blood hs-CRP, serum IL-6, PCT);
4. Adequate remaining whole blood, plasma and stool samples available, and relevant case data can be provided.
(II) Exclusion criteria:
1. History of intestinal tumors, irritable bowel syndrome or inflammatory bowel disease, or diagnosed during hospitalization;
2. Received antibiotic treatment in the past one month;
3. Insufficient sample volume, or presence of severe hemolysis, lipemia, jaundice or other unqualified sample conditions.
No interventions assigned to this group
Monoclonal gammopathy patients with concurrent infection
(I) Inclusion criteria:
1. Age 45 years or older;
2. Patients screened positive for monoclonal protein by MALDI-TOF MS;
3. Presence of infection symptoms, with abnormal infection indicators (whole blood hs-CRP, serum IL-6, PCT);
4. Adequate remaining whole blood, plasma and stool samples available, and relevant case data can be provided.
(II) Exclusion criteria:
1. History of intestinal tumors, irritable bowel syndrome or inflammatory bowel disease, or diagnosed during hospitalization;
2. Received antibiotic treatment in the past one month;
3. Insufficient sample volume, or presence of severe hemolysis, lipemia, jaundice or other unqualified sample conditions.
No interventions assigned to this group
Healthy control group
(I) Inclusion criteria:
1. Age 45 years or older;
2. Patients screened negative for monoclonal protein by MALDI-TOF MS;
3. No symptoms of infection, with normal infection indicators (whole blood hs-CRP, serum IL-6, PCT);
4. Adequate remaining whole blood, plasma and stool samples available, and relevant case data can be provided.
(II) Exclusion criteria:
1. History of intestinal tumors, irritable bowel syndrome or inflammatory bowel disease, or diagnosed during hospitalization;
2. Received antibiotic treatment in the past one month;
3. Severe systemic diseases including malignant tumors;
4. Insufficient sample volume, or presence of severe hemolysis, lipemia, jaundice or other unqualified sample conditions.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2. Patients who were monoclonal gammaglobulin negative by MALDI-TOF MS screening;
3. No symptoms of infection and normal indicators of infection (whole blood hs-CRP, serum IL-6, PCT);
4. Sufficient remaining whole blood, plasma and faecal samples are available, and relevant case information can be provided.
Exclusion Criteria
2. Patients receiving antibiotic therapy in the last month
3. Severe systemic diseases including malignant tumours;
4. Insufficient remaining sample volume, or the presence of sample failure such as severe haemolysis, lipaemia or jaundice.
45 Years
ALL
Yes
Sponsors
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Zhujiang Hospital
OTHER
Responsible Party
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Principal Investigators
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Hongwei Zhou, Professor
Role: STUDY_CHAIR
Southern Medical University, China
Locations
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Zhujiang Hospital of Southern Medical University
Guanzhou, Guangdong, China
Countries
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Central Contacts
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Hongwei Zhou, Professor
Role: CONTACT
Facility Contacts
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Other Identifiers
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ZhujiangMGUS
Identifier Type: -
Identifier Source: org_study_id
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