- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07570329
Human Milk Oligosaccharides, Gut Bifidobacterium, Vitamin D, and Infant Immunity (HMO-BIFIDI)
Human Milk Oligosaccharides in Breast Milk and Its Relation to Gut Bifidobacterium, Vitamin D and Immune Modulation in Infants
The goal of this observational study is to learn how certain natural sugar components in breast milk may be linked with vitamin D level, healthy gut bacteria, and immune markers in healthy breastfed infants. The study will include exclusively breastfeeding mothers and their healthy infants aged 1 to 2 months.
The main questions it aims to answer are:
- Is this natural sugar in breast milk linked with the baby's vitamin D level?
- Is this natural sugar in breast milk linked with healthy gut bacteria?
- Is this baby's vitamin D level linked with healthy gut bacteria?
- Is this natural sugar linked with immune factors in breast milk? Participants will answer health questions from questionnaire, undergo a brief physical examination, allow breast milk and a small baby blood sample to be collected, and provide an baby stool sample.
Researchers will test these samples in the laboratory and analyze the results to answer the research questions.
연구 개요
상태
정황
상세 설명
Subject recruitment was conducted during immunization activities at community health centers (Puskesmas) and integrated health posts (Posyandu). The subject collection technique used the quota sampling method, a non-probability subject selection technique carried out by determining the desired sample size (quota) from a population with predetermined criteria, and researchers collected sample units until the target quota was reached. Researchers provided an explanation of the research protocol and obtained informed consent from participants regarding their willingness to participate in the study. Participants who met the eligibility criteria (inclusion and exclusion criteria) were declared as research subjects. Next, a research questionnaire was completed, including recording the subject's identity (mother and baby), the mother's health and nutritional history, childbirth and breastfeeding history, observation of the baby's stool, history and risk factors for allergies, and a general physical examination.
Mature breast milk samples will be analyzed to determine maternal secretion status, HMO status, Bifidobacterium in breast milk, and the status of immune markers such as sCD14, TGF-beta, and IgA in breast milk. Stool samples will be analyzed to determine the infant's intestinal Bifidobacterium. Blood samples will also be analyzed to determine vitamin D levels. Statistical correlations between these parameters will be performed to determine the research objectives.
The collected data is grouped based on the purpose and type of data, then the appropriate statistical method is selected, namely:
- Univariate analysis (Used to describe basic data characteristics, in the form of frequency, mean value, standard deviation, and range)
Bivariate analysis
Comparison Test (To see differences between groups)
- Chi-Square Test → If the variable is categorical (e.g., the relationship between maternal secretory status (Secretory vs. Non-Secretory) and delivery method (Vaginal vs. Cesarean section). An alternative test, the Fisher's Exact test, is performed if the basic assumptions of the Chi-Square are not met.
- T-Test (Independent T-Test) → If you want to compare the means of two groups (e.g., the difference in vitamin D levels between male and female infants). An alternative test, the Mann-Whitney test, is used if the data is not normally distributed.
- ANOVA Test → If you want to compare the means of more than two groups (e.g., the difference in vitamin D levels based on the timing of early breastfeeding initiation: <1 hour, 1-6 hours, >6 hours). An alternative test, the Kruskal-Wallis test, is used if the data is not normally distributed.
Correlation Analysis (To see the relationship between two numeric variables)
- Pearson Correlation → If the data is normally distributed.
- Spearman Correlation → If the data is not normally distributed or is ordinal
연구 유형
등록 (실제)
연락처 및 위치
연구 장소
-
-
South Sulawesi
-
Makassar, South Sulawesi, 인도네시아, 90245
- Hasanuddin University
-
-
참여기준
자격 기준
공부할 수 있는 나이
- 어린이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
샘플링 방법
연구 인구
설명
Inclusion Criteria:
Maternal Subject :
- Women aged at least 18 years who are physically healthy;
- Have a healthy baby aged 1-2 months with a full-term gestational age (37-42 weeks) and a normal birth weight (2500-4000 grams);
- Exclusively breastfeeding;
- Agree to participate in this study by signing an informed consent form.
Infant Subjects :
- All infants of mothers who meet the inclusion criteria
Exclusion Criteria:
Maternal Subject :
- Currently participating in another clinical trial;
- Having a condition such as a breast abscess or other breast pathology;
- Currently taking medications for conditions that may affect breast milk, such as antibiotics;
- Subjects who cannot comply with the study protocol
Infant Subjects:
- Currently participating in another clinical trial;
- Having a history of antimicrobial treatment (oral or parenteral antibiotics);
- Subjects are unable to comply with the research protocol.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Analysis maternal Human Milk Oligosaccharides (HMO) and Breast Milk (BM) Bifidobacterium and their correlation to gut Bifidobacterium, serum vitamin D and immune regulatory status in infants
기간: At enrollment (single time point, cross-sectional assessment)
|
This outcome analyze the correlation between maternal human milk oligosaccharide (secretor status, 2FL' level), Breast Milk (BM) Bifidobacterium, gut Bifidobacterium, serum vitamin D and immune regulatory status in infants in infants aged 1 to 2 months.
|
At enrollment (single time point, cross-sectional assessment)
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Association between maternal HMO and infant gut Bifidobacterium
기간: At enrollment (single time point, cross-sectional assessment)
|
Association between maternal human milk oligosaccharide (secretor status and 2FL' level) and Bifidobacterium abundance in infant stool.
|
At enrollment (single time point, cross-sectional assessment)
|
|
Association between maternal HMO and infant vitamin D level
기간: At enrollment (single time point, cross-sectional assessment)
|
Association between maternal human milk oligosaccharide (secretor status and 2FL' level) and vitamin D level in infant serum.
|
At enrollment (single time point, cross-sectional assessment)
|
|
Association between maternal HMO and breast milk immune markers
기간: At enrollment (single time point, cross-sectional assessment)
|
This outcome assesses the association between human milk oligosaccharide (HMO) (secretor status and 2FL' level) in breast milk and immune markers in breast milk, including soluble CD14 (sCD14), transforming growth factor beta (TGF-beta), and immunoglobulin A (IgA).
|
At enrollment (single time point, cross-sectional assessment)
|
|
Association between breast milk Bifidobacterium and infant gut microbiota
기간: At enrollment (single time point, cross-sectional assessment)
|
This outcome assesses the association between Bifidobacterium composition in breast milk and gut microbiota (Bifidobacterium) composition in infant stool samples.
|
At enrollment (single time point, cross-sectional assessment)
|
|
Association between breast milk Bifidobacterium and infant vitamin D level
기간: At enrollment (single time point, cross-sectional assessment)
|
This outcome assesses the association between Bifidobacterium composition in breast milk and vitamin D level in infant serum.
|
At enrollment (single time point, cross-sectional assessment)
|
|
Association between breast milk Bifidobacterium and breast milk immune marker
기간: At enrollment (single time point, cross-sectional assessment)
|
This outcome assesses the association between Bifidobacterium composition in breast milk and immune markers in breast milk, including soluble CD14 (sCD14), transforming growth factor beta (TGF-beta), and immunoglobulin A (IgA).
|
At enrollment (single time point, cross-sectional assessment)
|
공동 작업자 및 조사자
협력자
수사관
- 수석 연구원: Bahrul Fikri, MD, Ph.D, Department of Pediatrics, Faculty of Medicine, Hasanuddin University
- 연구 책임자: Andi Raisyiah Akrimah Imran, MD, MHA, Department of Public Health and Family Medicine, Faculty of Medicine, Hasanuddin University
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (실제)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
IPD 계획 설명
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .