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Influences of aqueous extract of M. oleifera leaves on the blood biochemical biomarkers and gut microbiota of healthy human

Influences of aqueous extract of M. oleifera leaves on the blood biochemical biomarkers and gut microbiota of healthy human

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOh-17010523
Enrollment
Unknown
Registered
2017-01-26
Start date
2017-02-19
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intesitnal function

Interventions

50mg/kg body weight aqueous extract of M. oleifera leaves:self drinking

Sponsors

College of Life Sciences, Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
22 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. Healthy young adults aged from 22-35 with good life style living in Changchun city for more than 1 year; 2. All regular check-up indicators of young adults are in the range of normal reference; 3. They did not have the experience of eating M. oleifera and its relative products.

Exclusion criteria

Exclusion criteria: 1. People have received treatment for diabetes, hypertension, or dyslipidemia, nor did they have any acute or chronic inflammatory diseases, infectious diseases, viral infections, cancer, or had a previous cardiovascular event at study entry. They had received any antibiotic therapy, prebiotics, probiotics or vitamin supplements or any other medical treatment influencing intestinal microbiota during the 3 months before and during the study (2 month before, 1month during the study); 2. Pepole who take antibiotics, catch a cold, fever, diarrhea or other physical discomfort in 3 months before and after the intervention of (1 month before intervention, 2 months during and after intervention); 3. People who have smoking, alcohol drinking, carbonic acid beverage drinking, probiotics and prebiotics supplements administration habits; 4. People who have participated in other clinical trials; 5. Other reasons are not suitable for clinical subjects, according to the researchers.

Design outcomes

Primary

MeasureTime frame
blood biochemical measurements;gut microbiota;Anthropometry parameters;

Countries

China

Contacts

Public ContactHongyu Xiang

College of Life Sciences, Jilin University

hyxiang@jlu.edu.cn+86 13944865511

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026