The Prevention And Treatment On Obesity And Weight Management By Oral Supplementation Of Probiotics And Prebiotics

Sponsor
Shenzhen Precision Health Food Technology Co. Ltd., (Other)
Overall Status
Recruiting
CT.gov ID
NCT06030999
Collaborator
(none)
150
2
3
2.7
75
28.2

Study Details

Study Description

Brief Summary

The goal of this interventional study is to test whether consumption of Wonderlab probiotics with prebiotics could improve obesity and overweight in Chinese people who are aged 25-45 and overweight. The main question it aims to answer is:

  • whether the weight of participants can be lost after 10 weeks' intervention

150 participants will be randomized into 3 study groups (50 each group) in the two study sites, who will consume assigned product according to instructions for 10 weeks. Three site visits will be made for each participant and all relevant clinical data will be captured and recorded into CTMS(Clinical Trial Management System) for statistical analysis.

Researchers will compare the three groups to conclude whether the Wonderlab study product can improve obesity and overweight over placebo product.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Study product A (Wonderlab wonder4shape)
  • Dietary Supplement: Study product B (Wonderlab wonder4shape)
  • Dietary Supplement: Study product C (placebo)
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Supportive Care
Official Title:
Three Arms, Randomized, Double-blind Controlled Trial Of Prevention And Treatment On Obesity And Weight Management By Oral Supplementation Of Probiotics And Prebiotics
Anticipated Study Start Date :
Sep 25, 2023
Anticipated Primary Completion Date :
Dec 2, 2023
Anticipated Study Completion Date :
Dec 15, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Study product A (Wonderlab wonder4shape)

2g/bottle, containing the following probiotics total dosage 2.0*1010 CFU: CECT7527, CECT7528, CECT7529 Maltodextrin Lactobacillus acidophilus Fructose oligosaccharides Grapefruit, Lemon and Apple powder

Dietary Supplement: Study product A (Wonderlab wonder4shape)
Participants in this arm need to consume one bottle (2g) of this product once a day for 10 weeks

Active Comparator: Study product B (Wonderlab wonder4shape)

2g/bottle, containing the following probiotics total dosage 1.0*1010 CFU: Maltodextrin Lactobacillus acidophilus

Dietary Supplement: Study product B (Wonderlab wonder4shape)
Participants in this arm need to consume one bottle (2g) of this product once a day for 10 weeks

Placebo Comparator: Study product C (placebo)

2g/bottle, containing the following ingredients: Maltodextrin Grapefruit powder Lemon powder

Dietary Supplement: Study product C (placebo)
Participants in this arm need to consume one bottle (2g) of this product once a day for 10 weeks

Outcome Measures

Primary Outcome Measures

  1. Change of Weight [baseline day 0, day 70]

    Change of Weight in Kg by Inbody S10 from baseline to 10 weeks

Secondary Outcome Measures

  1. Blood lipids - Total Cholesterol Level [baseline day 0, day 35, day 70]

    Blood lipids - Total Cholesterol level of blood test in mmol/L and range of 0.56-17mmol/L for each visit interval

  2. Blood Sugar Level [baseline day 0, day 35, day 70]

    Blood sugar level of blood test in mmol/L and range of 3.9-6.1mmol/L

  3. Blood hormone - Leptin level [baseline day 0, day 35, day 70]

    Blood hormone - Leptin level of blood test in ng/mL and range 0.5-15.2ng/mL

  4. Blood hormone - Adiponectin level [baseline day 0, day 35, day 70]

    Blood hormone - Adiponectin level of blood test in ug/mL and range of 2-37ug/mL

  5. Blood inflammation [baseline day 0, day 35, day 70]

    Blood inflammation (Zonulin, ApoB-48, hsCRP, LPS, sCD14, IL-6, MCP-1, Angptl4)

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years to 45 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Chinese males or females, age between 25-45;

  • Overweight population: BMI 24-27.9 & obesity population: BMI >=28;

  • Blood lipids in high potential risks but without medication:TG > 5mol/L or LDL >= 3.4 mmol/L or TC >= 5.2 mmol/L.

  • Understand the test procedure, read, and sign an appropriate Informed Consent Form indicating their willingness to participate;

  • Agree to avoid medication treatment for weight management, including blood lipids and sugar control.

Exclusion Criteria:
  • Have used any medication for weight management at least one month before this study.

  • Subject having done plastic surgery for weight management.

  • Be involved in any aspect of test administration, i.e., evaluating or overseeing activities related to product.

  • Have participated in any clinical study involving the test sites within the previous 6 months, or is subject participating in any clinical study concurrently.

  • Have a history of any type of metabolic syndrome, including but not limited to any type of diabetes, obesity and heart disease.

  • Have a history of any disease or the presence of health condition on the study sites that the Investigator feels would interfere with the study.

  • Be taking antihistamines (> 3x/week) or anti-inflammatory (> 8x/week) on a regular basis, or has the subject taken systemic or topical steroidal medications within 4 weeks of study enrolment.

  • Have any of the following conditions or factors that the investigator believes may affect the response of the skin or the interpretation of the test results, including, but not limited to, pregnancy, lactation and hepatitis.

  • Have any cuts/abrasions on the test site at baseline.

  • The subject is an employee of sponsor or the site conducting the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 SPRIM Central Lab Shanghai Shanghai China
2 Ligang Hospital Jinhua Zhejiang China

Sponsors and Collaborators

  • Shenzhen Precision Health Food Technology Co. Ltd.,

Investigators

  • Principal Investigator: Hongwei Guo, MD, Shanghai Fudan University, School of Public Health
  • Principal Investigator: Weixing Wang, MD, Shanghai Jiao Tong University School of Medicine

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Shenzhen Precision Health Food Technology Co. Ltd.,
ClinicalTrials.gov Identifier:
NCT06030999
Other Study ID Numbers:
  • 23-SM-08-WL-001
First Posted:
Sep 11, 2023
Last Update Posted:
Sep 11, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Shenzhen Precision Health Food Technology Co. Ltd.,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 11, 2023