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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03590262
Other study ID # 723
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date January 1, 2018
Est. completion date September 30, 2019

Study information

Verified date May 2018
Source Shenzhen People's Hospital
Contact Xiuzhen Zhang
Phone 86-13714902238
Email 876538754@qq.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Aim Evidence of a possible connection between gut microbiota and several physiological processes linked to type 1 diabetes is increasing. However, the effect of multistrain probiotics in people with type 1 diabetes remains unclear. This study investigated the effect of metformin as add-on therapy on glycemic control and other diabetes-related outcomes in people with type 1 diabetes.


Description:

Design An open-label, add-on, self-control clinical trial. Setting Diabetes clinic of a teaching hospital in Shenzhen China Participants A total of 20 participants with type 1 diabetes, aged 18-60 years, will be recruited and treated with metformin as add-on therapy with insulin for 12 weeks.

Outcomes Primary outcomes were glycemic control related parameters, and secondary outcomes were anthropomorphic variables, lipid profile, blood pressure and high-sensitivity C-reactive protein. The gut microbiota profile will be analyzed before and after intervention .


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date September 30, 2019
Est. primary completion date March 31, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

type 1 diabetes patients age 18-60years old 18 Kg/m2=BMI=30Kg/m2 ketonuria (-);

Exclusion Criteria:

pregnancy lactation having other severe chronic illnesses taking other anti-diabetic drugs

Study Design


Intervention

Drug:
Metformin
take the metformin 500mg twice or three times a day

Locations

Country Name City State
China Shenzhen People's Hospital Shenzhen Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Shenzhen People's Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of hemoglobin A1c in percentage analyze the change of hemoglobin A1c before and after the treatment 3 months
Secondary Change of weight in kilograms analyze the change of weight in kilograms before and after the treatment 3 months
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