Viewing Study NCT02660593


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Study NCT ID: NCT02660593
Status: UNKNOWN
Last Update Posted: 2016-04-27
First Post: 2016-01-17
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Efficacy and Safety ofSanGrow Decoction for Patients With Diabetes
Sponsor: Shidaihuajing Institute for Diabetic Research
Organization:

Study Overview

Official Title: SanGrow Decoction in Patients With Diabetes- Single Center, Open, and Non-randomized Study
Status: UNKNOWN
Status Verified Date: 2016-01
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: MedlinePlus related topics: Blood Sugar

Primary Outcome Measures:

* Fast glucose and HbA1c change between the baseline and end of study \[ Time Frame: From baseline to 30 and 100 days\]
* \[ Designated as safety issue: No \]
* Successful rate of blood glucose control (the proportion of patients with HbA1c \<7%) \[ Time Frame: From baseline to 30 days and 100 days\] \[ Designated as safety issue: No \]

Secondary Outcome Measures:

• To evaluate the change of quality of life in the 1 months by the health questionnaire SF-36 \[ Time Frame: From baseline to month 1 \] \[ Designated as safety issue: No \]
Detailed Description: This study is aimed to evaluate the safety and efficacy of Sangrow Decotion, diet and exercise for the treatment of type 2 diabetes. Previous study has shown that this therapeutic regimen is safe and effective.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: