Transcutaneous Electrical Nerve Stimulator to Improve Blood Glucose Control in Patients With Type 2 Diabetes Mellitus

Type 2 Diabetes Mellitus Clinical Trial

Official title:

A Prospective, Double Blind, Randomized, Placebo- Controlled Trial of Transcutaneous Electrical Nerve Stimulator (DW1330) to Improve Blood Glucose Control in Patients With Type 2 Diabetes

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03102424
• Other study ID #: TRWRDM1604001
• Secondary ID: 1056030994
• Status: Completed
• Phase: N/A
• Start date: April 10, 2017
• Est. completion date: July 31, 2020

Study information

• Verified date: March 2021
• Source: Taiwan Resonant Waves Research Corporation
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The primary study objective is to demonstrate the use of "Dragon Waves Resonant Home Care" Electronic Nerve Stimulator (DW1330) is associated with improvement of blood glucose control, as measured by change of glycated hemoglobin (HbA1c). The second study objectives are to demonstrate that DW1330 is associated with the mechanism of glycemic control and inflammation pathways. The study is also aimed to investigate the safety of DW1330.

Description:

This is a multi-center, prospective, double blind, randomized, placebo-controlled trial of transcutaneous electrical nerve stimulator (DW1330) to improve blood glucose control in patients with type 2 diabetes. Subjects with type 2 diabetes who meet inclusion/exclusion criteria will be randomized to either of the 2 groups below:

1. DW1330

2. Placebo (sham TENS delivering ineffective pulse wave)

After enrollment, subjects will be randomly assigned to receive one of the study treatments in a double-blind fashion. All patients enrolled should perform 1 treatment within 1 hour after dinner 5 days a week. The end of a 20 week treatment period, subjects will be followed for an additional 2 weeks for safety follow-up. The time frame includes 2 weeks of screening, 20 weeks of treatment, and 2 weeks of post-treatment follow-up.

Study visits will occur every 2 or 4 weeks depending on the study phase. At randomization visit study device will be dispensed at the site, during the treatment period visits, all Adverse Events (AEs) as well as follow-up for all AEs that have not been resolved will be recorded, changes to concomitant medications will be noted, vital signs will be taken, and efficacy evaluations will be performed as well. Investigators, site staff, subjects, and the study team will be blinded to the device assigned. The study includes collection of blood and urine samples. The end-of-treatment visit and the last estimation of glycemic control will occur at week 20 (visit 8) for all subjects. In addition, 2-week follow up will occur in order to collect safety data after the device is returned. The final visit will be at week 22 (visit 9). Subjects will be encouraged to complete all planned visits regardless of their adherence to study device administration.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 160
• Est. completion date: July 31, 2020
• Est. primary completion date: July 15, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 30 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Male and female subjects age 30 through 80 years;

2. Type 2 diabetes mellitus (T2DM) patients on stable oral anti-diabetic drugs for more than 3 months, and can maintain stable during study maintenance period;

3. HbA1c between 7.5 and 10% inclusive;

4. Subjects who are able and willing to perform self-monitoring of plasma glucose and self-administration of study device for the entire trial period;

5. Subjects who are able and willing to keep a diary;

6. Able and willing to sign informed consent and return for follow-up assessments.

Exclusion Criteria:

1. Subject has had any of the following new diagnoses within 1 year of screening:

myocardial infarction, coronary artery bypass surgery, coronary artery stenting, transient ischemic attack, cerebrovascular accident, angina, congestive heart failure(NYHA III-IV), ventricular rhythm disturbances or thromboembolic disease;

2. Subjects with prior pancreatitis;

3. Subjects with insulin therapy (except for short term uses no longer than 7 days) or injectable antihyperglycemic agents (AHAs) within 3 months;

4. Female with a positive pregnancy test, planning to become pregnant during screening, active treatment, or the follow up period, breastfeeding, or judged to be using inadequate contraceptive methods;

5. Subjects who underwent previous intra abdominal, GI tract surgery or a major abdominal trauma within 6 months prior to screening visit;

6. Subjects with other implanted electrical stimulation devices;

7. Subject has any unresolved adverse skin condition in the area of device placement;

8. ALT/AST greater than 3 x upper limit of the institution's normal range (ULN) and/or total bilirubin = 2.0 x ULN, active liver disease (other than nonalcoholic hepatic steatosis), including chronic active hepatitis B or C, hepatic cirrhosis, primary biliary cirrhosis, or active symptomatic gallbladder disease;

9. Subjects with moderate or severe renal impairment (serum creatinine =1.5 mg/dL in males or = 1.4 mg/dL in females or urine microalbumin-creatinine ratio (ACR) >300 mg/g), conditions of congenital renal glucosuria, unstable or rapid progressing renal disease;

10. Has blood dyscrasias or any disorders causing hemolysis or unstable red blood cells or any other clinically significant hematological disorder (such as aplastic anemia, myeloproliferative or myelodysplastic syndromes, thrombocytopenia, coagulopathy);

11. Subjects with acute metabolic complications (such as ketoacidosis, lactic acidosis or hyperosmolar), proliferative diabetic retinopathy or macular edema within 6 months before screening;

12. Subjects with a history of malignancy =5 years prior to screening, except for adequately treated basal or squamous cell skin cancer or in situ cervical cancer;

13. Subjects a history of alcohol or drug abuse within 1 year prior to screening;

14. Subjects who received another investigational agent within 30 days prior to screening;

15. Subjects who are unlikely to be available for follow-up as specified in the protocol;

16. Subjects with a past or present psychiatric condition that may impair his or her ability to comply with the study procedures;

17. Subjects with conditions that, in the judgment of the investigator, precludes successful participation to the study;

18. Subjects with fever(body temperature> 37.5°C), perceptual function lost, or any metal implants.

Related Conditions & MeSH terms

• Diabetes Mellitus
• Diabetes Mellitus, Type 2
• Type 2 Diabetes Mellitus

Intervention

Device:
• Transcutaneous Electrical Nerve Stimulator (DW1330)
The 20 weeks of treatment of the DW1330 device, all the patients enrolled should perform 1 treatment within 1 hour after dinner 5 days a week.
• Sham DW1330 device
The Sham DW1330 device will be masked by the same appearance as the study device (DW1330). The usage of time and location of Sham DW1330 device will be completely the same with study device (DW1330). However, the electronic model, including the frequency and time consistence of electronic stimulation are different between the Sham DW1330 device and the study device (DW1330). The 20 weeks of treatment of the DW1330 device, all the patients enrolled should perform 1 treatment within 1 hour after dinner 5 days a week.

Locations

Country	Name	City	State
Taiwan	Chia-Yi Christian Hospital	Chiayi City
Taiwan	Far Eastern Memorial Hospital	New Taipei City
Taiwan	Taipei Medical University-Shuang Ho Hospital,Ministry of Health and Welfare	New Taipei City
Taiwan	Chi Mei Hospital	Tainan
Taiwan	National Cheng Kung University Hospital	Tainan
Taiwan	National Taiwan University Hospital	Taipei

Sponsors (1)

Lead Sponsor	Collaborator
Taiwan Resonant Waves Research Corporation

Country where clinical trial is conducted

Taiwan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Change from baseline of inflammatory biomarkers	The exploratory objective is to detect the change of biomarkers related to body glucose level	baseline at 2 week,and 20 week
Primary	Change in HbA1c values to evaluate of the effect of DW1330	The primary study objective is to demonstrate the use of DW1330 is associated with improvement of blood glucose control, as measured by changes in glycated hemoglobin (HbA1c) values in comparison with placebo on blood glucose control parameters after 20 weeks of treatment. The time frame includes 2 weeks of screening, 20 weeks of treatment, and 2 weeks of post-treatment follow-up.	24 weeks, 2 weeks of screening, 20 weeks of treatment, and 2 weeks of post-treatment follow-up
Secondary	To evaluate the change from baseline in the percentage of subject who achieve HbA1c < 7%	compare the test group and placebo group in percentage of subjects who achieve HbA1c < 7%	24 weeks, 2 weeks of screening, and 20 weeks of treatment
Secondary	Change from baseline in FPG	Change from baseline in Fasting plasma glucose compare with test and control group	baseline at visit 2, and visit 3, 4, 5, 6, 7, 8 of treatment [up to 20 weeks]
Secondary	Evaluate the efficacy of SMBG	Change from baseline in evaluate the efficacy of self monitoring blood glucose	baseline at visit 2, and visit 4, 6, 8 of treatment [up to 20 weeks]
Secondary	Change from baseline in body weight	Change from baseline in body weight compare with test and control group	baseline at visit 2, and visit 3, 4, 5, 6, 7, 8 of treatment [up to 20 weeks]
Secondary	Change from baseline in OAD drugs description	compare the change of OAD drugs description following a 20 weeks treatment of DW1330 versus placebo	baseline at visit 2, and visit 3, 4, 5, 6, 7, 8 of treatment [up to 20 weeks]