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CompletedNCT05504005Updated Aug 9, 2024

Clinical Validation of mμSORS for Noninvasive Blood Glucose Detection

An interventional study of Multi-channel Microspatial Offset Raman Scattering Spectroscopy (mμSORS) for Noninvasive Blood Glucose Detection in Diabetes Mellitus and Medical Device, sponsored by Shanghai Jiao Tong University School of Medicine. Completed at 1 site in China. Open to participants aged 30 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-08-09.

Sponsored by Shanghai Jiao Tong University School of Medicine · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
35
Allocation
Not applicable
Ages
30 Years to 60 Years
Sex
All
01

Study summary

This is a single-center, open-label, prospective study. Blood glucose was measured at different time points during oral glucose tolerance testing in healthy subjects and patients with type 2 diabetes mellitus, using both venous plasma and multi-channel microspatial offset Raman scattering spectroscopy (mμSORS). Venous plasma glucose was set as gold standard.The two measurements were collected synchronously so as to calculate the mean absolute relative difference (MARD) and the consensus error grid (CEG). Accuracy of non-invasive blood glucose testing by mμSORS will be validated. MARD for two measurement methods in different blood glucose ranges and the effect of mμSORS on safety in the patient such as adverse events will also be assessed.

Read the detailed description

In order to clinically verify the accuracy and safety of non-invasive blood glucose measurement by the mμSORS technology, and to construct a model, this study will conduct oral glucose tolerance tests on healthy subjects and patients with type 2 diabetes at different time points during the OGTT. There will be 12 points as follows: 0-min and post glucose-load 10-min,30-min,60-min,90-min,120-min,150-min,180-min,210-min,240-min,270-min, and 300-min.

02

Conditions studied

  • Diabetes Mellitus
  • Medical Device

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03

In context

Diabetes Mellitus

11,089 studies on the registry are indexed under Diabetes Mellitus; 1,319 are open to participants now.

This study's enrollment of 35 is below the median of 80 across 8,491 interventional studies indexed under Diabetes Mellitus.

Browse Diabetes Mellitus studies →

Lead sponsor

Shanghai Jiao Tong University School of Medicine is the lead sponsor of 370 studies on the registry; 107 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Male or female.
  • Aged between 30 and 60 years.
  • Fasting blood glucose (FPG) \< 6.1 mmol/L and glycated hemoglobin (HbA1c) \< 5.7% during the screening period.
  • There are no scars, obvious pigmentation and other factors that interfere with the detection of the palm skin to be tested.
  • Confirmed as healthy based on the results of physical examination, medical history, vital signs and clinical laboratory tests.
  • Fully understand the nature, significance, possible benefits, possible inconveniences or potential risks of this research, and should also understand the research procedures, be willing to complete the entire research process, and provide written consent form.

Inclusion Criteria for patients with type 2 diabetes:

  • Male or female,previously diagnosed type 2 diabetes.
  • Aged between 30 and 60 years.
  • Fasting plasma glucose ≥ 6.1 and \< 13.3 mmol/L.
  • There are no scars, obvious pigmentation and other factors that interfere with the detection of the palm skin to be tested.
  • Fully understand the nature, significance, possible benefits, possible inconveniences or potential risks of this research, and should also understand the research procedures, be willing to complete the entire research process, and provide written consent form.

Exclusion criteria

Exclusion Criteria for healthy subjects:

  • Any history of serious clinical diseases such as circulatory system, endocrine system, nervous system, digestive system, respiratory system, hematology, immunology, psychiatry or metabolic abnormality, or any other disease that can interfere with the test results, which the investigator considers significant.
  • Alcohol dependency or drug abuse.
  • Those who have participated in clinical trials of other drugs within 3 months before screening (since the last visit of the previous trial).
  • Pregnancy or lactation period.
  • Difficulty in venous blood collection or fainting of needles or blood.
  • Other circumstances that the investigator considers inappropriate to participate in the study.

Exclusion Criteria for patients with type 2 diabetes:

  • Type 1 diabetes, monogenic mutant diabetes, pancreatic damage, or secondary diabetes of other causes should be excluded.
  • Severe structural heart disease, such as congenital heart disease, rheumatic heart disease, hypertrophic or dilated cardiomyopathy, chronic congestive heart failure (NYHA≥III); acute myocardial infarction within 12 months before enrollment; history of severe liver or kidney dysfunction (eGFR \< 60 ml/min/1.73m2 calculated by MDRD formula at screening period); and mental disorders, etc.
  • With a history of acute complications of diabetes within 3 months before enrollment; or severe diabetes-related complications.
  • Alcohol dependency or drug abuse.
  • Those who have participated in clinical trials of other drugs within 3 months before screening (since the last visit of the previous trial).
  • Pregnancy or lactation period.
  • Difficulty in venous blood collection or fainting of needles or blood.
  • Other circumstances that the investigator considers inappropriate to participate in the study.
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
35 participants (actual)

Study arms

  • Experimental
    Clinical Validation of mμSORS for Noninvasive Blood Glucose Detection

    Enrolled subjects will perform oral glucose tolerance test. A measurement session of blood glucose consists of plasma sample and a measurement by mμSORS will be conducted synchronously.

    Device: Multi-channel Microspatial Offset Raman Scattering Spectroscopy (mμSORS) for Noninvasive Blood Glucose Detection

Interventions

  • DeviceMulti-channel Microspatial Offset Raman Scattering Spectroscopy (mμSORS) for Noninvasive Blood Glucose Detection

    Blood glucose of participants were measured by venous plasma and multi-channel microspatial offset Raman scattering spectroscopy (mμSORS). The two measurements were collected synchronously and analyzed.

06

What researchers measure

Primary outcomes

  1. Mean absolute relative deviation (MARD) of venous plasma glucose and glucose values measured by mμSORS at each time point of OGTT.

    Glucose will be measured using both intravenous sampling (plasma) and multi-channel microspatial offset Raman scattering spectroscopy (mμSORS) detection synchronously.

    Time frame: 2 months

  2. Consensus Error Grid (CEG) for venous plasma glucose and glucose values measured by mμSORS at each time point of OGTT.

    Glucose will be measured using both intravenous sampling (plasma) and multi-channel microspatial offset Raman scattering spectroscopy (mμSORS) detection synchronously.

    Time frame: 2 months

Secondary outcomes

  1. MARD for two measurement methods in different blood glucose ranges.

    Plasma glucose ranges 3.9-10.0 mmol/L, \<3.9 mmol/L and \>10.0 mmol/L.

    Time frame: 2 months

  2. Incidence of Treatment-Emergent Adverse Events

    Safety in the patients.

    Time frame: 2 months

07

Study locations

1 site
  • Ruijin Hospital
    Shanghai, Shanghai Municipality 200025, China
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 9, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05504005
Collaborators
Shanghai Photonic View Technology Co., Ltd.
Responsible party
Wang Weiqing (Professor, Shanghai Jiao Tong University School of Medicine) — Principal investigator
First posted
Aug 17, 2022
Start date
Oct 8, 2022
Primary completion
Dec 31, 2022
Completion
Mar 1, 2023
Last update
Aug 9, 2024

Study contacts

Weiqing Wang, Dr.
principal investigator · Ruijin Hospital

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Aug 2024. You cannot join it, but the record below documents what was studied.

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