Status:
COMPLETED
Cascade CGM 15-day Performance Assessment
Lead Sponsor:
WaveForm Technologies Inc.
Conditions:
Continuous Glucose Monitoring
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
To validate the feasibility of a 15-day wear period of the Cascade CGM system
Detailed Description
To assess a 15-day wear period for the Cascade CGM. This study includes ten subjects who will interface with the system and take finger stick BGM glucose values for calibration. The wear period includ...
Eligibility Criteria
Inclusion
- • Signed informed consent form
- Diagnosis of type 1 or type 2 (on insulin therapy) diabetes mellitus for at least 6 months
- 18 years of age or older
- Currently self-monitoring capillary blood glucose (on average at least three times per day or more) or on a CGM for at least three months
- Willing to have blood glucose levels manipulated into high and low glucose levels during in clinic days if deemed appropriate per the protocol based on insulin use.
- Willing to follow all study procedures, including attending all clinic visits during which a venous line will be inserted for blood sampling, wearing CGM sensors for entire study, performing fingertip glucose tests for self-monitoring and calibration, and keeping a diary of activities.
- Be willing to wear two investigational CGM devices.
Exclusion
- • Known allergy to medical grade adhesives
- Magnetic Resonance Imaging (MRI) scheduled during CGM sensor wear period
- Persons with type 2 diabetes using diet and exercise only for diabetes management
- Used an investigational drug within 30 days prior to study entry
- Hematocrit \< 32% (obtained during screening)
- Inadequate veins (in the opinion of the investigator) or known contraindication to placement of a dedicated peripheral line for venous blood withdrawal
- Symptomatic coronary artery disease with a history of angina, or history of a myocardial infarction or coronary intervention (e.g., percutaneous transluminal coronary angioplasty \[PTCA\], stent placement), or coronary artery bypass graft (CABG) within the past six months
- Diagnosis of the following diabetic autonomic neuropathies: orthostatic hypotension, heart rate anomalies, gastroparesis
- Cerebrovascular incident within the past six month
- History or presence of eczema, psoriasis, atopic or contact dermatitis
- Subject is pregnant at the start of the study.
- Current use or within one-week exposure to topical medications at the proposed insertion sites
- Seizure disorder (epilepsy)
- Malignancy within the past five years, except basal cell or squamous cell skin cancers
- Major surgical operation within 30 days prior to screening
- Other medical conditions that would pose safety concerns, interfere with study conduct or seriously compromise study integrity (reason for exclusion will be clearly documented by investigator or designee)
Key Trial Info
Start Date :
September 28 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 13 2019
Estimated Enrollment :
10 Patients enrolled
Trial Details
Trial ID
NCT04099043
Start Date
September 28 2019
End Date
October 13 2019
Last Update
April 6 2020
Active Locations (1)
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1
Splošna bolnišnica Celje
Celje, Slovenia