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Clinical Trials/NCT03513055
NCT03513055UnknownNot Applicable

Influence of Injection Technique of Premixed Insulin on Glucose Excursion in Type 2 Diabetes Mellitus Using CGMS

Nanjing First Hospital, Nanjing Medical University0 sites60 target enrollmentStarted: May 7, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
60
Primary Endpoint
the relationship between HbA1C and injection score

Study Overview

Brief Summary

To compare patients and nurses using insulin pen injector to inject premixed insulin respectively, using continuous glucose monitoring system to evaluate the glucose excursion in the two sets, study the relationship between glucose excursion and inject technique in type 2 diabetes mellitus.

Detailed Description

A total of 60 patients with type 2 diabetes who used premixed insulin will enrolled in this study.Measure their blood pressure,height and weight, BMI, liver and kidney function, blood lipids, glycosylated hemoglobin, fasting glucose, 2 hour postprandial glucose,fasting C peptide, 2 hour postprandial C peptide, fasting glucagon, 2 hour postprandial glucagon,fasting serum insulin,2 hour postprandial serum insulin,urinary albumin and insulin antibodies.The first and second days,the patients inject premixed insulin themselves,the specialist nurse graded the patient's injection technique score.The third and the fourth days the nurse change a new insulin with the same types maintain the same injection dosage.The patient need perform continuous glucose monitoring system(CGMS) for 96-hours.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •type 2 diabetes patients
  • •aged 20-80 years
  • •had been on premixed insulin and used an insulin pen for at least 3 months
  • •fasting glucose between 6.1-16 mmolL, postprandial(or random) glucose below 22.2mmol/L.
  • •No acute complications such as diabetic ketoacidosis, diabetic hypertosmolar syndrome.
  • •Subjects were able and willing to ues CGMS and eat regularly.
  • •Patients who were able to inject insulin themselves or actual injections can be accompanied.

Exclusion Criteria

  • •Insulin allergy.
  • •There has been a history of drug abuse and alcohol dependence in the past five years, or systemic hormone therapy within 3 months.
  • •Patients with poor compliance and irregular eating and exercise.
  • •Infection or stress within four weeks.
  • •Patients unable to tolerate CGMS.
  • •patients with pregnancy, breast-feeding, planning to have a baby
  • •patients with coagulopathy, serious complication,such as cardiovascular disease, end stage renal disease; and patients with severe retinopathy or other eye problems that impair their visual function, or cognitive dysfunction

Arms & Interventions

inject premixed insulin

Experimental

patients inject premixed insulin themselves then nurse inject premixed insulin

Intervention: nurse inject premixed insulin (Other)

Outcomes

Primary Outcomes

the relationship between HbA1C and injection score

Time Frame: 6 DAYS

the relationship between HbA1C and injection score

The primary endpoint was the relationship between MAGE and injection score

Time Frame: 6 DAYS

the relationship between the 24-h mean amplitude of glycemic excursions (MAGE) and injection score

the relationship between SDBG and injection score

Time Frame: 6 DAYS

the relationship between SDBG and injection score

Secondary Outcomes

  • the relation between insulin antibodies and glucose excursions(6 DAYS)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

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