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Individual Patient Data Meta-analysis of CSII vs. MDI in Type 2 Diabetes

Individual Patient Data Meta-analysis of Randomised Controlled Trials Comparing Glycaemic Control During Continuous Subcutaneous Insulin Infusion vs. Multiple Daily Insulin Injections in Type 2 Diabetes Mellitus

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02910141
Enrollment
590
Registered
2016-09-21
Start date
2014-01-31
Completion date
2016-12-31
Last updated
2017-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus, Type 2

Keywords

Type 2 diabetes, Continuous subcutaneous insulin infusion, Meta-analysis, Insulin pump therapy, Multiple daily insulin injections

Brief summary

This study aims to compare glycaemic control during continuous subcutaneous insulin fusion (CSII, insulin pump therapy) and multiple daily insulin injections in type 2 diabetes and to identify patient-level characteristics that predict the best improvement in control and any change in insulin dose or other outcome.

Detailed description

The investigators will identify randomised controlled trials without language restriction that meet the inclusion criteria by searching the Cochrane database, Ovid Medline, Google Scholar and other sources. The investigators will exclude observational studies, short-term trials \<2 months duration, studies in pregnant diabetic subjects, newly diagnosed type 2 diabetes, trials in type 1 diabetes and extensions of previous studies. Data on individual participants will be obtained directly from trialists and from funding sponsors who hold the trial data and will include age, sex, duration of diabetes, treatment group, baseline and final HbA1c, baseline and final insulin dose, baseline and final BMI. A 'two-step' meta-analysis will be performed to estimate overall mean differences in HbA1c, insulin dose and weight/BMI for the trials. Then, a 'one-step' meta-regression analysis will be conducted by creating a single large dataset from the individual patient data. Determinants of final HbA1c, BMI/weight and insulin dose will be explored using Bayesian approaches with covariates that include baseline HbA1c, age, diabetes duration, BMI, insulin dose and interactions between the covariates.

Interventions

Infusion of short-acting insulin from a portable pump

Sponsors

University of Leicester
CollaboratorOTHER
University Hospital, Caen
CollaboratorOTHER
King's College London
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* RCTs of CSII vs. MDI in type 2 diabetes, study duration at least 2 months, non-pregnant

Exclusion criteria

* Type 1 diabetes, studies \<2 months duration, pregnant women, newly diagnosed type 2 diabetes and extensions of previous studies.

Design outcomes

Primary

MeasureTime frameDescription
HbA1cUp to 24 monthsDifference in glycaemic control between treatments, as measured by HbA1c

Secondary

MeasureTime frameDescription
Insulin doseUp to 24 monthsDifference in insulin dose between treatments
Weight or BMIUp to 24 monthsDifference in weight or BMI between treatments

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026