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Comparison of Insulin Degludec With Insulin Glargine U100 for Adults With Type 1 Diabetes Crossing Multiple Time Zones.

Phase 4
Completed
Conditions
Diabetes Mellitus, Type 1
Interventions
Device: TRESIBA® FLEXTOUCH®
Device: LANTUS® SOLOSTAR® INSULIN PEN
Registration Number
NCT03668808
Lead Sponsor
Sansum Diabetes Research Institute
Brief Summary

The purpose of the proposed study is to compare insulin Degludec \[TRESIBA® (insulin degludec injection)\] with insulin Glargine U100 \[Lantus® (insulin glargine injection)\] to determine the basal insulin of choice for adults with type 1 diabetes (T1D) who fly non-stop across multiple time zones. With the introduction of Degludec as basal insulin for T1D and the opportunity to vary time of injection between 8 and 40 hours, the use of Degludec as a basal insulin may make it easier for both people living with T1D and diabetologists to plan long-haul travel compared to the use of existing basal insulins when crossing multiple time zones.The study hypothesis is that once daily Degludec as the basal insulin will provide better glycemic control for people with type 1 diabetes on multiple daily injections who are traveling non-stop across multiple time zones than once daily Glargine U100.

Detailed Description

This study will be an open-label, single center, pilot study. Participants will be randomized to either Glargine U100 or Degludec as the basal insulin, then a 2 week break, and followed by a cross-over to the other insulin. Each study period will begin in Honolulu, Hawaii (HI) (airport code HNL) with a non-stop flight to Newark, New Jersey (NJ) (EWR) lasting approximately 10 hours with a 6 hour time difference between destinations. After up to 72 hours in EWR, participants will return to Honolulu and spend up to 72 hours at that destination. Investigators plan to recruit 25 adults with established T1D currently being treated with multiple daily injections of insulin (MDI).

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
25
Inclusion Criteria
  1. Males or females ≥18 and ≤65 years of age.

  2. Type 1 diabetes mellitus (diagnosed clinically and treated with multiple daily injections of insulin) for ≥12 months.

  3. HbA1c <10% within 30 days of being enrolled in the study

  4. Current treatment with any basal insulin analogue as the once daily basal insulin given in the evening (22) and no fewer than three injections with rapid acting bolus insulin (e.g. insulin aspart, insulin lispro, or insulin glulisine) as mealtime bolus insulin therapy.

  5. No contraindication to long-haul travel.

  6. No recurrent severe hypoglycemia (more than 1 severe hypoglycemic event requiring hospitalization during the last 12 months), or hypoglycemia unawareness as judged by a score of >4 on the Gold score (23), or hospitalization for diabetic ketoacidosis during the previous 6 months.

  7. Willing and able to use a continuous glucose monitoring device (e.g. Dexcom G4).

  8. Ability to self-manage insulin therapy (verbal confirmation at screening visit) of a changed bolus insulin dose the preceding 2 months prior to screening.

  9. Ability and willingness to adhere to the protocol, including performance of self-monitored blood glucose (SMBG) readings and self-adjustment of insulin doses according to protocol.

Exclusion Criteria
  1. Current use of an insulin pump.

  2. Use within the last 3 months prior to enrollment visit 1 of any glucose-lowering drug other than insulin.

  3. Initiation or significant change of any systemic treatment which, in the investigator's opinion, could interfere with glucose metabolism, such as systemic corticosteroids, beta-blockers or monoamine oxidase inhibitors (inhaled corticosteroids allowed).

  4. Proliferative retinopathy or maculopathy requiring treatment, according to the investigator.

  5. Pregnancy, breast-feeding, the intention of becoming pregnant or not using adequate contraceptive measures.

  6. Any clinically significant disease or disorder, which in the investigator's opinion could interfere with the results of the trial.

  7. Mental incapacity, psychiatric disorder, unwillingness or language barriers precluding adequate understanding or cooperation, including subjects not able to read or write, and known or suspected abuse of alcohol, narcotics, or illicit drugs.

  8. Known or suspected allergy to any of the trial products or related products.

  9. Receipt of any investigational drug or participation in other trials within 1 month prior to Visit 1.

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Insulin DegludecInsulin DegludecSubjects with type 1 diabetes and on multiple daily injections will use basal insulin Degludec and the TRESIBA® FLEXTOUCH® pens during a long-haul flight and randomized to this arm first or second.
Insulin DegludecTRESIBA® FLEXTOUCH®Subjects with type 1 diabetes and on multiple daily injections will use basal insulin Degludec and the TRESIBA® FLEXTOUCH® pens during a long-haul flight and randomized to this arm first or second.
Insulin Glargine U100LANTUS® SOLOSTAR® INSULIN PENSubjects with type 1 diabetes and on multiple daily injections will use basal insulin Glargine U100 and the LANTUS® SOLOSTAR® INSULIN PEN during a long-haul flight and randomized to this arm first or second.
Insulin Glargine U100Insulin GlargineSubjects with type 1 diabetes and on multiple daily injections will use basal insulin Glargine U100 and the LANTUS® SOLOSTAR® INSULIN PEN during a long-haul flight and randomized to this arm first or second.
Primary Outcome Measures
NameTimeMethod
Continuous Glucose Monitoring - Time in Range (70-140 mg/dl)During the initial 24 hours local time and starting within 2 hours after arrival

Time in range (70-140 mg/dl) \[percentage of glucose readings or hours per day\] by continuous glucose monitoring (CGM) during the initial 24 hours local time (starting within 2 hours after arriving) in Newark, NJ after flying 9-10 hours West to East (from Honolulu, HI) and after the return journey from Newark to Honolulu (flying East to West).

Secondary Outcome Measures
NameTimeMethod
CGM Fasting Blood Glucose (FBG)At 0600 local time on the morning after arrival at each destination

Fasting Blood Glucose (FBG) was determined using CGM at each destination on the morning after arrival.

Liverpool Jet-Lag QuestionnaireAfter 24 and 48 hours at the destination after arrival

This is a Questionnaire about jet-lag and fatigue administered at the destinations after arrival. Jet Lag is rated on a 0-10 scale (0 - insignificant jet lag to 10 - very bad jet lag). Fatigue is rated on a scale of -5 to +5 (more fatigue to less fatigue).

Sleep Quantity Measured by ActiGraphDuring 24 hours at each destination

Measurement of sleep duration (TST - Total sleep time in minutes)

Sleep Efficiency Measured by ActiGraphDuring 24 hours at each destination

Measurement of sleep efficiency (SE% - total sleep time in minutes divided by time in bed in minutes)

Continuous Glucose Monitoring - Time in Range (70-180 mg/dl)During the initial 24 hours local time and starting within 2 hours after arrival

Time in range (70-180 mg/dl) \[percentage of glucose readings or hours per day\] by continuous glucose monitoring (CGM) during the first 24 hours after arriving in HNL and EWR (starting within 2 hours after arrival).

Mean ± SD CGM Glucose (mg/dl)In flight period of time and for 72 hours at each destination

Mean ± standard deviation of CGM glucose (mg/dl) by CGM during the flight and during the 72 hours at the destination

CGM % Time <70 mg/dlIn flight period of time and for 72 hours at each destination

% time \<70 mg/dl by CGM

CGM % Time 70-180 mg/dlIn flight period of time and for 72 hours at each destination

% time 70-180 mg/dl by CGM

CGM % Time >180 mg/dlIn flight period of time and for 72 hours at each destination

% time \>180 mg/dl by CGM

CGM - Coefficient of Variation (CV)In flight period of time and for 72 hours at each destination

Coefficient of variation of CGM values - glycemic variability (CV, %)

Trial Locations

Locations (2)

inControl Diabetes Center

🇺🇸

Honolulu, Hawaii, United States

Sansum Diabetes Research Institute

🇺🇸

Santa Barbara, California, United States

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