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Closed-loop Insulin Delivery In Type 1 Diabetes Pregnancies (CIRCUIT) (CIRCUIT)

Primary Purpose

Type 1 Diabetes Mellitus, Pregnancy Related, Glucose Metabolism Disorders

Status
Recruiting
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Tandem t:slim X2 insulin pump with Control IQ technology
Sponsored by
University of Calgary
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 1 Diabetes Mellitus focused on measuring Type 1 diabetes, pregnancy, closed-loop, clinical trial

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Between 18 and 45 years of age (inclusive)
  • A diagnosis of type 1 diabetes, as defined by Diabetes Canada, for at least 12 months
  • A viable singleton pregnancy confirmed by ultrasound, less than 14 weeks gestation
  • Currently on intensive insulin therapy (≥ 3 injections, or Continuous subcutaneous insulin infusion (CSII)
  • Willingness to use the study devices throughout the trial
  • A1c ≥ 6.5% and <10% measured any time during pregnancy prior to enrollment
  • Able to provide informed consent
  • Have access to email

Exclusion Criteria:

  • Non-type 1 diabetes
  • Current treatment with drugs known to interfere with glucose metabolism as judged by the investigator such as high dose systemic corticosteroids
  • Known or suspected allergy to insulin
  • Women with nephropathy (estimated glomerular filtration rate [eGFR] <45), severe autonomic neuropathy, uncontrolled gastroparesis or severe proliferative retinopathy, as judged by the investigator, that is likely to interfere with the normal conduct of the study and interpretation of study results
  • Total daily insulin dose <8 or >250 units/day at screening
  • Severe visual or hearing impairment, as judged by the investigator to impact treatment compliance
  • Unable to communicate effectively in English or French as judged by the investigator
  • Current use of Tandem Control IQ, DIY looping system, 670G in Auto Mode, or alternate closed-loop system as judged by the investigator
  • Any reason judged by the investigator that would likely interfere with the normal conduct of the study and interpretation of study results

Sites / Locations

  • Campbelltown Hospital
  • Royal Prince Alfred Hospital
  • Canberra Hospital
  • Royal Women's Hospital
  • Westmead Hospital
  • University of CalgaryRecruiting
  • University of ManitobaRecruiting
  • Lawson Health Research Institute
  • SunnybrookRecruiting
  • Mount Sinai HospitalRecruiting
  • University of Montreal - CHUM
  • Université LavalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Tandem t:slim X2 insulin pump with Control IQ technology plus CGM

Standard insulin delivery (multiple daily injections (MDI) or pump) and CGM

Arm Description

Participants randomized to the intervention group will be fitted with the Tandem t:slim X2 insulin pump with Control IQ technology and Dexcom G6 Continuous Glucose Monitor.

Participants randomized to the control group will be fitted with the Dexcom G6 Continuous Glucose Monitor. They will continue to use standard insulin delivery (MDI or pump) and CGM.

Outcomes

Primary Outcome Measures

Glycemic control as reflected by percent glucose time-in-range
Time in range (3.5 to 7.8 mmol/L) per day assessed by CGM glucose measurement

Secondary Outcome Measures

Percent time spent above target range per day (+/-SD)
Glucose above target range defined as glucose >7.8 mmol/L; Blood glucose will be assessed using CGM data
Percent time spent below target range per day (+/-SD)
Glucose below target range defined as glucose < 3.5 mmol/L; Blood glucose will be assessed using CGM data
Mean blood glucose measurement at 24 and 34 weeks (+/-SD)
Blood glucose measured in mmol/L and assessed using CGM data
Proportion of participants who experience maternal hypoglycemic events
Maternal hypoglycemic events defined as ≥15 minutes with CGM glucose <3.5 mmol/L [level 1] or <2.8 mmol/L [level 2]; Blood glucose will be assessed using CGM data
Glycemic variability reflected by the coefficients of variation and standard deviations of CGM data
Blood glucose measured in mmol/L and assessed using CGM data
Diabetes-related distress to the participant
Diabetes-related distress will be assessed four times during the study using the Diabetes Distress Screening Scale (DDSS17)
Fear of hypoglycemia
Fear of hypoglycemia will be assessed four times during the study using the Hypoglycemia Fear Survey Questionnaire II (HFSQ II)
Fear of hyperglycemia
Fear of hyperglycemia will be assessed four times during the study using the g. Hyperglycemia Fear in Pregnancy Survey
Sleep quality
Sleep quality will be assessed at four times during the study using the Modified Pittsburgh Sleep Quality Index (PSQI)
Health-related quality of life
Health-related quality of life will be assessed four times during the study using the Euro Quality of life questionnaire (EQ-5D-5L)
Work productivity
Work productivity will be assessed four times during the study using the Work Productivity and Activity Impairment survey
Diabetes-related distress to the partners
Diabetes-related distress to the partners will be assessed four times during the study using the Partner Diabetes Distress Scale
Proportion of participants who experience preeclampsia events
Preeclampsia is defined as pregnancy ≥20 wks gestation with SBP ≥140mmHg and/or DBP ≥90 mmHg on ≥2 occasions a minimum of 6 hrs apart and new-onset of proteinuria (defined as urinary excretion ≥0.3g protein on a 24-hr urine specimen, or ≥ 2+ by urinary dipstick, or ≥30mg protein/mmol of urinary creatinine by spot testing) OR ≥1 of the following adverse conditions: Eclampsia (Seizures in pregnancy) Elevated liver function tests (Increased AST and/or ALT >70 IU/L) Decreased platelet count <100 x 109/L Elevated serum creatinine (>80 μmol/L) Small for gestational age infant (birth weight <10th percentile)
Proportion of participants who experience gestational hypertension events
Gestational hypertension is defined as a woman ≥20 weeks gestation with a systolic blood pressure of ≥140 mm Hg and/or a diastolic blood pressure ≥90 mm Hg on ≥2 occasions a minimum of 6 hours apart without proteinuria
Proportion of participants who experience worsening chronic hypertension events
Chronic hypertension is defined as hypertension that is present at <20 weeks gestation or pre-pregnancy
Proportion of participants who have caesarean deliveries
Proportion of participants who experience preterm births
Preterm birth defined as birth occurring <37 weeks gestation
Proportion of babies born large for gestational age (>90th percentile)
Proportion of babies born small for gestational age (<10th percentile)
Mean neonatal birthweight (+/-SD)
Birthweight measured in kilograms
Comparison of birthweight z-score
Proportion of babies born with neonatal hypoglycemia
Proportion of neonates admitted to intensive care unit admission
Admission to neonatal intensive care unit admission defined as admission of 24 hours or more
Proportion of participants who experienced pregnancy loss or miscarriage (< 20 weeks, stillbirth ≥20 weeks, neonatal loss up to 28 days)
Proportion of participants who experience episodes of severe hypoglycemia
Severe hypoglycemia defined as a hypoglycemic episode requiring assistance from another person.
Proportion of participants who experience episodes of diabetic ketoacidosis
Diabetic ketoacidosis (DKA) is defined as an episode with elevated plasma ketones which can be categorized as possible DKA (mild/ self- treated [plasma ketones 0.6 - 1.5mmol/L], moderate/self-treated (plasma ketones > 1.5mmol/L which resolves without hospital admission), or capillary blood ketones >3.0 mol/L without an anion gap of > 15 with admission to hospital for another reason [i.e. prevention of DKA]) or confirmed DKA (severe, with either plasma ketones > 3.0mmol/L or positive serum ketones with an anion gap (Na -(CI+HC03) > 15 and requiring hospital admission for IV fluids and IV insulin to correct the abnormal metabolic state).
Proportion of participants who experience device-related adverse events
Device-related adverse events include skin reactions and insulin delivery failures.

Full Information

First Posted
April 28, 2021
Last Updated
August 29, 2023
Sponsor
University of Calgary
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1. Study Identification

Unique Protocol Identification Number
NCT04902378
Brief Title
Closed-loop Insulin Delivery In Type 1 Diabetes Pregnancies (CIRCUIT)
Acronym
CIRCUIT
Official Title
Closed-loop Insulin Delivery by Glucose Responsive Computer Algorithms In Type 1 Diabetes Pregnancies (CIRCUIT)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 15, 2021 (Actual)
Primary Completion Date
January 2026 (Anticipated)
Study Completion Date
January 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Calgary

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This trial will assess the efficacy of the Tandem t:slim X2 insulin pump with Control IQ technology compared with standard insulin delivery plus CGM in pregnant women with type 1 diabetes.
Detailed Description
Pregnant women with type 1 diabetes (T1D) require normal or near normal glucose in order to reduce the risks of birth defects, stillbirth, increased birthweight, neonatal hypoglycemia, neonatal death, preterm delivery and preeclampsia. Reducing maternal glucose is extremely difficult due to an increased risk of maternal hypoglycemia. Only 14% of T1D pregnancies achieve pregnancy guideline recommended glucose control, leading to complications related to high maternal glucose exposure in roughly half of newborns. Maintaining recommended maternal glucose levels during pregnancy reduces the risk of adverse neonatal outcomes to those similar in pregnancies unaffected by T1D. Most insulin pumps in use today are open-loop systems, which means that the user must program the pump to deliver a pre-set amount of insulin. These insulin delivery methods (MDI and open-loop pumps) are usually inadequate to achieve the optimal glucose control necessary for T1D pregnancies and they impart a large time, effort and emotional burden. Closed-loop systems have been found to be effective in improving glucose control outside of pregnancy when studied in children and adults. A new hybrid closed-loop system, the Tandem t:slim X2 insulin pump with Control IQ technology, recently became commercially available. Trials have demonstrated the efficacy of the Control IQ algorithm for non-pregnant adults and children. Pregnant women were not included in these trials. The investigators propose the first randomized controlled trial to evaluate the Tandem t:slim X2 insulin pump with Control IQ technology versus standard insulin delivery (MDI or pump) and CGM in pregnant women with T1D. In this trial, the investigators will assess the efficacy of the Tandem t:slim X2 insulin pump with Control IQ technology compared with standard insulin delivery plus CGM in pregnant women with type 1 diabetes. We are grateful to Tandem Diabetes Care and Dexcom for in-kind donations to this investigator initiated study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes Mellitus, Pregnancy Related, Glucose Metabolism Disorders, Metabolic Disease, Endocrine System Diseases
Keywords
Type 1 diabetes, pregnancy, closed-loop, clinical trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Tandem t:slim X2 insulin pump with Control IQ technology plus CGM
Arm Type
Experimental
Arm Description
Participants randomized to the intervention group will be fitted with the Tandem t:slim X2 insulin pump with Control IQ technology and Dexcom G6 Continuous Glucose Monitor.
Arm Title
Standard insulin delivery (multiple daily injections (MDI) or pump) and CGM
Arm Type
No Intervention
Arm Description
Participants randomized to the control group will be fitted with the Dexcom G6 Continuous Glucose Monitor. They will continue to use standard insulin delivery (MDI or pump) and CGM.
Intervention Type
Device
Intervention Name(s)
Tandem t:slim X2 insulin pump with Control IQ technology
Intervention Description
The intervention group will be fitted with the Tandem t:slim X2 insulin pump with Control IQ technology during pregnancy.
Primary Outcome Measure Information:
Title
Glycemic control as reflected by percent glucose time-in-range
Description
Time in range (3.5 to 7.8 mmol/L) per day assessed by CGM glucose measurement
Time Frame
16 weeks until 34 weeks gestation
Secondary Outcome Measure Information:
Title
Percent time spent above target range per day (+/-SD)
Description
Glucose above target range defined as glucose >7.8 mmol/L; Blood glucose will be assessed using CGM data
Time Frame
16 weeks gestation until delivery of neonate
Title
Percent time spent below target range per day (+/-SD)
Description
Glucose below target range defined as glucose < 3.5 mmol/L; Blood glucose will be assessed using CGM data
Time Frame
16 weeks gestation until delivery of neonate
Title
Mean blood glucose measurement at 24 and 34 weeks (+/-SD)
Description
Blood glucose measured in mmol/L and assessed using CGM data
Time Frame
24 and 34 weeks gestation
Title
Proportion of participants who experience maternal hypoglycemic events
Description
Maternal hypoglycemic events defined as ≥15 minutes with CGM glucose <3.5 mmol/L [level 1] or <2.8 mmol/L [level 2]; Blood glucose will be assessed using CGM data
Time Frame
16 weeks gestation until delivery of neonate
Title
Glycemic variability reflected by the coefficients of variation and standard deviations of CGM data
Description
Blood glucose measured in mmol/L and assessed using CGM data
Time Frame
16 weeks gestation until delivery of neonate
Title
Diabetes-related distress to the participant
Description
Diabetes-related distress will be assessed four times during the study using the Diabetes Distress Screening Scale (DDSS17)
Time Frame
7-13 weeks + 6 days gestation, 24 weeks gestation, 34 weeks gestation, 6 weeks postpartum
Title
Fear of hypoglycemia
Description
Fear of hypoglycemia will be assessed four times during the study using the Hypoglycemia Fear Survey Questionnaire II (HFSQ II)
Time Frame
7-13 weeks + 6 days gestation, 24 weeks gestation, 34 weeks gestation, 6 weeks postpartum
Title
Fear of hyperglycemia
Description
Fear of hyperglycemia will be assessed four times during the study using the g. Hyperglycemia Fear in Pregnancy Survey
Time Frame
7-13 weeks + 6 days gestation, 24 weeks gestation, 34 weeks gestation, 6 weeks postpartum
Title
Sleep quality
Description
Sleep quality will be assessed at four times during the study using the Modified Pittsburgh Sleep Quality Index (PSQI)
Time Frame
7-13 weeks + 6 days gestation, 24 weeks gestation, 34 weeks gestation, 6 weeks postpartum
Title
Health-related quality of life
Description
Health-related quality of life will be assessed four times during the study using the Euro Quality of life questionnaire (EQ-5D-5L)
Time Frame
7-13 weeks + 6 days gestation, 24 weeks gestation, 34 weeks gestation, 6 weeks postpartum
Title
Work productivity
Description
Work productivity will be assessed four times during the study using the Work Productivity and Activity Impairment survey
Time Frame
7-13 weeks + 6 days gestation, 24 weeks gestation, 34 weeks gestation, 6 weeks postpartum
Title
Diabetes-related distress to the partners
Description
Diabetes-related distress to the partners will be assessed four times during the study using the Partner Diabetes Distress Scale
Time Frame
7-13 weeks + 6 days gestation, 24 weeks gestation, 34 weeks gestation, 6 weeks postpartum
Title
Proportion of participants who experience preeclampsia events
Description
Preeclampsia is defined as pregnancy ≥20 wks gestation with SBP ≥140mmHg and/or DBP ≥90 mmHg on ≥2 occasions a minimum of 6 hrs apart and new-onset of proteinuria (defined as urinary excretion ≥0.3g protein on a 24-hr urine specimen, or ≥ 2+ by urinary dipstick, or ≥30mg protein/mmol of urinary creatinine by spot testing) OR ≥1 of the following adverse conditions: Eclampsia (Seizures in pregnancy) Elevated liver function tests (Increased AST and/or ALT >70 IU/L) Decreased platelet count <100 x 109/L Elevated serum creatinine (>80 μmol/L) Small for gestational age infant (birth weight <10th percentile)
Time Frame
16 weeks gestation until delivery of neonate
Title
Proportion of participants who experience gestational hypertension events
Description
Gestational hypertension is defined as a woman ≥20 weeks gestation with a systolic blood pressure of ≥140 mm Hg and/or a diastolic blood pressure ≥90 mm Hg on ≥2 occasions a minimum of 6 hours apart without proteinuria
Time Frame
16 weeks gestation until delivery of neonate
Title
Proportion of participants who experience worsening chronic hypertension events
Description
Chronic hypertension is defined as hypertension that is present at <20 weeks gestation or pre-pregnancy
Time Frame
16 weeks gestation until delivery of neonate
Title
Proportion of participants who have caesarean deliveries
Time Frame
16 weeks gestation until delivery of neonate
Title
Proportion of participants who experience preterm births
Description
Preterm birth defined as birth occurring <37 weeks gestation
Time Frame
Delivery of neonate to 6 weeks postpartum
Title
Proportion of babies born large for gestational age (>90th percentile)
Time Frame
Delivery of neonate
Title
Proportion of babies born small for gestational age (<10th percentile)
Time Frame
Delivery of neonate
Title
Mean neonatal birthweight (+/-SD)
Description
Birthweight measured in kilograms
Time Frame
Delivery of neonate
Title
Comparison of birthweight z-score
Time Frame
Delivery of neonate
Title
Proportion of babies born with neonatal hypoglycemia
Time Frame
Delivery of neonate
Title
Proportion of neonates admitted to intensive care unit admission
Description
Admission to neonatal intensive care unit admission defined as admission of 24 hours or more
Time Frame
Delivery of neonate to 6 weeks postpartum
Title
Proportion of participants who experienced pregnancy loss or miscarriage (< 20 weeks, stillbirth ≥20 weeks, neonatal loss up to 28 days)
Time Frame
7-13 weeks until delivery of neonate + up to 28 days
Title
Proportion of participants who experience episodes of severe hypoglycemia
Description
Severe hypoglycemia defined as a hypoglycemic episode requiring assistance from another person.
Time Frame
7-13 weeks + 6 days gestation until delivery of neonate
Title
Proportion of participants who experience episodes of diabetic ketoacidosis
Description
Diabetic ketoacidosis (DKA) is defined as an episode with elevated plasma ketones which can be categorized as possible DKA (mild/ self- treated [plasma ketones 0.6 - 1.5mmol/L], moderate/self-treated (plasma ketones > 1.5mmol/L which resolves without hospital admission), or capillary blood ketones >3.0 mol/L without an anion gap of > 15 with admission to hospital for another reason [i.e. prevention of DKA]) or confirmed DKA (severe, with either plasma ketones > 3.0mmol/L or positive serum ketones with an anion gap (Na -(CI+HC03) > 15 and requiring hospital admission for IV fluids and IV insulin to correct the abnormal metabolic state).
Time Frame
7-13 weeks + 6 days gestation until delivery of neonate
Title
Proportion of participants who experience device-related adverse events
Description
Device-related adverse events include skin reactions and insulin delivery failures.
Time Frame
7-13 weeks + 6 days gestation until delivery of neonate

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Between 18 and 45 years of age (inclusive) A diagnosis of type 1 diabetes, as defined by Diabetes Canada, for at least 12 months A viable singleton pregnancy confirmed by ultrasound, less than 14 weeks gestation Currently on intensive insulin therapy (≥ 3 injections, or Continuous subcutaneous insulin infusion (CSII) Willingness to use the study devices throughout the trial A1c ≥ 6.5% and <10% measured any time during pregnancy prior to enrollment Able to provide informed consent Have access to email Exclusion Criteria: Non-type 1 diabetes Current treatment with drugs known to interfere with glucose metabolism as judged by the investigator such as high dose systemic corticosteroids Known or suspected allergy to insulin Women with nephropathy (estimated glomerular filtration rate [eGFR] <45), severe autonomic neuropathy, uncontrolled gastroparesis or severe proliferative retinopathy, as judged by the investigator, that is likely to interfere with the normal conduct of the study and interpretation of study results Total daily insulin dose <8 or >250 units/day at screening Severe visual or hearing impairment, as judged by the investigator to impact treatment compliance Unable to communicate effectively in English or French as judged by the investigator Current use of Tandem Control IQ, DIY looping system, 670G in Auto Mode, or alternate closed-loop system as judged by the investigator Any reason judged by the investigator that would likely interfere with the normal conduct of the study and interpretation of study results
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lois Donovan, MD
Phone
1-403-955-8358
Email
lois.donovan@ahs.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Denice Feig, MD
Phone
1-416-586-8590
Email
d.feig@utoronto.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lois Donovan, MD
Organizational Affiliation
University of Calgary
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Denice Feig, MD
Organizational Affiliation
MOUNT SINAI HOSPITAL
Official's Role
Principal Investigator
Facility Information:
Facility Name
Campbelltown Hospital
City
Campbelltown
ZIP/Postal Code
2560
Country
Australia
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
David Simmons, MD
Email
da.simmons@westernsydney.edu.au
Facility Name
Royal Prince Alfred Hospital
City
Camperdown
Country
Australia
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Arianne Sweeting
Email
arianne.sweeting@sydney.edu.au
Facility Name
Canberra Hospital
City
Garran
Country
Australia
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christopher Nolan
Facility Name
Royal Women's Hospital
City
Parkville
Country
Australia
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sarah Price
Email
sarah.price@unimelb.edu.au
Facility Name
Westmead Hospital
City
Westmead
Country
Australia
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wah Cheung
Email
wah.cheung@health.nsw.gov.au
Facility Name
University of Calgary
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2T 5C7
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lois Donovan, MD
Phone
403-955-8358
Email
lois.donovan@ahs.ca
First Name & Middle Initial & Last Name & Degree
Lois Donovan, MD
Facility Name
University of Manitoba
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R3E 3P4
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jennifer Yamamoto, MD
Email
jennifer.yamamoto@umanitoba.ca
Facility Name
Lawson Health Research Institute
City
London
State/Province
Ontario
ZIP/Postal Code
N6C 2R5
Country
Canada
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Selina Liu, MD
Email
selina.liu@sjhc.london.on.ca
Facility Name
Sunnybrook
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4N 3M5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ilana Halperin, MD
Email
ilana.halperin@sunnybrook.ca
Facility Name
Mount Sinai Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5T 3L9
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Denice Feig, MD
Phone
416-586-8590
Email
d.feig@utoronto.ca
Facility Name
University of Montreal - CHUM
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H2X 3J4
Country
Canada
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ariane Godbout, MD
Email
ariane.godbout.med@ssss.gouv.qc.ca
Facility Name
Université Laval
City
Quebec City
State/Province
Quebec
ZIP/Postal Code
G1V 4G2
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Patricia Lemieux, MD
Email
patricia.lemieux.3@ulaval.ca

12. IPD Sharing Statement

Plan to Share IPD
No
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19675195
Citation
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Results Reference
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24705609
Citation
Feig DS, Hwee J, Shah BR, Booth GL, Bierman AS, Lipscombe LL. Trends in incidence of diabetes in pregnancy and serious perinatal outcomes: a large, population-based study in Ontario, Canada, 1996-2010. Diabetes Care. 2014 Jun;37(6):1590-6. doi: 10.2337/dc13-2717. Epub 2014 Apr 4.
Results Reference
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PubMed Identifier
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Citation
Evers IM, de Valk HW, Visser GH. Risk of complications of pregnancy in women with type 1 diabetes: nationwide prospective study in the Netherlands. BMJ. 2004 Apr 17;328(7445):915. doi: 10.1136/bmj.38043.583160.EE. Epub 2004 Apr 5.
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Murphy HR, Roland JM, Skinner TC, Simmons D, Gurnell E, Morrish NJ, Soo SC, Kelly S, Lim B, Randall J, Thompsett S, Temple RC. Effectiveness of a regional prepregnancy care program in women with type 1 and type 2 diabetes: benefits beyond glycemic control. Diabetes Care. 2010 Dec;33(12):2514-20. doi: 10.2337/dc10-1113.
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Citation
Gupton A, Heaman M, Cheung LW. Complicated and uncomplicated pregnancies: women's perception of risk. J Obstet Gynecol Neonatal Nurs. 2001 Mar-Apr;30(2):192-201. doi: 10.1111/j.1552-6909.2001.tb01535.x.
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Closed-loop Insulin Delivery In Type 1 Diabetes Pregnancies (CIRCUIT)

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