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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00365170
Other study ID # ANA-1474
Secondary ID
Status Completed
Phase Phase 4
First received August 10, 2006
Last updated December 20, 2016
Start date September 2002
Est. completion date April 2005

Study information

Verified date December 2016
Source Novo Nordisk A/S
Contact n/a
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)Spain: Spanish Agency of MedicinesCroatia: Ministry of Health and Social CareRussia: Pharmacological Committee, Ministry of HealthDenmark: Danish Medicines AgencyCanada: Health CanadaPoland: Ministry of HealthFinland: Finnish Medicines AgencyBulgaria: Bulgarian Drug AgencyNetherlands: Dutch Health Care InspectorateAustria: Federal Ministry for Health and WomenIsrael: Israeli Health Ministry Pharmaceutical AdministrationArgentina: Administracion Nacional de Medicamentos, Alimentos y TecnologiaIreland: Irish Medicines BoardNorway: Norwegian Medicines AgencyGreece: National Organization for MedicinesGermany: Federal Institute for Drugs and Medical DevicesUnited Kingdom: Medicines and Healthcare Products Regulatory Agency
Study type Interventional

Clinical Trial Summary

This trial was conducted in Europe, Middle East, North America and South America.

The aim of this trial was to compare the use of an intensified insulin treatment with insulin aspart (NovoRapid®) versus human insulin (Actrapid®) in pregnancy.


Recruitment information / eligibility

Status Completed
Enrollment 419
Est. completion date April 2005
Est. primary completion date April 2005
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Type 1 diabetes

- Treated with insulin for at least 12 months

- Either plan to become pregnant in the immediate future, willing to undertake pre pregnancy counselling, and has a screening HbA1c lesser than or equal to 12.0%, or

- Pregnant with normal singleton pregnancy, gestational age for at least 10 weeks at the time of randomisation, confirmed by ultrasound scan.

Exclusion Criteria:

- Previous birth of child with a major congenital malformation

- More than 2 previous multiple miscarriages or stillbirths

- Severe hyperemesis gravidarum, requiring hospitalisation, according to Investigator judgement

- Subjects being treated for infertility

- Proliferative retinopathy or maculopathy requiring acute treatment

- Drug or alcohol abuse

- Impaired renal, hepatic or cardiac function

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
human insulin

insulin aspart


Locations

Country Name City State
Argentina Novo Nordisk Investigational Site Ciudad de Buenos Aires
Argentina Novo Nordisk Investigational Site Pcia de Cordoba
Austria Novo Nordisk Investigational Site Graz
Austria Novo Nordisk Investigational Site Salzburg
Austria Novo Nordisk Investigational Site Wien
Austria Novo Nordisk Investigational Site Wien
Bulgaria Novo Nordisk Investigational Site Sofia
Canada Novo Nordisk Investigational Site Halifax Nova Scotia
Canada Novo Nordisk Investigational Site Ottawa
Canada Novo Nordisk Investigational Site St John's
Canada Novo Nordisk Investigational Site Toronto
Canada Novo Nordisk Investigational Site Toronto
Canada Novo Nordisk Investigational Site Vancouver
Canada Novo Nordisk Investigational Site Winnipeg
Croatia Novo Nordisk Investigational Site Zagreb
Denmark Novo Nordisk Investigational Site Hvidovre
Denmark Novo Nordisk Investigational Site København ø
Finland Novo Nordisk Investigational Site Helsinki
Finland Novo Nordisk Investigational Site Kuopio
Finland Novo Nordisk Investigational Site Oulu
France Novo Nordisk Investigational Site ANGERS cedex 09
France Novo Nordisk Investigational Site Avignon
France Novo Nordisk Investigational Site Bondy
France Novo Nordisk Investigational Site Brest
France Novo Nordisk Investigational Site Lille
France Novo Nordisk Investigational Site MARSEILLE Cédex 05
France Novo Nordisk Investigational Site Nantes
France Novo Nordisk Investigational Site Nimes
France Novo Nordisk Investigational Site Paris
France Novo Nordisk Investigational Site PuyRicard
France Novo Nordisk Investigational Site Strasbourg
France Novo Nordisk Investigational Site Strasbourg
France Novo Nordisk Investigational Site TOULOUSE cedex
France Novo Nordisk Investigational Site Valenciennes
Germany Novo Nordisk Investigational Site Berlin
Greece Novo Nordisk Investigational Site Athens
Greece Novo Nordisk Investigational Site Athens
Greece Novo Nordisk Investigational Site Athens
Ireland Novo Nordisk Investigational Site Dublin
Israel Novo Nordisk Investigational Site Beer Sheva
Israel Novo Nordisk Investigational Site Haifa
Israel Novo Nordisk Investigational Site Jerusalem
Israel Novo Nordisk Investigational Site Petah-Tikva
Netherlands Novo Nordisk Investigational Site Apeldoorn
Netherlands Novo Nordisk Investigational Site Brunssum
Netherlands Novo Nordisk Investigational Site Den Haag
Netherlands Novo Nordisk Investigational Site Eindhoven
Netherlands Novo Nordisk Investigational Site Roermond
Netherlands Novo Nordisk Investigational Site Rotterdam
Netherlands Novo Nordisk Investigational Site Utrecht
Norway Novo Nordisk Investigational Site Oslo
Norway Novo Nordisk Investigational Site Tromsø
Norway Novo Nordisk Investigational Site Trondheim
Poland Novo Nordisk Investigational Site Krakow
Poland Novo Nordisk Investigational Site Lodz
Poland Novo Nordisk Investigational Site Lublin
Poland Novo Nordisk Investigational Site Olsztyn
Poland Novo Nordisk Investigational Site Poznan
Poland Novo Nordisk Investigational Site Szczecin
Poland Novo Nordisk Investigational Site Warszawa
Poland Novo Nordisk Investigational Site Wroclaw
Russian Federation Novo Nordisk Investigational Site Moscow
Russian Federation Novo Nordisk Investigational Site Moscow
Russian Federation Novo Nordisk Investigational Site Saint-Petersburg
Spain Novo Nordisk Investigational Site Alicante
Spain Novo Nordisk Investigational Site Girona
Spain Novo Nordisk Investigational Site Santander
Spain Novo Nordisk Investigational Site Sevilla
United Kingdom Novo Nordisk Investigational Site Ashington
United Kingdom Novo Nordisk Investigational Site Bath
United Kingdom Novo Nordisk Investigational Site Belfast
United Kingdom Novo Nordisk Investigational Site Birmingham
United Kingdom Novo Nordisk Investigational Site Bristol
United Kingdom Novo Nordisk Investigational Site Cambridge
United Kingdom Novo Nordisk Investigational Site Edgbaston, Birmingham
United Kingdom Novo Nordisk Investigational Site Edinburgh
United Kingdom Novo Nordisk Investigational Site Exeter
United Kingdom Novo Nordisk Investigational Site Hull
United Kingdom Novo Nordisk Investigational Site Leeds
United Kingdom Novo Nordisk Investigational Site Leicester
United Kingdom Novo Nordisk Investigational Site Liverpool
United Kingdom Novo Nordisk Investigational Site London
United Kingdom Novo Nordisk Investigational Site London
United Kingdom Novo Nordisk Investigational Site Newcastle
United Kingdom Novo Nordisk Investigational Site Norfolk
United Kingdom Novo Nordisk Investigational Site Northampton
United Kingdom Novo Nordisk Investigational Site Nottingham
United Kingdom Novo Nordisk Investigational Site Oxford
United Kingdom Novo Nordisk Investigational Site Plymouth
United Kingdom Novo Nordisk Investigational Site Reading
United Kingdom Novo Nordisk Investigational Site Sheffield
United Kingdom Novo Nordisk Investigational Site Sheffield
United Kingdom Novo Nordisk Investigational Site Southampton
United Kingdom Novo Nordisk Investigational Site Stourbridge
United Kingdom Novo Nordisk Investigational Site Worcester

Sponsors (1)

Lead Sponsor Collaborator
Novo Nordisk A/S

Countries where clinical trial is conducted

Argentina,  Austria,  Bulgaria,  Canada,  Croatia,  Denmark,  Finland,  France,  Germany,  Greece,  Ireland,  Israel,  Netherlands,  Norway,  Poland,  Russian Federation,  Spain,  United Kingdom, 

References & Publications (6)

Damm P, Mersebach H, Råstam J, Kaaja R, Hod M, McCance DR, Mathiesen ER. Poor pregnancy outcome in women with type 1 diabetes is predicted by elevated HbA1c and spikes of high glucose values in the third trimester. J Matern Fetal Neonatal Med. 2014 Jan;27 — View Citation

Heller S, Damm P, Mersebach H, Skjøth TV, Kaaja R, Hod M, Durán-García S, McCance D, Mathiesen ER. Hypoglycemia in type 1 diabetic pregnancy: role of preconception insulin aspart treatment in a randomized study. Diabetes Care. 2010 Mar;33(3):473-7. doi: 1 — View Citation

Hod M, Damm P, Kaaja R, Visser GH, Dunne F, Demidova I, Hansen AS, Mersebach H; Insulin Aspart Pregnancy Study Group.. Fetal and perinatal outcomes in type 1 diabetes pregnancy: a randomized study comparing insulin aspart with human insulin in 322 subject — View Citation

Hod M, Jovanovic L. Improving outcomes in pregnant women with type 1 diabetes. Diabetes Care. 2007 Jul;30(7):e62. — View Citation

Mathiesen ER, Kinsley B, Amiel SA, Heller S, McCance D, Duran S, Bellaire S, Raben A; Insulin Aspart Pregnancy Study Group.. Maternal glycemic control and hypoglycemia in type 1 diabetic pregnancy: a randomized trial of insulin aspart versus human insulin — View Citation

McCance DR, Damm P, Mathiesen ER, Hod M, Kaaja R, Dunne F, Jensen LE, Mersebach H. Evaluation of insulin antibodies and placental transfer of insulin aspart in pregnant women with type 1 diabetes mellitus. Diabetologia. 2008 Nov;51(11):2141-3. doi: 10.100 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Relative risk of major maternal hypoglycaemia after 24 hours No
Secondary Relative risk of major and minor hypoglycaemia No
Secondary Diabetic complications No
Secondary Obstetric complications No
Secondary Other Adverse Events No
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