Diabetes Mellitus Type 2NCT00233649
DIALOOG: Crestor in Patients With Diabetes Mellitus Type 2: Lowering of LDL-C Levels to New European Guidelines
An observational study of Diabetes Mellitus Type 2 and Crestor, Rosuvastatin, run by AstraZeneca at 222 sites in Netherlands.
Trial summary
The purpose of this study is to determine in DM II patients the efficacy of Crestor in obtaining the new European LDL cholesterol guidelines. Read more about this study
- Who is it for?
- Ages 18 to 70 years
- Conditions the study is for
- Diabetes Mellitus Type 2, Crestor, Rosuvastatin, LDL Cholesterol
- How many people
- 2,500 participants
- Where
- 222 sitesNetherlands
- Study dates
- May 2004to not given
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 70 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Diabetes Mellitus Type 2
Who may be able to join
- Diabetes Mellitus Type 2, LDL-C > 2,5 mmol/l, no cholesterol lowering medication used last 3 months, starts with Crestor 10 mg, permission to use patient data by AZ
Who cannot join
None listed.
Trial locations and contacts
222 sites in 1 country.
222 sites in 1 country
Netherlands222 sites
Research Site
's Gravenmoer
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's-Hertogenbosch
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Aalten
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Alkmaar
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Almelo
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Alphen aan den Rijn
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Amersfoort
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Ammerzoden
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Amstelveen
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Amsterdam
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Amsterdam-Zuidoost
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Andijk
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Apeldoorn
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Arcen
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Arkel
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Arnhem
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Assen
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Baard
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Baarle-Nassau
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Baflo
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Beek en Donk
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Benningbroek
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Bergeijk
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Bergen op Zoom
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Best
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Beverwijk
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Bilthoven
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Blaricum
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Bocholtz
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Boekel
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Boxtel
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Breda
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Brunssum
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Budel
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Burgum
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Bussum
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Callantsoog
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Capelle aan den IJssel
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Castricum
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Coevorden
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Cuijk
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Damwoude
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Delft
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Delfzijl
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Den Helder
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Deurne
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Dieren
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Dirksland
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Doesburg
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Doetinchem
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Dokkum
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Doorn
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Drachten
Research Site
Duiven
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Echt
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Ede Gld
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Eemnes
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Eersel
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Egmond aan den Hoef
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Eibergen
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Eindhoven
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Elim
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Emmeloord
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Emmen
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Enkhuizen
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Enschede
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Exloo
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Garderen
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Geldrop
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Geleen
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Goes
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Goirle
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Gorinchem
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Groningen
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Grootebroek
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Haarlem
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Hapert
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Hardenberg
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Haren
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Harskamp
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Havelte
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Heerenveen
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Heerlen
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Heeswijk-Dinther
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Heiloo
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Hellevoetsluis
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Helmond
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Hengelo Ov
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Hillegom
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Hoogeveen
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Hoogvliet
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Hoorn
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Horst
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Houten
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Huizen
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Hulst
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IJmuiden
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Joure
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Kilder
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Klazienaveen
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Koekange
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Lage Mierde
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Landgraaf
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Landsmeer
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Laren Nh
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Leek
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Leersum
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Leeuwarden
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Leiden
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Lemmer
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Leusden
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Lichtenvoorde
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Lieshout
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Limmen
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Lisse
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Lunteren
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Maarn
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Maarssen
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Maastricht
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Meerlo
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Melick
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Meppel
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Milsbeek
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Montfoort
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Moordrecht
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Musselkanaal
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Naarden
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Neede
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Nibbixwoud
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Nieuw-Buinen
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Nieuwdorp Zld
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Nieuwe Pekela
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Nieuwegein
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Nieuwendijk Nb
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Nijverdal
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Noord-Scharwoude
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Noordscheschut
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Noordwijk Zh
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Nunspeet
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Oegstgeest
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Oldenzaal
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Oost West en Middelbeers
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Oosterhout Nb
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Oss
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Oud-Beijerland
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Oude Pekela
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Oudega Gem Smallingerlnd
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Oudorp Nh
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Pijnacker
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Poeldijk
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Poortvliet
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Purmerend
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Ridderkerk
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Rijnsburg
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Rijsbergen
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Rijssen
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Rockanje
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Roosendaal
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Rotterdam
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Rozenburg Zh
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Schoonhoven
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Sint Willebrord
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Sint-Oedenrode
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Sliedrecht
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Sneek
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Sommelsdijk
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Son
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Spijkenisse
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Stadskanaal
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Steenbergen Nb
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T Zand Nh
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Ten Boer
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Ter Aar
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Terneuzen
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The Hague
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Tiel
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Tilburg
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Tuitjenhorn
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Uden
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Ulft
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Usquert
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Utrecht
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Valkenswaard
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Veenendaal
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Veghel
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Velden
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Veldhoven
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Venlo
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Venray
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Vlaardingen
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Vledder
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Vlijmen
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Voerendaal
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Volendam
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Voorburg
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Voorhout
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Voorschoten
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Vries
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Vught
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Waalre
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Wamel
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Warmond
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Warnsveld
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Weert
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Westerhaar-vriezenv Wijk
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Westervoort
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Wijchen
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Wildervank
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Winschoten
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Winterswijk
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Wognum
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Zeewolde
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Zeist
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Zevenhuizen Gn
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Zoetermeer
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Zuidhorn
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Zuidlaren
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Zutphen
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Zwaag
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Zwaagwesteinde
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Zwijndrecht
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Zwolle
About this study
The purpose of this study is to determine in DM II patients the efficacy of Crestor in obtaining the new European LDL cholesterol guidelines.
- Medical subject headings
- Diabetes Mellitus, Type 2
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Oct 2005 (estimated)
- Study startMay 2004
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Diabetes Mellitus Type 2Studies of the same condition, open and under way.
- More trials run by AstraZenecaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Time perspective
- Prospective
- Enrolment
- 2,500 participants
Sponsor and investigators
- Lead sponsor
- AstraZeneca
- Sponsor type
- Industry (pharma, biotech, devices)
- Investigators
- Astra Zeneca, Study director, AstraZeneca
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00233649
- Sponsor's protocol ID
- NL401017
- Status last verified
- Nov 2010
- First submitted
- 5 Oct 2005
- Last updated
- 19 Nov 2010
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 19 Nov 2010. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- DIALOOG: Crestor in Patients With Diabetes Mellitus Type 2: Lowering of LDL-C Levels to New European Guidelines
- ClinicalTrials.gov ID
- NCT00233649
- Acronym / sponsor ID
- NL401017
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 2,500 participants
- Lead sponsor
- AstraZenecaIndustry (pharma, biotech, devices)
- Study start
- May 2004
- First posted
- 6 Oct 2005 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to determine in DM II patients the efficacy of Crestor in obtaining the new European LDL cholesterol guidelines.
Study design
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 to 70 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Diabetes Mellitus Type 2
Key inclusion criteria (1 listed)
- Diabetes Mellitus Type 2, LDL-C > 2,5 mmol/l, no cholesterol lowering medication used last 3 months, starts with Crestor 10 mg, permission to use patient data by AZ
Key exclusion criteria (0 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Not reported in the source record.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Nov 2010.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Astra Zeneca study director
AstraZeneca
222 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Diabetes Mellitus Type 2 and Crestor, Rosuvastatin, run by AstraZeneca at 222 sites in Netherlands.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 19 Nov 2010. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 222 sites in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Nov 2010; AzTrials last refreshed its copy on 7 Nov 2026.