Re: SURUSS trial

From: Terry J DuBose (tjdubose@juno.com)
Mon May 14 07:26:18 2001


Dr. Bui, thank you for this information.

--
Terry J DuBose

On Mon, 14 May 2001 06:42:13 -0500 The-Hung Bui <The-Hung.Bui@ks.se> writes: > At 18:43 2001-05-13 -0500, you wrote: > >Bryan, do you know where it will be published? 50,000 > pregnancies... > >can't wait to see that... is there a published description of the > trial > >protocol anywhere? > > > >Thanks for the heads-up. Please let us know when more information > is > >available. > > > >Thanks, Terry J DuBose > > > >--------------------------------------- > > > >--------------------------------------- > >On Sun, 13 May 2001 16:37:50 -0500 "Bryan Beattie" > >--------------------------------------- > ><bbeattie@globalnet.co.uk> writes: > > > THE UK SURUSS TRIAL IS COMPLETE AND IS SIMILAR TO THE FASTER > TRIAL > > > BASED ON 50,000 PREGNANCIES. IT SHOULD BE PUBLISHED IN NEXT FEWW > > > MONTHS. PRINCIPLE INVESTIGATOR PROF NICK WALD, LONDON. > > Terry, > See below. A special report will be in Health Technology Assessment, > but it > will surely be published also in a renown journal. > > Project title: SURUSS (serum, urine and ultrasound screening study) > Project > code: 93/25/05 Cost: £864,443 Grantholder: Professor Nick Wald, Head > of > Department, Dept of Environmental & Preventive Medicine, St Barts > and the > London Medical School Start date: June 1996 Estimated publication > date: Mid > 2001* *Please note that HTA publication dates include an estimate of > time > needed for report preparation and printing based on experience from > the > first year of publication > Abstract: > This is a national, observational study of first and second > trimester Downs > syndrome screening invovling 52,000 women recruited from 15 centres, > > yielding an expected 73 term pregnancies with Downs syndrome (or > about 130 > at 12 weeks). The study will assess the individual and combined > performance > of serum, urine and ultrasound markers in the first trimester of > pregnancy. > Performance will be directly compared between first and second > trimester > markers in the same women to identify the most effective screening > method. > Ultrasound nuchal translucency measurements will be taken at 10-12 > weeks > and serum and urine samples collected at this time and also at the > time of > routine screening (about 16 weeks). The samples will be stored for > analysis > at the end of the study. The size of this study and its > observational > design will ensure that the estimates of screening performance will > be > precise and unbiased. The study will specify the organisational > arrangements necessary for the implementation of the most effective > screening method. > > ***************************************************************** > The-Hung Bui, M.D. > Senior Consultant

> Director, Fetal Diagnosis Programme > Department of Molecular Medicine > Clinical Genetics Unit > Karolinska Hospital > S-171 76 Stockholm, Sweden > > phone: +46 8 517 74989 or 517 72472 (secretary) > fax: +46 8 32 77 34 > E-mail: The-Hung.Bui@ks.se > ******************************************************************

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