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Dirk Simon

FARSOON Europe GmbH, former BASF3DPrint Solutions -B3DPS

Dr. Dirk Simon works in BASF since 5 years, and pushed the topic "3D-Printing at BASF" from Scouting thru New Business Incubation into the Business Build-up. He holds a PhD-degree in Polymer Science and has 20 years working experiences in Applications of Plastics, Marketing Sales, and Purchasing in various chemical companies. As the Global Business Director, he is responsible for the Business Development of BASF 3D-P solutions, including 3D-P application technology.

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Joachim Stumpp is architect and director of the raumPROBE Stuttgart. raumPROBE is the agency for consulting and research in the field of materials for architecture and design. Therefore his interests regarding technology and design are always focused on material innovations.

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IFA3D Medical Solutions GmbH

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Studio Wagner:Design is a creative agency based in Frankfurt/Main for product development, UX design and strategic planning. Work areas are in the fields of electronics entertainment, IoT, sports equipment and others. The company operates according to its own methodology of design thinking and strategic planning. 3D printing (external and in-house) belongs to the performance of the studio from the beginning, turning from rapid prototyping to generative manufacturing.

The German Design Club (DDC) was founded in 1989. DDC is an initiative that combines "good design" as well as "good designers" from design, architecture, media and those who are committed to this. Wolf Wagner is Director of the German Design Club. His aim is to promote the dialogue between creative developers and representatives from engineering, industry, trade.

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Related Story: 10 best moments from Scott Kelly's year in space
Related Story: 'Like camping for a year': NASA astronaut looks forward to coming home
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One twin went to space, the other stayed on Earth — and the year they spent apart seems to have left its mark on their DNA.

Key points:

As part of NASA's Twins Study, astronaut Scott Kelly was sent to the International Space Station while his identical brother Mark, also an astronaut, stayed on Earth.

NASA created the study to research how one year in space could affect the human body.

Researchers took biological samples from Scott before, during and after his mission and then compared them to Mark's samples.

NASA says it will publish the results in a formal study later this year. But the space agency has Dolce E Gabbana Womens Black L latest collections cheap nicekicks cheap sale professional cheap for sale sast cheap price zgXji7EQJ2
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In particular, while the activity of a few thousand genes was altered during Scott's space station sojourn — no great surprise, given the stress placed on his body — some 7 per cent of those genes did not return to normal expression levels, even six months after landing.

NASA has also learned that Scott's chromosomes lengthened during his time in space. Inside his white blood cells, the protective caps or "telomeres" at the end of each chromosome expanded.

He also returned to earth five centimetres taller.

At the time, NASA spokesman Jeff Williams told CNN that astronauts got taller in space as the spine elongated.

"But they return to pre-flight height after a short time back on Earth," he said.

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This article has Open Peer Review reports available.

How does Open Peer Review work?

Trials 2009 10 :46

https://doi.org/10.1186/1745-6215-10-46

© Wu et al.; licensee BioMed Central Ltd.2009

Received: 17September2008

Accepted: 02July2009

Published: 02July2009

Open Peer Review reports

Abstract

Background

The approximately 1100 medical journals now active in China are publishing a rapidly increasing number of research reports, including many studies identified by their authors as randomized controlled trials. It has been noticed that these reports mostly present positive results, and their quality and authenticity have consequently been called into question. We investigated the adequacy of randomization of clinical trials published in recent years in China to determine how many of them met acceptable standards for allocating participants to treatment groups.

Methods

The China National Knowledge Infrastructure electronic database was searched for reports of randomized controlled trials on 20 common diseases published from January 1994 to June 2005. From this sample, a subset of trials that appeared to have used randomization methods was selected. Twenty-one investigators trained in the relevant knowledge, communication skills and quality control issues interviewed the original authors of these trials about the participant randomization methods and related quality-control features of their trials.

Results

From an initial sample of 37,313 articles identified in the China National Knowledge Infrastructure database, we found 3137 apparent randomized controlled trials. Of these, 1452 were studies of conventional medicine (published in 411 journals) and 1685 were studies of traditional Chinese medicine (published in 352 journals). Interviews with the authors of 2235 of these reports revealed that only 207 studies adhered to accepted methodology for randomization and could on those grounds be deemed authentic randomized controlled trials (6.8%, 95% confidence interval 5.9–7.7). There was no statistically significant difference in the rate of authenticity between randomized controlled trials of traditional interventions and those of conventional interventions. Randomized controlled trials conducted at hospitals affiliated to medical universities were more likely to be authentic than trials conducted at level 3 and level 2 hospitals (relative risk 1.58, 95% confidence interval 1.18–2.13, and relative risk 14.42, 95% confidence interval 9.40–22.10, respectively). The likelihood of authenticity was higher in level 3 hospitals than in level 2 hospitals (relative risk 9.32, 95% confidence interval 5.83–14.89). All randomized controlled trials of pre-market drug clinical trial were authentic by our criteria. Of the trials conducted at university-affiliated hospitals, 56.3% were authentic (95% confidence interval 32.0–81.0).

Conclusion

Most reports of randomized controlled trials published in some Chinese journals lacked an adequate description of randomization. Similarly, most so called 'randomized controlled trials' were not real randomized controlled trials owing toa lack of adequate understanding on the part of the authors of rigorous clinical trial design. All randomized controlled trials of pre-market drug clinical trial included in this research were authentic. Randomized controlled trials conducted by authors in high level hospitals, especially in hospitals affiliated to medical universities had a higher rate of authenticity. That so many non-randomized controlled trials were published as randomized controlled trials reflected the fact that peer review needs to be improved and a good practice guide for peer review including how to identify the authenticity of the study urgently needs to be developed.

Traditional Chinese Medicine Measle Allocation Concealment Conventional Medicine Random Sequence Generation

A systematic review has found that some countries, including China, report unusually high proportions of positive results in published randomized controlled trials (RCTs) [ 1 ]. One factor that may contribute to this effect is selection bias. It has been shown that inadequate randomization approaches result in estimates of treatment effects that are more favorable than those derived from properly randomized trials [ Rag amp; Bone Leather Oliver Ankle Boots free shipping best seller NJi0ZZ
, 3 ]. A systematic review conducted by Gu . [ 4 ] provides insight into this methodological shortcoming in trials conducted in China. In an effort to evaluate the benefits and harms of Chinese medicinal herbs in the treatment of measles, they identified a total of 28 reports of randomized trials that appeared to meet their eligibility criteria. As part of their review they conducted telephone interviews of 19 corresponding or first authors and discovered that the study authors had used inappropriate methods to generate the random sequence list and had not adequately concealed the participant allocation. These studies could therefore not be regarded as authentic randomized trials. Although this is a disturbing result, it is difficult to assess whether it represents a misunderstanding on the part of a few researchers about fundamental methodological issues in the conduct of randomized trials, or whether it reflects a larger problem prevalent among trials conducted throughout China. In this study, we therefore aimed to investigate the adequacy of randomization of RCTs published in Chinese journals and the extent of the authenticity of randomized trials using a large cross-sectional sample of the Chinese literature.

Twenty-one investigators searched the China National Knowledge Infrastructure electronic database for the period January 1994 to June 2005, for trials written by Chinese researchers and published in Chinese journals on a convenient sample of 20 common diseases. Any trial described by the authors as an RCT or that claimed to have used random sequence generation or allocation concealment was considered eligible.

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