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  <title type="text">PLoS Hubs for Clinical Trials: New Articles</title>
  
  <author>
    <name>PLoS</name>
    <uri>http://clinicaltrials.ploshubs.org/</uri>
    <email>webmaster@plos.org</email>
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  <subtitle>Publishing science</subtitle>
  <id>info:doi/10.1371/feed.phct</id>
  <rights>This work is licensed under a Creative Commons Attribution-Share Alike 3.0 License</rights>
  <updated>2008-11-20T12:04:03Z</updated>
  <link rel="self" href="http://clinicaltrials.ploshubs.org/feed/NewArticles" type="application/atom+xml" /><feedburner:feedFlare href="http://add.my.yahoo.com/rss?url=http%3A%2F%2Fclinicaltrials.ploshubs.org%2Ffeed%2FNewArticles" src="http://us.i1.yimg.com/us.yimg.com/i/us/my/addtomyyahoo4.gif">Subscribe with My Yahoo!</feedburner:feedFlare><feedburner:feedFlare href="http://www.newsgator.com/ngs/subscriber/subext.aspx?url=http%3A%2F%2Fclinicaltrials.ploshubs.org%2Ffeed%2FNewArticles" src="http://www.newsgator.com/images/ngsub1.gif">Subscribe with NewsGator</feedburner:feedFlare><feedburner:feedFlare href="http://feeds.my.aol.com/add.jsp?url=http%3A%2F%2Fclinicaltrials.ploshubs.org%2Ffeed%2FNewArticles" src="http://o.aolcdn.com/favorites.my.aol.com/webmaster/ffclient/webroot/locale/en-US/images/myAOLButtonSmall.gif">Subscribe with My AOL</feedburner:feedFlare><feedburner:feedFlare href="http://www.rojo.com/add-subscription?resource=http%3A%2F%2Fclinicaltrials.ploshubs.org%2Ffeed%2FNewArticles" src="http://blog.rojo.com/RojoWideRed.gif">Subscribe with Rojo</feedburner:feedFlare><feedburner:feedFlare href="http://www.bloglines.com/sub/http://clinicaltrials.ploshubs.org/feed/NewArticles" src="http://www.bloglines.com/images/sub_modern11.gif">Subscribe with Bloglines</feedburner:feedFlare><feedburner:feedFlare href="http://www.netvibes.com/subscribe.php?url=http%3A%2F%2Fclinicaltrials.ploshubs.org%2Ffeed%2FNewArticles" src="http://www.netvibes.com/img/add2netvibes.gif">Subscribe with Netvibes</feedburner:feedFlare><feedburner:feedFlare href="http://fusion.google.com/add?feedurl=http%3A%2F%2Fclinicaltrials.ploshubs.org%2Ffeed%2FNewArticles" src="http://buttons.googlesyndication.com/fusion/add.gif">Subscribe with Google</feedburner:feedFlare><feedburner:feedFlare href="http://www.pageflakes.com/subscribe.aspx?url=http%3A%2F%2Fclinicaltrials.ploshubs.org%2Ffeed%2FNewArticles" src="http://www.pageflakes.com/ImageFile.ashx?instanceId=Static_4&amp;fileName=ATP_blu_91x17.gif">Subscribe with Pageflakes</feedburner:feedFlare><entry>
    <title>Controlling Tungiasis in an Impoverished Community: An Intervention Study</title>
    <link rel="alternate" href="http://feeds.feedburner.com/~r/plosclinicaltrials/NewArticles/~3/434631240/info%3Adoi%2F10.1371%2Fjournal.pntd.0000324" />
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    <author>
      <name>Daniel Pilger et al.</name>
    </author>
    <id>info:doi/10.1371/journal.pntd.0000324</id>
    <updated>2008-10-22T07:00:00Z</updated>
    <published>2008-10-22T07:00:00Z</published>
    <content type="html">&lt;p&gt;by Daniel Pilger, Stefan Schwalfenberg, Jörg Heukelbach, Lars Witt, Norbert Mencke, Adak Khakban, Hermann Feldmeier&lt;/p&gt;
Author Summary

&lt;p xmlns:xs="http://www.w3.org/2001/XMLSchema" xmlns:fn="http://www.w3.org/2005/xpath-functions" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:util="http://dtd.nlm.nih.gov/xsl/util" xmlns:fo="http://www.w3.org/1999/XSL/Format" xmlns:mml="http://www.w3.org/1998/Math/MathML"&gt;Tungiasis is a disease caused by the sand flea &lt;i&gt;Tunga penetrans&lt;/i&gt;, a parasite prevalent in many impoverished communities in developing countries. The female sand flea penetrates into the skin of animals and humans where it grows rapidly in size, feeds on the host's blood, produces eggs which are expelled into the environment, and eventually dies in situ. The lesions become frequently superinfected and the infestation is associated with considerable morbidity. Clearly, tungiasis is a neglected disease of neglected populations. We investigated the impact of a package of intervention measures targeted against on-host and off-host stages of &lt;i&gt;T. penetrans&lt;/i&gt; in a fishing community in Northeast Brazil. These measures decreased disease occurrence only temporarily, but had a sustained effect on the intensity of the infestation. Since infestation intensity and morbidity are correlated, presumably the intervention also lowered tungiasis-associated morbidity. Control measures similar to the ones used in this study may help to effectively control tungiasis in impoverished communities.&lt;/p&gt;&lt;img src="http://feeds.feedburner.com/~r/plosclinicaltrials/NewArticles/~4/434631240" height="1" width="1"/&gt;</content>
  <feedburner:origLink>http://clinicaltrials.ploshubs.org/article/info%3Adoi%2F10.1371%2Fjournal.pntd.0000324</feedburner:origLink></entry>
  <entry>
    <title>The Diaphragm and Lubricant Gel for Prevention of Cervical Sexually Transmitted Infections: Results of a Randomized Controlled Trial</title>
    <link rel="alternate" href="http://feeds.feedburner.com/~r/plosclinicaltrials/NewArticles/~3/434631242/info%3Adoi%2F10.1371%2Fjournal.pone.0003488" />
    <link rel="related" type="text/xml" href="http://clinicaltrials.ploshubs.org/article/fetchObjectAttachment.action?uri=info:doi/10.1371/journal.pone.0003488&amp;representation=XML" />
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    <author>
      <name>Gita Ramjee et al.</name>
    </author>
    <id>info:doi/10.1371/journal.pone.0003488</id>
    <updated>2008-10-22T07:00:00Z</updated>
    <published>2008-10-22T07:00:00Z</published>
    <content type="html">&lt;p&gt;by Gita Ramjee, Ariane van der Straten, Tsungai Chipato, Guy de Bruyn, Kelly Blanchard, Stephen Shiboski, Helen Cheng, Elizabeth Montgomery, Nancy Padian&lt;/p&gt;

Background

&lt;p xmlns:xs="http://www.w3.org/2001/XMLSchema" xmlns:fn="http://www.w3.org/2005/xpath-functions" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:util="http://dtd.nlm.nih.gov/xsl/util" xmlns:fo="http://www.w3.org/1999/XSL/Format" xmlns:mml="http://www.w3.org/1998/Math/MathML"&gt;We evaluated the effectiveness of the Ortho All-Flex Diaphragm, lubricant gel (Replens®) and condoms compared to condoms alone on the incidence of chlamydial and gonococcal infections in an open-label randomized controlled trial among women at risk of HIV/STI infections.&lt;/p&gt;

Methods

&lt;p xmlns:xs="http://www.w3.org/2001/XMLSchema" xmlns:fn="http://www.w3.org/2005/xpath-functions" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:util="http://dtd.nlm.nih.gov/xsl/util" xmlns:fo="http://www.w3.org/1999/XSL/Format" xmlns:mml="http://www.w3.org/1998/Math/MathML"&gt;We randomized 5045 sexually-active women at three sites in Southern Africa. Participants who tested positive for curable STIs were treated prior to enrollment as per local guidelines. Women were followed quarterly and tested for &lt;i&gt;Chlamydia trachomatis&lt;/i&gt; (CT) or &lt;i&gt;Neisseria gonorrhoeae&lt;/i&gt; (GC) infection by nucleic-acid amplification testing (Roche Amplicor®) using first-catch urine specimens. STIs detected at follow-up visits were treated. We compared the incidence of first infection after randomization between study arms in both intent-to-treat (ITT) and per-protocol populations.&lt;/p&gt;

Findings

&lt;p xmlns:xs="http://www.w3.org/2001/XMLSchema" xmlns:fn="http://www.w3.org/2005/xpath-functions" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:util="http://dtd.nlm.nih.gov/xsl/util" xmlns:fo="http://www.w3.org/1999/XSL/Format" xmlns:mml="http://www.w3.org/1998/Math/MathML"&gt;Baseline demographic, behavioral and clinical characteristics were balanced across study arms. Nearly 80% of participants were under 35 years of age. Median follow-up time was 21 months and the retention rate was over 93%. There were 471 first chlamydia infections, 247 in the intervention arm and 224 in the control arm with an overall incidence of 6.2/100 woman-years (wy) (relative hazard (RH) 1.11, 95% Confidence Interval (CI): 0.93–1.33; p = 0.25) and 192 first gonococcal infections, 95 in the intervention arm and 97 in the control arm with an overall incidence of 2.4/100wy (RH 0.98, 95%CI: 0.74–1.30; p = 0.90). Per protocol results indicated that when diaphragm adherence was defined as “always use” since the last visit, there was a significant reduction in the incidence of GC infection among women randomized to the intervention arm (RH 0.61, 95%CI: 0.41–0.91, P = 0.02).&lt;/p&gt;

Interpretation

&lt;p xmlns:xs="http://www.w3.org/2001/XMLSchema" xmlns:fn="http://www.w3.org/2005/xpath-functions" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:util="http://dtd.nlm.nih.gov/xsl/util" xmlns:fo="http://www.w3.org/1999/XSL/Format" xmlns:mml="http://www.w3.org/1998/Math/MathML"&gt;There was no difference by study arm in the rate of acquisition of CT or GC. However, our per-protocol results suggest that consistent use of the diaphragm may reduce acquisition of GC.&lt;/p&gt;

Trial Registration

&lt;p xmlns:xs="http://www.w3.org/2001/XMLSchema" xmlns:fn="http://www.w3.org/2005/xpath-functions" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:util="http://dtd.nlm.nih.gov/xsl/util" xmlns:fo="http://www.w3.org/1999/XSL/Format" xmlns:mml="http://www.w3.org/1998/Math/MathML"&gt;ClinicalTrials.gov NCT00121459 [&lt;a href="http://clinicaltrials.gov/ct2/show/NCT00121459"&gt;NCT00121459&lt;/a&gt;]&lt;/p&gt;&lt;img src="http://feeds.feedburner.com/~r/plosclinicaltrials/NewArticles/~4/434631242" height="1" width="1"/&gt;</content>
  <feedburner:origLink>http://clinicaltrials.ploshubs.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0003488</feedburner:origLink></entry>
  <entry>
    <title>African HIV/AIDS Trials Are More Likely to Report Adequate Allocation Concealment and Random Generation than North American Trials</title>
    <link rel="alternate" href="http://feeds.feedburner.com/~r/plosclinicaltrials/NewArticles/~3/434631243/info%3Adoi%2F10.1371%2Fjournal.pone.0003491" />
    <link rel="related" type="text/xml" href="http://clinicaltrials.ploshubs.org/article/fetchObjectAttachment.action?uri=info:doi/10.1371/journal.pone.0003491&amp;representation=XML" />
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    <author>
      <name>Nandi Siegfried et al.</name>
    </author>
    <id>info:doi/10.1371/journal.pone.0003491</id>
    <updated>2008-10-22T07:00:00Z</updated>
    <published>2008-10-22T07:00:00Z</published>
    <content type="html">&lt;p&gt;by Nandi Siegfried, Michael Clarke, Jimmy Volmink, Lize Van der Merwe&lt;/p&gt;

Background

&lt;p xmlns:xs="http://www.w3.org/2001/XMLSchema" xmlns:fn="http://www.w3.org/2005/xpath-functions" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:util="http://dtd.nlm.nih.gov/xsl/util" xmlns:fo="http://www.w3.org/1999/XSL/Format" xmlns:mml="http://www.w3.org/1998/Math/MathML"&gt;Adherence to good methodological quality is necessary to minimise bias in randomised conrolled trials (RCTs). Specific trial characteristics are associated with better trial quality, but no studies to date are specific to HIV/AIDS or African trials. We postulated that location may negatively impact on trial quality in regions where resources are scarce.&lt;/p&gt;

Methods

&lt;p xmlns:xs="http://www.w3.org/2001/XMLSchema" xmlns:fn="http://www.w3.org/2005/xpath-functions" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:util="http://dtd.nlm.nih.gov/xsl/util" xmlns:fo="http://www.w3.org/1999/XSL/Format" xmlns:mml="http://www.w3.org/1998/Math/MathML"&gt;1) To compare the methodological quality of all HIV/AIDS RCTs conducted in Africa with a random sample of similar trials conducted in North America; 2) To assess whether location is predictive of trial quality. We searched MEDLINE, EMBASE, CENTRAL and LILACS. Eligible trials were 1) randomized, 2) evaluations of preventive or treatment interventions for HIV/AIDS, 3) reported before 2004, and 4) conducted wholly or partly (if multi-centred) in Africa or North America. We assessed adequacy of random generation, allocation concealment and masking of assessors. Using univariate and multivariate logistic regression analyses we evaluated the association between location (Africa versus North America) and these domains.&lt;/p&gt;

Findings

&lt;p xmlns:xs="http://www.w3.org/2001/XMLSchema" xmlns:fn="http://www.w3.org/2005/xpath-functions" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:util="http://dtd.nlm.nih.gov/xsl/util" xmlns:fo="http://www.w3.org/1999/XSL/Format" xmlns:mml="http://www.w3.org/1998/Math/MathML"&gt;The African search yielded 12,815 records, from which 80 trials were identified. The North American search yielded 13,158 records from which 785 trials were identified and a random sample of 114 selected for analysis. African trials were three times more likely than North American trials to report adequate allocation concealment (OR = 3.24; 95%CI: 1.59 to 6.59; p&amp;lt;0.01) and twice as likely to report adequate generation of the sequence (OR = 2.36; 95%CI: 1.20 to 4.67; p = 0.01), after adjusting for other confounding factors. Additional significant factors positively associated with quality were an &lt;i&gt;a priori&lt;/i&gt; sample size power calculation, restricted randomization and inclusion of a flow diagram detailing attrition. We did not detect an association between location and outcome assessor masking.&lt;/p&gt;

Conclusions

&lt;p xmlns:xs="http://www.w3.org/2001/XMLSchema" xmlns:fn="http://www.w3.org/2005/xpath-functions" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:util="http://dtd.nlm.nih.gov/xsl/util" xmlns:fo="http://www.w3.org/1999/XSL/Format" xmlns:mml="http://www.w3.org/1998/Math/MathML"&gt;The higher quality of reporting of methodology in African trials is noteworthy. Most African trials are externally funded, and it is possible that stricter agency requirements when leading trials in other countries and greater experience and training of principal investigators of an international stature, may account for this difference.&lt;/p&gt;&lt;img src="http://feeds.feedburner.com/~r/plosclinicaltrials/NewArticles/~4/434631243" height="1" width="1"/&gt;</content>
  <feedburner:origLink>http://clinicaltrials.ploshubs.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0003491</feedburner:origLink></entry>
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