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ICPR 221 : Epidemiology and global health (HC)
HEALTH STATISTICS & DEMOGRAPHICS:
GlobalHealthReporting.org
HNPStats
OECD Statistics Page
WHO Health Statistics: Evidence and Information for Health Policy
CIA World Fact Book: Country Profiles
MEDICAL NEWS:
The Lancet Global Health Network
Harvard World Health News
Healthmap.org
DATABASES (for reports and journal articles on diseases)
Access world news
Provider: NewsBank
LexisNexis academic
Provider: LN
PAIS international
Provider: CSA
ProQuest Research Library
Provider: ProQuest
PubMed
Provider: NCBI
PubMed central
Relemed
Web of science
Provider: ISI
BASIC MEDICAL INFORMATION RESOURCES:
AccessScience @ McGraw-Hill
Healthfinder.gov
A one-stop information source to learn about disease conditions, patient education and research and patient support organizations for specific conditions. Sponsored by the Office of Disease Prevention and Health Promotion.
MedlinePlus
from the National Library of Medicine -Comprehensive site with information on drugs and supplements, medical dictionary and encyclopedia and convenient access to both consumer and professional level literature.
The Merck manual of medical information -- Home Edition
Explains diseases in simple English. Multimedia resources (animations, audio, photographs and videos) help illustrate complex subjects. Each topic has links to an audio glossary and multimedia.
CLINICAL TRIALS:
FDA
The Food and Drug Administration is responsible for the approval of all drugs, biologicals, medical devices, cosmetics and radiological products. Check out this FDA Consumer Magazine article on clinical trials and what constitutes informed consent. The FDA homepage has links to appropriate information for various target audiences. Guidance documents on good clinical practices in clinical trials are posted.
PDR.net's Clinical Trial Resource Center
Clinical Trial Portals
ClinicalTrials.gov
This is the official site from NIH for finding clinical trials from 161 countries by condition, location, sponsor, study type (interventional, observational and expanded access) and status. Resources listed on the same page are useful for understanding the process and the language used in clinical trials for a basic understanding in order to be an informed participant.
International Clinical Trials Registry Platform (ICTRP) Search Portal from WHO
- Australian New Zealand Clinical Trials Registry (ANZCTR)
- Chinese Clinical Trial Register (ChiCTR)
- ClinicalTrials.gov (U.S. NIH but contains information from 161 countries)
- Clinical Trials Registry - India (CTRI)
- German Clinical Trials Register (DRKS)
- ISRCTN.org (an international non-profit organization that seeks to create unique IDs for clinical trials)
- The Netherlands National Trial Register (NTR)
IFPMA Clinical Trials Portal
The Portal's search engine has been programmed to access relevant on-line sources of clinical trial information. These include individual pharmaceutical company sites, sites run by third parties working on behalf of these companies, pharmaceutical industry association resources, such as the US pharmaceutical industry association (PhRMA) site clinicalstudyresults.org and government sites which routinely carry details of industry trials, such as the US National Library of Medicine's http://www.clinicaltrials.gov. Other on-line clinical trial information resources, such as the European Union's planned Europharm facility, may be linked to as they become available.
European Organisation for Research and Treatment of Cancer (EORTC) Protocols Database
Originally founded as an international organisation under Belgian law in 1962 by eminent oncologists working in the main cancer research institutes of the EU countries and Switzerland.became the European Organisation for Research and Treatment of Cancer (EORTC) in 1968. The aims are to develop, conduct, coordinate, and stimulate translational and clinical research in Europe to improve the management of cancer and related problems by increasing survival but also patient quality of life.
Drug Information Portal from the National Library of Medicine
Active Trials Portals
Africa Clinical Trials Portal (ACTP)
Asia Clinical Trials Portal (ASCTP)
For on-going trials only. No historical information.
ASCTP is a comprehensive online resource for easily accessible information on malaria, HIV/AIDS, and TB clinical trials in Asia. The portal is a one-stop resource that allows users to:
- Access clinical trial information using a database of pre-licensure clinical trials of malaria, HIV/AIDS, and TB drugs, vaccines and microbicides that are currently underway in Asia.
- Obtain accurate information on clinical trial sites in Asia.
- View a continent-wide map that displays clinical trial and site information using interactive web-based mapping technology.
Citation Guides for Medicine
How to cite a clinical trial from ClinicalTrials.gov
Patrias, K. Citing medicine: the NLM style guide for authors, editors, and publishers [Internet]. 2nd ed. Wendling, DL, technical editor. Bethesda (MD): National Library of Medicine (US); 2007 [updated 2009 Jan 14; cited Year Month Day]. Available from: http://www.nlm.nih.gov/citingmedicine
How to cite a record on a clinical trials register (from WHO)
Ethical Guidelines
The Belmont Report: Ethical Principles and Guidelines for the Protection of Subjects of Human Research
Declaration of Helsinki: ethical prinicples for medical research involving human subjects.
Regulations
Progress and Deficiencies in the Registration of Clinical Trials
Details summary of Section 801 FDA Amendment Act of 2007 notes in general:
- Strengthens requirements for registration- all trials except Phase I with a US site must be registered no later than 21 days after enrollment of first participant
- Basic results reporting must be no later than 1 year after the date that the final subject was examined or received an intervention.
- For trials to establish new uses of already approved drug, reporting can be delayed up to 3 years.
MEDICINE: Moving Toward Transparency of Clinical Trials
Reporting Randomized Controlled Trials
CONSORT Website
From the website:
CONSORT, which stands for Consolidated Standards of Reporting Trials, encompasses various initiatives developed by the CONSORT Group to alleviate the problems arising from inadequate reporting of randomized controlled trials (RCTs).
The main product of CONSORT is the CONSORT Statement, which is an evidence-based, minimum set of recommendations for reporting RCTs. It offers a standard way for authors to prepare reports of trial findings, facilitating their complete and transparent reporting, and aiding their critical appraisal and interpretation.
CONSORT for Reporting RCTs in Journal and Conference Abstracts
This article explains the checklist times in CONSORT, give an example for each item and explains why and what makes a good description for each item.




