This software is designed to process a subset of trial registry data from ClinicalTrials.gov that are subject to FDAAA 2017, i.e. which come with a legal obligation to report results. Such trials are known as ACTs (Applicable Clinical Trials) or pACTs (probable ACTS).
This subset is displayed in a website that makes tracking and reporting easier.
Operational overview:
- Python script
load_data.py:
- downloads a zip clinical trials registry data from ClinicalTrials.gov
- converts the XML to JSON
- uploads it to BigQuery
- runs SQL to transform it to tabular format including fields to indentify ACTs and their lateness
- downloads SQL as a CSV file
- Django management command
process_data:
- imports CSV file into Django models
- precomputes aggregate statistics and turns these into rankings
- handles other metadata (in particular, hiding trials that are no longer ACTs)
- directly scrapes the website for metadata not in the zip (specifically, trials which have been submitted but are under a QA process).
These two commands are run daily via a fab script, and the results
loaded into a staging database / website.
A separate command copies new data from staging to production (following moderation).
Much complex logic has been expressed in SQL, which makes it hard to read and test. This is a legacy of splitting the development between academics with the domain expertise (and who could use SQL to prototype) and software engineers. Now the project has been running for a while and new development interations are less frequent, a useful project would be as much of this logic to Python.
Similarly, the only reason step (1) exists is to create a CSV which can be imported to the database. That CSV is useful in its own right for QA by our academics, but the XML and JSON artefacts are just intermediate formats that could legitimately be dropped in a refactored solution (and the CSV could be generated directly from the database).
The historic reason for the XML -> JSON route is because BigQuery includes a number of useful JSON functions which can be manipulated by people competent in SQL. At the time of writing, there is an open issue with some ideas about refactoring this process.
There is a simple system to allow non-technical users to generate pages using markdown. It is documented here
Install these Python development packages before you begin. For example, on a Debian-based system:
apt install python3
Using Python 3, create and enter a virtualenv, as described here. For example:
python3 -m venv venv
. venv/bin/activate
Install required Python packages.
pip install pip-tools
pip-sync
Set environment variables required (edit environment and then run source environment).
Checkout the respository.
cd ..
git clone [email protected]:ebmdatalab/clinicaltrials-act-tracker.git
cd -
Run the application.
cd clinicaltrials
./manage.py runserver
There are a few tests.
coverage run --source='.' manage.py test
Make a coverage report:
coverage html -d /tmp/coverage_html
NOTE This section is out of date - please see #245 for work-in-progress information
We use fabric to deploy over SSH to a pet server. Deploy with
fab deploy:staging
Or
fab deploy:live
The code and data are updated via git from the master branch of their repositories.
The configuration is in fabfile.py and the deploy directory.
When setting up a new server, put environment settings live in
/etc/profile.d/fdaaa.sh.
Updating data takes around 2 hours. To do it manually, first run (from your local sandbox):
fab update:staging
This downloads and processes the data and puts it on the staging site.
It is launched as a background process using dtach. If you're happy
with this, copy data across to the live database (warning: overwrites
existing data!) with:
fab update:live
The target server
requires dtach (apt-get install dtach) to be installed by any users who
might run fabric scripts, e.g. you (the developer) and the ebmbot
user (see below)fa