Welcome! Another blog appears at last …
One of the dental trials I am currently working on is being carried out in several countries (we are in the process of getting it off the ground here in the UK). The trial is a comparison of different treatments for decay in children’s teeth and their outcomes.
I've been challenged by a couple of my fellow researchers to justify one of the particular aspects of trial beaurocracy - Clinical Trial Registration - that I have suggested is important. Although widespread in medical trials (especially for trials of medicinal products), it's really not really the norm yet to register dental trials.
Often, the bureaucracy associated with setting up and running clinical trials (although necessary) is often seen as a hindrance, especially as it’s a bit of a ‘one size fits all’. So no allowance is made for trials comparing two ‘standard’ non-dangerous treatments as opposed to those testing a ‘new’ treatment with unknown and potentially damaging side effects.
However, rather than being a hindrance, Trial Registration is actually one of the things that is a help. It's an international move that has been encouraged from a number of fronts. The idea behind obligatory registration of all clinical trials (drugs, devices, surgical procedures, dental treatments etc etc) is to create a publicly available database of trials being carried out. But really - why bother? Well, I'm going to have a stab at that justification to my co-researchers now...
I've been challenged by a couple of my fellow researchers to justify one of the particular aspects of trial beaurocracy - Clinical Trial Registration - that I have suggested is important. Although widespread in medical trials (especially for trials of medicinal products), it's really not really the norm yet to register dental trials.
Often, the bureaucracy associated with setting up and running clinical trials (although necessary) is often seen as a hindrance, especially as it’s a bit of a ‘one size fits all’. So no allowance is made for trials comparing two ‘standard’ non-dangerous treatments as opposed to those testing a ‘new’ treatment with unknown and potentially damaging side effects.
However, rather than being a hindrance, Trial Registration is actually one of the things that is a help. It's an international move that has been encouraged from a number of fronts. The idea behind obligatory registration of all clinical trials (drugs, devices, surgical procedures, dental treatments etc etc) is to create a publicly available database of trials being carried out. But really - why bother? Well, I'm going to have a stab at that justification to my co-researchers now...
Publishing
Future proofing
As we
all know, trials take an absolute age to set up, carry out well, follow up and
then publish the findings of. Standards in publication in dental journals
are improving (reporting guidelines such as CONSORT are slowly becoming more
widely used). Should journals that we might be expecting to publish in,
have a change in editorship or policy, and the Uniform Requirements for Manuscripts
Submitted to Biomedical Journals be adhered to, it would be wise to be
prepared.
Transparency
Registering
your trial makes it more visible and means that if someone else wants to do the
same trial or a similar trial to you, when they check on the standard clinical
trial databases before starting theirs (or when their funding body do), they
will see what you are doing and may request to join forces, improving the
generalisability of the trial. Alternatively, they may decide their work
is unnecessary (and thus avoid patients being pointlessly entered into a trial
that you are going to find the answer to anyway!). The other advantage of
visibility is that if someone is going to do a similar type of trial, they will
be aware of your expertise and can contact you to help avoid the pitfalls you
will no doubt have encountered, find out what worked well in terms of outcome
measures, patient preferences etc and maybe use similar tools to enable
comparisons between trials (something that is currently pretty poor in
Dentistry).
Overlapping publications
When the
trial registration number is attached to the end of every manuscript associated
with that trial, it means that readers will always know the data (whether it's
different datasets or similar datasets at different times), all came from the
same trial. It also makes life much easier for those of us undertaking
systematic reviews.
And last but should really be first – Patients
One of
the (perhaps future) benefits of trials being registered on a publically
accessible database is that patients can see the kind of research being carried
out in Oral Health and Dentistry. This helps raise awareness of what is
available to them or at least, what we are testing to try to improve
treatments. This can only help the informed dialogue all clinicians
should be having with patients/ public about treatment options.
If you
are peer reviewing a paper for a journal then and it’s a prospective clinical
trial, check to see if it’s been registered anywhere, and if it has, check that
the authors have stuck to their original stated aim. Also, if the journal
you are reviewing for is registered with the ICMJE, as being signed up to the
Uniform Requirements, check that they are encouraging authors to adhere to
these standards. Although it will take time, this will help to improve
the quality of the trials in dentistry and therefore ultimately the care we
provide for our patients.
There are a number of different
trials registries which are acceptable to the ICMJE including: www.anzctr.org.au,
www.clinicaltrials.gov, www.ISRCTN.org, www.umin.ac.jp/ctr/index/htm, www.trialregister.nl, https://eudract.ema.europa.eu/ and although some have a cost
attached, others don’t.
No comments:
Post a Comment