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Isotretinoin Adverse ReactionNCT04663906

Oral Isotretinoin and Covid-19 Infection

An observational study of Isotretinoin Adverse Reaction and Covid19, run by University of Aberdeen at 1 site in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

There is a theoretical risk that the nasal mucosal dryness caused by oral retinoid medications may increase risk of infection with Covid-19. Isotretinoin arrests the cell cycle of mucus secreting cells in the nasal cavity, and cilia and mucus are both believed to have roles in defence against infection and immunity. Read more about this study

Who is it for?
Ages 16 to 40 yearsHealthy volunteers can take part
Conditions the study is for
Isotretinoin Adverse Reaction, Covid19
Type of treatment
Pill or oral medicine
How many people
148 participants
Where
1 siteUnited Kingdom
Study dates
15 Jan 2021to 15 Sep 2021
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 16 to 40 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Study population: 148 patients taking isotretinoin aged 16-40 extracted from a clinical departmental database. Rates per 100000 were compared with the background age-matched local (NHS Grampian / Moray) population n=189633 people. The numbers in each population were finally determined when the database was interrogated and details were obtained from Health Intelligence, neither of which could happen prior to approvals.

Who may be able to join

  • Test: prescribed oral isotretinoin in NHS Grampian age 16-40years inclusive, between March-Oct 2020
  • Background control population: residing in NHS Grampian including Moray catchment, age 16-40years, (this was found to be n=189633 people).

Who cannot join

  • Test population: not prescribed oral isotretinoin in NHS grampian, outwith age range 16-40years or treatment range March-October 2020.
  • Background control population: age outwith 16-40years, not resident in NHS Grampian / Moray catchment.

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • Aberdeen Royal Infirmary

    Aberdeen

Other trials in United Kingdom

About this study

Official title: Does Oral Isotretinoin Increase the Risk of Developing Infection With and Complications From Covid-19, Compared to an Age-matched Background Population

There is a theoretical risk that the nasal mucosal dryness caused by oral retinoid medications may increase risk of infection with Covid-19. Isotretinoin arrests the cell cycle of mucus secreting cells in the nasal cavity, and cilia and mucus are both believed to have roles in defence against infection and immunity. Hence it was postulated at the start of the pandemic that isotretinoin may increase the likelihood of contracting a disease spread by droplet or aerosol particles.

The investigators planned to compare rates of infection and deterioration between our group of patients taking isotretinoin, aged 16-40years, and the local (NHS Grampian / Moray) age-matched population.

Read the detailed description

Isotretinoin is a drug used commonly in dermatology, usually for management of acne and occasionally for management of other dermatological diseases. The most common side effect of oral isotretinoin is mucocutaneous dryness, which can lead to nasal dryness and crusting. Isotretinoin is derived from vitamin A and produces this side effect by arresting the cell cycle of mucus secreting cells in the nasal cavity. The mucus usually secreted moisturises the nasal cavity and provides a protective, lubricating layer overlying the cilia.

Cilia and nasal mucous are both believed to have roles in defence against infection and immunity. Hence it was postulated at the start of the pandemic that the effect this medication has on the nasal environment may increase the likelihood of contracting a disease spread by droplet or aerosol particles, such as Covid-19.

In March 2020 the investigators established a departmental database of our patients on oral retinoid medications in order to track those currently receiving treatment. The database includes people taking isotretinoin, alitretinoin and acitretin. The greatest number of patients in this database are in the isotretinoin group and patients taking isotretinoin tend to be a relatively young and fit population. Acitretin on the other hand is often used in an older population who may have other underlying disease comorbidities. There were only a very small number of patients taking alitretinoin in the database.

In order to limit confounding variables and provide as clear a result as possible, it was decided to limit this study to comparing the group of patients taking isotretinoin, aged 16-40years, and compare their rates per 100000 of infection and deterioration with the age-matched local population from NHS Grampian \& Moray catchment.

This study would examine the electronic patient record of patients aged 16-40years, taking isotretinoin between March and October 2020 and compare their rates of Covid-19 infection, hospitalisation and complications with the rates of the local age-matched background population. In initial protocols, prior to data being obtained, persons taking isotretinoin in the time period were to be excluded from the background population - unfortunately on obtaining the data, which could only be achieved after this protocol was originally written, it was not possible to exclude those taking isotretinoin, therefore the isotretinoin population's rates were to be compared against the age-matched local population as a whole.

As Covid-19 is a new disease, the existing research literature on this specific topic is extremely limited, and so far this study would be the first in this area.

The electronic patient record of patients aged 16-40years taking isotretinoin between March and October 2020 will be accessed and the following will be recorded:

  • Covid-19 testing while on or within 4 weeks after treatment
  • Positive Covid-19 test while on or within 4 weeks after treatment
  • Hospitalisation with Covid-19 while on or within 4 weeks after treatment
  • ICU admission while on or within 4 weeks of treatment
  • Death directly attributed to Covid-19 while on or within 4 weeks of treatment.

Rates per 100000 would be calculated.

The data held in the database is identifiable and held on the NHS Grampian secure server.

Once the details above are filled in each case will be anonymised with a case number. A key linking this back to the CHI will be kept on the NHS Grampian secure server.

Further data analysis will be completed using the anonymised data.

Details of an age matched local population can be obtained from Health Intelligence pending R\&D approval of this study.

The University of Aberdeen department of medical statistics have already been consulted about this project and are willing to offer their help with data analysis. Once statistical analysis has been decided upon the investigators will update the protocol or submit the details as an amendment, before analysis takes place.

Keywords
isotretinoin, Covid19, coronavirus, covid-19
Medical subject headings
COVID-19, Coronavirus Infections

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT04663906
Study groupRoleWhat they receive
IsotretinoinTest population, prescribed oral isotretinoin between March and October 2020.
ControlBackground age-matched local population (NHS Grampian including Moray) during March to October 2020

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Primary Outcome

    Did patients taking isotretinoin have a greater risk of infection with Covid-19 compared to the age-matched local population.

    Rates per 100000 of covid testing and positive results indicating covid infection were compared between a cohort taking isotretinoin, and the age matched local (NHS Grampian \&Moray) population.

    Measured: March - October 2020

Secondary outcomes (1)
  1. Secondary Outcome

    Did patients taking isotretinoin have a greater risk of hospitalisation related to Covid-19, ICU admission, or death from Covid-19, compared to the age-matched background population.

    Rates per 100000 of covid related hospital admission, ICU admission and death were compared between a cohort taking isotretinoin, and the age matched local (NHS Grampian and Moray) population.

    Measured: March - October 2020

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Dec 2020
  2. Study start15 Jan 2021
  3. Primary completion15 Sep 2021
  4. Study completion15 Sep 2021

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Retrospective
Enrolment
148 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04663906
Sponsor's protocol ID
1/095/20
Status last verified
Dec 2020
First submitted
10 Dec 2020
Last updated
31 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Patient data will be reviewed bu study team only.

Questions about this trial

What is this clinical trial studying?

An observational study of Isotretinoin Adverse Reaction and Covid19, run by University of Aberdeen at 1 site in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 31 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Primary Outcome (time frame: March - October 2020). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Aug 2026.

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