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CompletedNCT04663906Updated Aug 31, 2026

Oral Isotretinoin and Covid-19 Infection

An observational study in Isotretinoin Adverse Reaction and Covid19, sponsored by University of Aberdeen. Completed at 1 site in United Kingdom. Open to participants aged 16 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-31.

Sponsored by University of Aberdeen · Observational

Study type
Observational
Model
Case-control
Time perspective
Retrospective
Enrollment
148
Ages
16 Years to 40 Years
Sex
All
01

Study 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. 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.

02

Conditions studied

  • Isotretinoin Adverse Reaction
  • Covid19

Keywords

  • isotretinoin
  • Covid19
  • coronavirus
  • covid-19
03

In context

COVID-19

7,640 studies on the registry are indexed under COVID-19; 488 are open to participants now.

This study's enrollment of 148 is below the median of 260 across 3,135 observational studies indexed under COVID-19.

Browse COVID-19 studies →

Lead sponsor

University of Aberdeen is the lead sponsor of 170 studies on the registry; 23 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

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.

Inclusion criteria

  • 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).

Exclusion criteria

Exclusion Criteria:

  • 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.

05

Study design

Observational model
Case-control
Time perspective
Retrospective
Enrollment
148 participants (actual)
Patient registry
No

Groups and cohorts

  • Isotretinoin

    Test population, prescribed oral isotretinoin between March and October 2020.

  • Control

    Background age-matched local population (NHS Grampian including Moray) during March to October 2020

06

What researchers measure

Primary outcomes

  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.

    Time frame: March - October 2020

Secondary outcomes

  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.

    Time frame: March - October 2020

07

Study locations

1 site
  • Aberdeen Royal Infirmary
    Aberdeen, United Kingdom
08

References and documents

Individual participant data

Plan to share: No — Patient data will be reviewed bu study team only.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 31, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04663906
Lead sponsor
University of Aberdeen
Responsible party
Sponsor
First posted
Dec 11, 2020
Start date
Jan 15, 2021
Primary completion
Sep 15, 2021
Completion
Sep 15, 2021
Last update
Aug 31, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2020. You cannot join it, but the record below documents what was studied.

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