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.
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.
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.
- Conditions
- Isotretinoin Adverse Reaction, Covid19
- 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 group | Role | What they receive |
|---|---|---|
| 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 |
What is being measured
The primary outcome is the main question the study is designed to answer.
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)
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.
- First posted11 Dec 2020
- Study start15 Jan 2021
- Primary completion15 Sep 2021
- Study completion15 Sep 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Isotretinoin Adverse ReactionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- University of Aberdeen
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
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.
Study at a glance
From the registry record, last updated by the sponsor on 31 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Does Oral Isotretinoin Increase the Risk of Developing Infection With and Complications From Covid-19, Compared to an Age-matched Background Population
- ClinicalTrials.gov ID
- NCT04663906
- Acronym / sponsor ID
- 1/095/20
- Conditions
- Isotretinoin Adverse Reaction, Covid19
- Keywords
- isotretinoin, Covid19, coronavirus, covid-19
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 148 participants (actual)
- Lead sponsor
- University of AberdeenUniversity, hospital or other
- Study start
- 15 Jan 2021 (actual)
- Primary completion
- 15 Sep 2021 (actual)
- Study completion
- 15 Sep 2021 (actual)
- First posted
- 11 Dec 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Observational model
- Case-control
- Time perspective
- Retrospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| 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 |
Who may qualify
- Ages
- 16 to 40 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- 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.
Key inclusion criteria (2 listed)
- 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).
Key exclusion criteria (2 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Primary Outcome
Time frame: March - October 2020
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.
1 secondary outcome
Secondary Outcome
Time frame: March - October 2020
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 Aug 2026.
- Individual participant dataSharing planned: No. Patient data will be reviewed bu study team only.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
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.