Addison DiseaseNCT05515055
Does Relative Hypoglycaemia &/or Sleep Disturbance Contribute to the Lethargy Observed in Addison's Disease
An observational study of Addison Disease, run by The Leeds Teaching Hospitals NHS Trust at 1 site in United Kingdom.
Trial summary
Addison's disease is a condition that leads to a reduction in production of steroid hormones from the adrenal glands. These hormones, particularly cortisol have many important roles in the body, one of which is increasing blood sugar. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Addison Disease
- What is being tested?
- Blood test
- How many people
- 30 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- 7 Apr 2022to 31 Dec 2024
- 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 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Importantly healthy people will be recruited who do not suffer from either Addison's disease or diabetes and will undergo the same process as detailed above to act as a healthy control group. The same exclusion criteria will apply to these participants. There are a number of people (termed controls) who have helped the research team with previous studies who will be invited to participate. These controls will be matched to a participant who suffers from Addison's disease/Addison's disease and type 1 diabetes by age, sex and a measure of height and weight termed body mass index (BMI) It is important that the two groups contain a similar population (other than suffering from Addison's disease) so that results are robust and bias is avoided.
Who may be able to join
- Aged >18 years
- Known to have Addison's disease with or without type 1 diabetes
- They are able to provide valid written consent
Who cannot join
- Having significant kidney disease
- Having active cancer, other than localised/non-aggressive skin cancer
- Being unable to provide valid written consent
- Are deemed to be inappropriate to be enrolled in the study by senior members of the research team. This may involve things such as the patient being very frail and struggles to get to and from the hospital, would have problems using the equipment due to significant visual problems or problems with hands or are known to have significant problems with low blood sugars (in those with diabetes) and already take measures to prevent this. Other exclusions may be made at the discretion of the senior investigators
Trial locations and contacts
1 site in 1 country.
United Kingdom1 site, 1 recruiting
- Recruiting
The Leeds Teaching Hospital NHS Trust
Leeds, LS9 7TF
Robert Murray, MB;BS BSc MD FRCP, 01132064578, robert.murray@leedsth.nhs.uk
About this study
Addison's disease is a condition that leads to a reduction in production of steroid hormones from the adrenal glands. These hormones, particularly cortisol have many important roles in the body, one of which is increasing blood sugar. These steroids will be replaced with tablets but fails to mimic the normal increase in natural cortisol levels which increase from around 2am in the early morning. Furthermore, steroid tablets have been associated with stopping patients from going to sleep.
Patients with Addison's disease on treatment still complain of excessive fatigue and have an increased risk of death from blood vessel diseases. Some case reports have shown some patients with Addison's disease to have low blood sugars overnight.
Read more
To investigate the possible causes of fatigue in Addison's disease by examining sugar levels and sleep patterns of our patients. Blood clotting will also be looked at as a potential mechanism for the unexplained increase in blood vessel diseases. To examine sugar levels a small probe will be attached to the upper arm which the patients will wear for 14 days to measure blood glucose very regularly and is painless. Additionally the patients will wear a watch that monitors sleep, movement, and light. A single blood sample will be taken to measure vascular risk markers and how the blood clots.
After wearing the monitors the subjects will complete questionnaires assessing quality of life. Healthy individuals will be recruited to undergo the same monitoring to act as a control group.
The data data obtained between Addison's disease and healthy subjects will be compared.
The scores from the questionnaires will be compared to the glucose and sleep readings to ascertain if there is a link between low blood sugars or sleep disturbance and their quality of life to determine if any physical abnormalities translate in to the poor quality of life.
Read the detailed description
Patients with primary adrenal insufficiency (PAI) have impaired subjective health status (1, 2) and excess mortality (3, 4). Cardiovascular disease is the greatest contributor towards the excess mortality (3). How current glucocorticoid replacement translates into these adverse sequelea is not understood. Excess and inadequate glucocorticoid replacement likely both contribute. Endogenous cortisol levels rapidly increase from 2am, peaking before waking, and thereafter fall through the day to a nadir around midnight. Hydrocortisone is the preferred glucocorticoid used for replacement therapy in PAI. Current glucocorticoid replacement regimens try to mimic the normal diurnal cortisol rhythm (5). The most commonly used regimens involve use of hydrocortisone (bio-identical to cortisol) administered three times per day (6). As cortisol levels are highest in the morning and fall through the day, a larger dose of hydrocortisone is given on waking with small doses thereafter. It is important in the timing of these doses that there is overlap to avoid periods of cortisol insufficiency. Although regimens aim to replicate the daytime cortisol profile, they cannot currently provide replacement in the early morning hours (2am-7am). This leads to a period of glucocorticoid insufficiency during sleep. Studies using continuous subcutaneous infusion (CSII) of hydrocortisone deliver hydrocortisone in a manner that mimics the normal diurnal rhythm of cortisol, including the period between 2am and waking. Hydrocortisone delivered by CSII has been associated with improvements in well-being in patients with PAI (7), though have not been used in an adequate number of patients for long enough duration to assess the impact on the excess mortality.
Insulin sensitivity is greatest between 2am-4am consequent on the diurnal rhythm of insulin counter-regulatory hormones. Consequently type I diabetic patients are at greatest risk of hypoglycaemia at this time. Glucocorticoid insufficiency increases glucose oxidation and decreases glucose production translating to increased insulin sensitivity. PAI is associated with hypoglycaemic events, though generally in children rather than adults. Using continuous glucose monitoring (CGM) a single case report (8) and a small series identified two patients with nocturnal hypoglycaemia (9). The series did not contain a control group and therefore was unable to determine if nocturnal glucose levels were lower in the patients compared with the normal population.
Furthermore, glucocorticoids have been associated with disruption of sleep, particularly difficulties getting to sleep (10). Therefore taking of replacement hydrocortisone after 6pm in the evening is avoided so that the majority of the hydrocortisone will have been metabolised before the patients retires to sleep. There are however marked differences in the timing of doses of hydrocortisone with patients often taking their doses around other life commitments, or when they are most likely to remember (i.e. first thing in the morning and last thing at night). A significant proportion of patients therefore take their last dose of steroids in the late evening or immediately prior to trying to sleep (6). This can lead hydrocortisone being taken later than prescribed and potentially impacting on sleep. However, as the dose of replacement hydrocortisone is low when given in the evening it is not known if sleep is adversely affected in contrast to that observed with higher therapeutic doses of glucocorticoids?
Finally, much of the excess mortality of patients with primary adrenal insufficiency is reported to relate to vascular disease (3). Vascular risk factors are variably reported to be increased in PAI (11). However, the mechanism by which the excess vascular disease occurs remains incompletely understood.
- Conditions
- Addison Disease
- Being tested
- Blood test
- Medical subject headings
- Addison Disease
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Blood testOther
1 blood sample extra to standard of care is taken
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of low blood sugars events overnight in patients with Addison's disease will be measured to determine if there is an increased number of low blood sugars events overnight in patients who suffer from Addison's disease.
Measured: 3 months
Secondary outcomes (4)
Is the mean blood sugars of patient's with Addison's disease lower than in healthy subjects and Is there greater variation in blood sugar in patients with Addison's disease?
Measured: 3 months
Does having low blood sugars contribute to the impaired quality of life of patients with Addison's disease and does sleep disturbance contribute to the impaired quality of life of patients with Addison's disease?
Measured: 3 months
To examine vascular risk factors, particularly abnormalities of clot formation and degradation, that may contribute to the reported excess mortality of patients with PAI.
Measured: 3 months
Does physiological steroid replacement lead to disturbance of normal sleep patterns?
Measured: 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Aug 2022
- Study start7 Apr 2022
- Primary completion31 Dec 2024 (estimated)
- Study completion31 Dec 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Addison DiseaseStudies 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
- Cohort
- Time perspective
- Prospective
- Enrolment
- 30 participants (estimated)
Sponsor and investigators
- Lead sponsor
- The Leeds Teaching Hospitals NHS Trust
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05515055
- Sponsor's protocol ID
- ED22/147142
- Status last verified
- Jul 2023
- First submitted
- 19 May 2022
- Last updated
- 17 Jul 2023
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 17 Jul 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Does Relative Hypoglycaemia &/or Sleep Disturbance Contribute to the Lethargy Observed in Addison's Disease
- ClinicalTrials.gov ID
- NCT05515055
- Acronym / sponsor ID
- ED22/147142
- Conditions
- Addison Disease
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 30 participants (estimated)
- Lead sponsor
- The Leeds Teaching Hospitals NHS TrustUniversity, hospital or other
- Study start
- 7 Apr 2022 (actual)
- Primary completion
- 31 Dec 2024 (estimated)
- Study completion
- 31 Dec 2024 (estimated)
- First posted
- 25 Aug 2022 (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.
Addison's disease is a condition that leads to a reduction in production of steroid hormones from the adrenal glands. These hormones, particularly cortisol have many important roles in the body, one of which is increasing blood sugar. These steroids will be replaced with tablets but fails to mimic the normal increase in natural cortisol levels which increase from around 2am in the early morning. Furthermore, steroid tablets have been associated with stopping patients from going to sleep.
Patients with Addison's disease on treatment still complain of excessive fatigue and have an increased risk of death from blood vessel diseases. Some case reports have shown some patients with Addison's disease to have low blood sugars overnight.
To investigate the possible causes of fatigue in Addison's disease by examining sugar levels and sleep patterns of our patients. Blood clotting will also be looked at as a potential mechanism for the unexplained increase in blood vessel diseases. To examine sugar levels a small probe will be attached to the upper arm which the patients will wear for 14 days to measure blood glucose very regularly and is painless. Additionally the patients will wear a watch that monitors sleep, movement, and light. A single blood sample will be taken to measure vascular risk markers and how the blood clots.
After wearing the monitors the subjects will complete questionnaires assessing quality of life. Healthy individuals will be recruited to undergo the same monitoring to act as a control group.
The data data obtained between Addison's disease and healthy subjects will be compared.
The scores from the questionnaires will be compared to the glucose and sleep readings to ascertain if there is a link between low blood sugars or sleep disturbance and their quality of life to determine if any physical abnormalities translate in to the poor quality of life.
Detailed description
Patients with primary adrenal insufficiency (PAI) have impaired subjective health status (1, 2) and excess mortality (3, 4). Cardiovascular disease is the greatest contributor towards the excess mortality (3). How current glucocorticoid replacement translates into these adverse sequelea is not understood. Excess and inadequate glucocorticoid replacement likely both contribute. Endogenous cortisol levels rapidly increase from 2am, peaking before waking, and thereafter fall through the day to a nadir around midnight. Hydrocortisone is the preferred glucocorticoid used for replacement therapy in PAI. Current glucocorticoid replacement regimens try to mimic the normal diurnal cortisol rhythm (5). The most commonly used regimens involve use of hydrocortisone (bio-identical to cortisol) administered three times per day (6). As cortisol levels are highest in the morning and fall through the day, a larger dose of hydrocortisone is given on waking with small doses thereafter. It is important in the timing of these doses that there is overlap to avoid periods of cortisol insufficiency. Although regimens aim to replicate the daytime cortisol profile, they cannot currently provide replacement in the early morning hours (2am-7am). This leads to a period of glucocorticoid insufficiency during sleep. Studies using continuous subcutaneous infusion (CSII) of hydrocortisone deliver hydrocortisone in a manner that mimics the normal diurnal rhythm of cortisol, including the period between 2am and waking. Hydrocortisone delivered by CSII has been associated with improvements in well-being in patients with PAI (7), though have not been used in an adequate number of patients for long enough duration to assess the impact on the excess mortality.
Insulin sensitivity is greatest between 2am-4am consequent on the diurnal rhythm of insulin counter-regulatory hormones. Consequently type I diabetic patients are at greatest risk of hypoglycaemia at this time. Glucocorticoid insufficiency increases glucose oxidation and decreases glucose production translating to increased insulin sensitivity. PAI is associated with hypoglycaemic events, though generally in children rather than adults. Using continuous glucose monitoring (CGM) a single case report (8) and a small series identified two patients with nocturnal hypoglycaemia (9). The series did not contain a control group and therefore was unable to determine if nocturnal glucose levels were lower in the patients compared with the normal population.
Furthermore, glucocorticoids have been associated with disruption of sleep, particularly difficulties getting to sleep (10). Therefore taking of replacement hydrocortisone after 6pm in the evening is avoided so that the majority of the hydrocortisone will have been metabolised before the patients retires to sleep. There are however marked differences in the timing of doses of hydrocortisone with patients often taking their doses around other life commitments, or when they are most likely to remember (i.e. first thing in the morning and last thing at night). A significant proportion of patients therefore take their last dose of steroids in the late evening or immediately prior to trying to sleep (6). This can lead hydrocortisone being taken later than prescribed and potentially impacting on sleep. However, as the dose of replacement hydrocortisone is low when given in the evening it is not known if sleep is adversely affected in contrast to that observed with higher therapeutic doses of glucocorticoids?
Finally, much of the excess mortality of patients with primary adrenal insufficiency is reported to relate to vascular disease (3). Vascular risk factors are variably reported to be increased in PAI (11). However, the mechanism by which the excess vascular disease occurs remains incompletely understood.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Importantly healthy people will be recruited who do not suffer from either Addison's disease or diabetes and will undergo the same process as detailed above to act as a healthy control group. The same exclusion criteria will apply to these participants. There are a number of people (termed controls) who have helped the research team with previous studies who will be invited to participate. These controls will be matched to a participant who suffers from Addison's disease/Addison's disease and type 1 diabetes by age, sex and a measure of height and weight termed body mass index (BMI) It is important that the two groups contain a similar population (other than suffering from Addison's disease) so that results are robust and bias is avoided.
Key inclusion criteria (3 listed)
- Aged >18 years
- Known to have Addison's disease with or without type 1 diabetes
- They are able to provide valid written consent
Key exclusion criteria (4 listed)
- Having significant kidney disease
- Having active cancer, other than localised/non-aggressive skin cancer
- Being unable to provide valid written consent
- Are deemed to be inappropriate to be enrolled in the study by senior members of the research team. This may involve things such as the patient being very frail and struggles to get to and from the hospital, would have problems using the equipment due to significant visual problems or problems with hands or are known to have significant problems with low blood sugars (in those with diabetes) and already take measures to prevent this. Other exclusions may be made at the discretion of the senior investigators
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Blood test1 blood sample extra to standard of care is taken | Other | – |
Primary outcome
Number of low blood sugars events overnight in patients with Addison's disease will be measured to determine if there is an increased number of low blood sugars events overnight in patients who suffer from Addison's disease.
Time frame: 3 months
4 secondary outcomes
Is the mean blood sugars of patient's with Addison's disease lower than in healthy subjects and Is there greater variation in blood sugar in patients with Addison's disease?
Time frame: 3 months
Does having low blood sugars contribute to the impaired quality of life of patients with Addison's disease and does sleep disturbance contribute to the impaired quality of life of patients with Addison's disease?
Time frame: 3 months
To examine vascular risk factors, particularly abnormalities of clot formation and degradation, that may contribute to the reported excess mortality of patients with PAI.
Time frame: 3 months
Does physiological steroid replacement lead to disturbance of normal sleep patterns?
Time frame: 3 months
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Jul 2023.
- Individual participant dataSharing planned: No
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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.
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 Addison Disease, run by The Leeds Teaching Hospitals NHS Trust 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 3 inclusion and 4 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: status not confirmed, as of the sponsor's last update on 17 Jul 2023. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of low blood sugars events overnight in patients with Addison's disease will be measured to determine if there is an increased number of low blood sugars events overnight in patients who suffer from Addison's disease. (time frame: 3 months). 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 17 Jul 2023.