Adrenal InsufficiencyEarly Phase 1NCT03709381
Effect of Adrenocorticotropic Hormone on Vascular Endothelial Growth Factor Release in Children Study
A Early Phase 1 study testing Low Dose Cosyntropin (ACTH) stimulation test and High Dose Cosyntropin (ACTH) stimulation test in people with Adrenal Insufficiency and Osteopenia, Osteoporosis, run by Nationwide Children's Hospital at 1 site in United States.
Trial summary
Bone disease and adrenal suppression are two of the many side effects of steroid use in pediatrics. Evidence has shown that adrenocorticotropic hormone (ACTH) protects against the adverse bone effects of steroids in animals and in vitro models, but this has not yet been evaluated in humans. Read more about this study
- Who is it for?
- Ages 9 to 17 yearsHealthy volunteers can take part
- Conditions the study is for
- Adrenal Insufficiency, Osteopenia, Osteoporosis, Steroid Suppression of ACTH Secretion
- What is being tested?
- Low Dose Cosyntropin (ACTH) stimulation test and High Dose Cosyntropin (ACTH) stimulation test
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 10 participants
- Where
- 1 siteUnited States
- Study dates
- 1 Oct 2017to 31 Jan 2019
- Phase
- Early Phase 1
- 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 9 to 17 years
- All sexes
- Healthy volunteers accepted
- Child
Who may be able to join
- Subjects will be between the ages of 9-18 years old on the day of testing
Who cannot join
- Currently taking any medication other than over-the-counter medications (over-the-counter medications will be stopped on the day of the study)
- Steroid use within the prior six months (including IV, oral, inhaled, and intranasal steroids)
- Oral Contraceptive Pill use within the prior six months
- Any chronic medical conditions
- Pregnancy
Trial locations and contacts
1 site in 1 country.
United States1 site
Nationwide Children's Hospital
Columbus, Ohio, 43205
About this study
Official title: Effect of Adrenocorticotropic Hormone on Vascular Endothelial Growth Factor Release in Healthy Children and Adolescent
Bone disease and adrenal suppression are two of the many side effects of steroid use in pediatrics. Evidence has shown that adrenocorticotropic hormone (ACTH) protects against the adverse bone effects of steroids in animals and in vitro models, but this has not yet been evaluated in humans. The proposed mechanism in these studies is that ACTH stimulates osteoblasts in bone to release Vascular Endothelial Growth Factor (VEGF), which increases the vascularity in high risk areas of bone. This can potentially be protective against osteonecrosis and osteopenia, which can lead to bone fractures if not prevented. The VEGF release can also be used to demonstrate that an administration of exogenous ACTH occurred. This could be important in diagnosing adrenal insufficiency (AI). One of the tests to assess central AI is the low-dose ACTH stimulation test (LDAST). This test has a high rate of false positive results due to technical limitations. However, if an ACTH-stimulated VEGF level can be measured during the test as a marker of the test being done properly, it will allow for proper interpretation of the results (and identification of a false positive), which will reduce the number of patients being incorrectly diagnosed with central AI.
This study will recruit ten healthy children and adolescents, ages 9-18, to assess the effects of ACTH on VEGF levels. The investigators will measure the response of VEGF and cortisol to an administration of a low dose and high dose of cosyntropin (the synthetic ACTH analog used in this test). The hypothesis of this study is that VEGF and cortisol will both increase after administration of cosyntropin. At this time, no other studies have demonstrated that VEGF is responsive to ACTH in humans. If the hypothesis is correct, the results will have two main implications. VEGF can be used as a marker of ACTH administration during the LDAST to identify false positive tests. Secondly, this will help further research into whether ACTH can be used to protect against bone disease in high-dose steroid-treated patients. Further studies can be done to assess whether this effect will be the same in patients with AI or steroid-induced adrenal suppression.
Read the detailed description
Problem: Chronic steroid use causes a wide range of side effects, of which bone disease and adrenal suppression cause significant morbidity. Bone disease, which includes osteopenia, fractures, and osteonecrosis, is very common. In patients on chronic steroids, fractures can occur in up to 30-50%, low bone mineral density (BMD) can occur in up to 50%, and up to 40% have some degree of osteonecrosis. Another common side effect of steroid use is suppression of the HPA axis. This can cause a patient's endogenous cortisol and ACTH production to be reduced, which can take up to several months to return to baseline after discontinuing steroids. Diagnosing adrenal suppression can be difficult. Literature exists showing that ACTH can stimulate release of VEGF (in vitro and in animal in vivo studies), which can both be protective against bone disease and be used as a marker of exogenous cosyntropin administration. The primary goal of this study is to show that ACTH can increase VEGF levels in healthy humans.
Bone disease: As stated above, patients taking chronic steroids are at high risk for significant bone effects. Glucocorticoids cause osteoblast apoptosis and decreased function while simultaneously decreasing apoptosis of osteoclasts, overall resulting in decreased bone formation and higher resorption. This leads to low BMD and fractures. Osteonecrosis can also be due to glucocorticoid causing decreased angiogenesis in high risk areas of bone (i.e. the femoral head). In rabbits,one study demonstrated that ACTH use protects against osteonecrosis by stimulating osteoblasts to release VEGF, which maintains good blood flow to these high risk areas of bone. Another study demonstrated that Cushing Syndrome patients with ACTH-producing pituitary tumors had less BMD loss than those with adrenal cortisol-producing tumors. This outcome points toward ACTH being protective against osteopenia (even in a high steroid state). The mechanism for this protective effect is unclear but could be through ACTH stimulation of VEGF. It is unknown whether ACTH increases VEGF in humans and if it does the dose needed and timeframe of the response need to be determined.
Low-dose ACTH stimulation test (LDAST): There are several methods to evaluate adrenal insufficiency (AI), however the LDAST is best for diagnosing central AI and steroid-induced adrenal suppression (SIAS). The Metyrapone test is very specific, but it carries the risk of causing acute AI and requires a hospitalization to administer. The insulin tolerance test is the gold standard for diagnosing AI, but also carries the risk of causing hypoglycemia. The "standard" or high-dose (250mcg) ACTH stimulation test is a good test as well for diagnosing primary AI, but can result in false negatives that miss patients with central AI or SIAS, which can have significant morbidity (sensitivity for central AI is only 73%). Primary AI can also be diagnosed with an elevated ACTH level, but central AI and SIAS usually have a low to normal ACTH. Therefore, the LDAST test was created to help increase the rate of patients with central AI being diagnosed, with a sensitivity for central AI at 93%. However, there are several limitations to the LDAST. Cosyntropin is dispensed in 250 mcg vials, which is used for the high-dose test. and must be diluted to 1 mcg for the LDAST. The medication also runs the risk of sticking to IV tubing. Therefore, it is occasionally not truly given to the patient, which can cause a false positive result (the lack of cortisol response to ACTH is not due to AI, but due to never receiving cosyntropin). Due to these limitations, the specificity for diagnosing central AI is 90%. This can cause the interpreting physician to diagnose AI, and prescribe a hydrocortisone, when the patient did not truly have AI.
If the LDAST had a positive control to show that the cosyntropin appropriately reached the patient, it would help to allow the endocrinologist to recognize a false positive result. As stated above, VEGF is stimulated by ACTH in animals. If VEGF levels were measured with cortisol levels, and they rose above a set threshold, the interpreting physician could feel more comfortable knowing that the test was administered appropriately. For VEGF to be a good control value, it would need to have a significant rise in response to cosyntropin, and would need to rise quickly and after one dose (the LDAST lasts one hour) and be independent of the cortisol response. In the in vitro study above, steroid-treated cells had significant rise in VEGF within one hour of ACTH treatment, and VEGF stayed elevated for up to four hours. In a study looking at whether VEGF could be a diagnostic biomarker to differentiate acute stroke in adults versus stroke mimics, there was a significant elevation of VEGF at the time of stroke presentation compared to the average normal value (peak median 1700 pg/mL with interquartile range of 1500-1900; baseline median 466 with interquartile range of 392-649). The mechanism for rise in VEGF was postulated to be due to a hypoxia stimulus in this case. However, it seems that VEGF can be acutely stimulated (potentially within one hour of a stimulus) and has the ability to rise to several standard deviations above the normal median baseline value in humans.
VEGF: Vascular Endothelial Growth Factor is a cytokine glycoprotein that is responsible for angiogenesis, or the formation of new blood vessels. It can also maintain blood vessel density, thickness, and permeability, and it is vital for endothelial cell survival. VEGF is a family of cytokines, with VEGF-A being the prototype and most common. It is found in the lungs, kidneys, heart, adrenals, bone, brain, and several other organs. Within the adrenal, VEGF has been shown to be stimulated by ACTH and can be protective against atrophy in steroid use. Important in regards to this study, an animal study showed that VEGF can be stimulated by ACTH outside the adrenal glands, namely in osteoblasts in bone. Osteoblasts have an MC2R receptor that is stimulated by ACTH, leading to a rise in VEGF levels.
- Being tested
- Low Dose Cosyntropin (ACTH) stimulation test, High Dose Cosyntropin (ACTH) stimulation test
- Keywords
- steroid-induced adrenal suppression, vascular endothelial growth factor, adrenocorticotropic hormone, osteopenia
- Medical subject headings
- Adrenal Insufficiency, Bone Diseases, Metabolic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Low Dose Cosyntropin (ACTH) stimulation testDrug
Cosyntropin 1 mcg IV given to subjects at t=0
High Dose Cosyntropin (ACTH) stimulation testDrug
Cosyntropin 250 mcg IV given to subjects at t=60
| Study group | Role | What they receive |
|---|---|---|
| ACTH stim test arm | Experimental | Cosyntropin 1 mcg IV (low dose) will be given to subjects at t=0 minutes, and Cosyntropin 250 mcg (high dose) IV will be given to subjects at t=60 minutes. (All subjects were in the same arm and had the same protocol). Receives: Drug: Low Dose Cosyntropin (ACTH) stimulation test; Drug: High Dose Cosyntropin (ACTH) stimulation test |
What is being measured
The primary outcome is the main question the study is designed to answer.
Difference between VEGF levels at baseline and the peak VEGF level after low dose cosyntropin administration in healthy children and adolescents
Prior to administering Cosyntropin, a VEGF level will be obtained. 1 mcg Cosyntropin will be administered at t=0, then VEGF will be measured at 30 and 60 minutes. The investigators will run a comparison on the peak plasma VEGF level (the higher of the 30 and 60 minute level) after low dose stimulation compared to baseline VEGF levels.
Measured: From t=0 minutes to t=60 minutes (1 hour total)
Secondary outcomes (1)
Difference between VEGF levels at baseline and the peak VEGF level after high dose cosyntropin administration in healthy children and adolescents
After the 60 minute blood draw, a high dose (250 mcg) of Cosyntropin will be given. VEGF levels will be obtained every 30 minutes for another 2 hours (t=90, 120,150,180 min). The investigators will run a comparison on the peak plasma VEGF level (the highest of the 90, 120,150,180 minute levels) after high dose stimulation compared to baseline VEGF levels.
Measured: From t=60 minutes to t=180 minutes (2 hours total)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Oct 2018
- Study start1 Oct 2017
- Primary completion31 Oct 2018
- Study completion31 Jan 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Adrenal InsufficiencyStudies of the same condition, open and under way.
- More trials run by Nationwide Children's HospitalThe sponsor's other registered studies.
- 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
- Interventional
- Phase
- Early Phase 1
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- At t=0, 9 ml of blood will be collected for measurement of VEGF, ACTH, and cortisol levels. Then, 1 mcg of cosyntropin (a synthetic ACTH analog) will be administered intravenously (IV). Samples for measurement of cortisol and VEGF levels will be obtained at t=30 and 60 minutes (6 ml of blood collected at both times). After the 60 minute blood draw, 250 mcg of cosyntropin will be administered IV. At t=90, 120, 150 , and 180 minutes, samples for measurement of cortisol and VEGF levels will be obtained (6 ml of blood collected at each time).
- Masking
- None (open label)
- Enrolment
- 10 participants (actual)
Sponsor and investigators
- Lead sponsor
- Nationwide Children's Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ryan Heksch, Nationwide Children's Hospital
- Investigators
- Ryan Heksch, MD, Principal investigator, Nationwide Children's Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03709381
- Sponsor's protocol ID
- IRB17-00194
- Status last verified
- Feb 2019
- First submitted
- 2 Oct 2017
- Last updated
- 21 Feb 2019
- Results posted
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No: No plan to share IPD
Study at a glance
From the registry record, last updated by the sponsor on 21 Feb 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effect of Adrenocorticotropic Hormone on Vascular Endothelial Growth Factor Release in Healthy Children and Adolescent
- ClinicalTrials.gov ID
- NCT03709381
- Acronym / sponsor ID
- IRB17-00194
- Keywords
- steroid-induced adrenal suppression, vascular endothelial growth factor, adrenocorticotropic hormone, osteopenia
- Phase
- Early Phase 1
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 10 participants (actual)
- Lead sponsor
- Nationwide Children's HospitalUniversity, hospital or other
- Study start
- 1 Oct 2017 (actual)
- Primary completion
- 31 Oct 2018 (actual)
- Study completion
- 31 Jan 2019 (actual)
- First posted
- 17 Oct 2018 (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.
Bone disease and adrenal suppression are two of the many side effects of steroid use in pediatrics. Evidence has shown that adrenocorticotropic hormone (ACTH) protects against the adverse bone effects of steroids in animals and in vitro models, but this has not yet been evaluated in humans. The proposed mechanism in these studies is that ACTH stimulates osteoblasts in bone to release Vascular Endothelial Growth Factor (VEGF), which increases the vascularity in high risk areas of bone. This can potentially be protective against osteonecrosis and osteopenia, which can lead to bone fractures if not prevented. The VEGF release can also be used to demonstrate that an administration of exogenous ACTH occurred. This could be important in diagnosing adrenal insufficiency (AI). One of the tests to assess central AI is the low-dose ACTH stimulation test (LDAST). This test has a high rate of false positive results due to technical limitations. However, if an ACTH-stimulated VEGF level can be measured during the test as a marker of the test being done properly, it will allow for proper interpretation of the results (and identification of a false positive), which will reduce the number of patients being incorrectly diagnosed with central AI.
This study will recruit ten healthy children and adolescents, ages 9-18, to assess the effects of ACTH on VEGF levels. The investigators will measure the response of VEGF and cortisol to an administration of a low dose and high dose of cosyntropin (the synthetic ACTH analog used in this test). The hypothesis of this study is that VEGF and cortisol will both increase after administration of cosyntropin. At this time, no other studies have demonstrated that VEGF is responsive to ACTH in humans. If the hypothesis is correct, the results will have two main implications. VEGF can be used as a marker of ACTH administration during the LDAST to identify false positive tests. Secondly, this will help further research into whether ACTH can be used to protect against bone disease in high-dose steroid-treated patients. Further studies can be done to assess whether this effect will be the same in patients with AI or steroid-induced adrenal suppression.
Detailed description
Problem: Chronic steroid use causes a wide range of side effects, of which bone disease and adrenal suppression cause significant morbidity. Bone disease, which includes osteopenia, fractures, and osteonecrosis, is very common. In patients on chronic steroids, fractures can occur in up to 30-50%, low bone mineral density (BMD) can occur in up to 50%, and up to 40% have some degree of osteonecrosis. Another common side effect of steroid use is suppression of the HPA axis. This can cause a patient's endogenous cortisol and ACTH production to be reduced, which can take up to several months to return to baseline after discontinuing steroids. Diagnosing adrenal suppression can be difficult. Literature exists showing that ACTH can stimulate release of VEGF (in vitro and in animal in vivo studies), which can both be protective against bone disease and be used as a marker of exogenous cosyntropin administration. The primary goal of this study is to show that ACTH can increase VEGF levels in healthy humans.
Bone disease: As stated above, patients taking chronic steroids are at high risk for significant bone effects. Glucocorticoids cause osteoblast apoptosis and decreased function while simultaneously decreasing apoptosis of osteoclasts, overall resulting in decreased bone formation and higher resorption. This leads to low BMD and fractures. Osteonecrosis can also be due to glucocorticoid causing decreased angiogenesis in high risk areas of bone (i.e. the femoral head). In rabbits,one study demonstrated that ACTH use protects against osteonecrosis by stimulating osteoblasts to release VEGF, which maintains good blood flow to these high risk areas of bone. Another study demonstrated that Cushing Syndrome patients with ACTH-producing pituitary tumors had less BMD loss than those with adrenal cortisol-producing tumors. This outcome points toward ACTH being protective against osteopenia (even in a high steroid state). The mechanism for this protective effect is unclear but could be through ACTH stimulation of VEGF. It is unknown whether ACTH increases VEGF in humans and if it does the dose needed and timeframe of the response need to be determined.
Low-dose ACTH stimulation test (LDAST): There are several methods to evaluate adrenal insufficiency (AI), however the LDAST is best for diagnosing central AI and steroid-induced adrenal suppression (SIAS). The Metyrapone test is very specific, but it carries the risk of causing acute AI and requires a hospitalization to administer. The insulin tolerance test is the gold standard for diagnosing AI, but also carries the risk of causing hypoglycemia. The "standard" or high-dose (250mcg) ACTH stimulation test is a good test as well for diagnosing primary AI, but can result in false negatives that miss patients with central AI or SIAS, which can have significant morbidity (sensitivity for central AI is only 73%). Primary AI can also be diagnosed with an elevated ACTH level, but central AI and SIAS usually have a low to normal ACTH. Therefore, the LDAST test was created to help increase the rate of patients with central AI being diagnosed, with a sensitivity for central AI at 93%. However, there are several limitations to the LDAST. Cosyntropin is dispensed in 250 mcg vials, which is used for the high-dose test. and must be diluted to 1 mcg for the LDAST. The medication also runs the risk of sticking to IV tubing. Therefore, it is occasionally not truly given to the patient, which can cause a false positive result (the lack of cortisol response to ACTH is not due to AI, but due to never receiving cosyntropin). Due to these limitations, the specificity for diagnosing central AI is 90%. This can cause the interpreting physician to diagnose AI, and prescribe a hydrocortisone, when the patient did not truly have AI.
If the LDAST had a positive control to show that the cosyntropin appropriately reached the patient, it would help to allow the endocrinologist to recognize a false positive result. As stated above, VEGF is stimulated by ACTH in animals. If VEGF levels were measured with cortisol levels, and they rose above a set threshold, the interpreting physician could feel more comfortable knowing that the test was administered appropriately. For VEGF to be a good control value, it would need to have a significant rise in response to cosyntropin, and would need to rise quickly and after one dose (the LDAST lasts one hour) and be independent of the cortisol response. In the in vitro study above, steroid-treated cells had significant rise in VEGF within one hour of ACTH treatment, and VEGF stayed elevated for up to four hours. In a study looking at whether VEGF could be a diagnostic biomarker to differentiate acute stroke in adults versus stroke mimics, there was a significant elevation of VEGF at the time of stroke presentation compared to the average normal value (peak median 1700 pg/mL with interquartile range of 1500-1900; baseline median 466 with interquartile range of 392-649). The mechanism for rise in VEGF was postulated to be due to a hypoxia stimulus in this case. However, it seems that VEGF can be acutely stimulated (potentially within one hour of a stimulus) and has the ability to rise to several standard deviations above the normal median baseline value in humans.
VEGF: Vascular Endothelial Growth Factor is a cytokine glycoprotein that is responsible for angiogenesis, or the formation of new blood vessels. It can also maintain blood vessel density, thickness, and permeability, and it is vital for endothelial cell survival. VEGF is a family of cytokines, with VEGF-A being the prototype and most common. It is found in the lungs, kidneys, heart, adrenals, bone, brain, and several other organs. Within the adrenal, VEGF has been shown to be stimulated by ACTH and can be protective against atrophy in steroid use. Important in regards to this study, an animal study showed that VEGF can be stimulated by ACTH outside the adrenal glands, namely in osteoblasts in bone. Osteoblasts have an MC2R receptor that is stimulated by ACTH, leading to a rise in VEGF levels.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- At t=0, 9 ml of blood will be collected for measurement of VEGF, ACTH, and cortisol levels. Then, 1 mcg of cosyntropin (a synthetic ACTH analog) will be administered intravenously (IV). Samples for measurement of cortisol and VEGF levels will be obtained at t=30 and 60 minutes (6 ml of blood collected at both times). After the 60 minute blood draw, 250 mcg of cosyntropin will be administered IV. At t=90, 120, 150 , and 180 minutes, samples for measurement of cortisol and VEGF levels will be obtained (6 ml of blood collected at each time).
| Arm | Type | Receives |
|---|---|---|
| ACTH stim test arm | Experimental | Drug: Low Dose Cosyntropin (ACTH) stimulation test, Drug: High Dose Cosyntropin (ACTH) stimulation testCosyntropin 1 mcg IV (low dose) will be given to subjects at t=0 minutes, and Cosyntropin 250 mcg (high dose) IV will be given to subjects at t=60 minutes. (All subjects were in the same arm and had the same protocol). |
Who may qualify
- Ages
- 9 to 17 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child
Key inclusion criteria (1 listed)
- Subjects will be between the ages of 9-18 years old on the day of testing
Key exclusion criteria (5 listed)
- Currently taking any medication other than over-the-counter medications (over-the-counter medications will be stopped on the day of the study)
- Steroid use within the prior six months (including IV, oral, inhaled, and intranasal steroids)
- Oral Contraceptive Pill use within the prior six months
- Any chronic medical conditions
- Pregnancy
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 |
|---|---|---|
| Low Dose Cosyntropin (ACTH) stimulation testCosyntropin 1 mcg IV given to subjects at t=0 | Drug | ACTH stim test arm |
| High Dose Cosyntropin (ACTH) stimulation testCosyntropin 250 mcg IV given to subjects at t=60 | Drug | ACTH stim test arm |
Primary outcome
Difference between VEGF levels at baseline and the peak VEGF level after low dose cosyntropin administration in healthy children and adolescents
Time frame: From t=0 minutes to t=60 minutes (1 hour total)
Prior to administering Cosyntropin, a VEGF level will be obtained. 1 mcg Cosyntropin will be administered at t=0, then VEGF will be measured at 30 and 60 minutes. The investigators will run a comparison on the peak plasma VEGF level (the higher of the 30 and 60 minute level) after low dose stimulation compared to baseline VEGF levels.
1 secondary outcome
Difference between VEGF levels at baseline and the peak VEGF level after high dose cosyntropin administration in healthy children and adolescents
Time frame: From t=60 minutes to t=180 minutes (2 hours total)
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 21 Feb 2019.
- Individual participant dataSharing planned: No. No plan to share IPD
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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.
Ryan Heksch, MD principal investigator
Nationwide Children's Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Early Phase 1 study testing Low Dose Cosyntropin (ACTH) stimulation test and High Dose Cosyntropin (ACTH) stimulation test in people with Adrenal Insufficiency and Osteopenia, Osteoporosis, run by Nationwide Children's Hospital at 1 site in United States.
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 1 inclusion and 5 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 21 Feb 2019. 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 States. 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.
What does this phase mean?
Early Phase 1 (sometimes called Phase 0) studies give a very small amount of a treatment to a few people, mainly to see how the body handles it.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
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?
Difference between VEGF levels at baseline and the peak VEGF level after low dose cosyntropin administration in healthy children and adolescents (time frame: From t=0 minutes to t=60 minutes (1 hour total)). 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 21 Feb 2019.