Comparison of Cortisol Pump With Standard Treatment for Congenital Adrenal Hyperplasia

Phase

Condition

Wolman Disease

Cushing's Disease

Congenital Adrenal Hyperplasia

Treatment

N/A

Clinical Study ID

NCT01859312

130121

13-CH-0121

Ages 18-99
All Genders

Study Summary

Background:

Congenital adrenal hyperplasia (CAH) is a genetic disorder of the adrenal gland. The adrenal gland is located in the abdomen and produces small amounts of hormones such as cortisol, aldosterone, and androgen. These hormones help control blood pressure, protect the body, and maintain good health, especially during development. People with CAH do not make enough cortisol and aldosterone, and make too much androgen. This can lead to serious medical problems. The standard treatment is to take pills that mimic the effects of cortisol and aldosterone. However, treatment with pills can have long-term side effects because of the higher doses needed, and may not work well for some people.
A possible new treatment for CAH is to use a pump to deliver cortisol under the skin. Similar pumps are often used to give insulin to people with diabetes. Researchers think that a cortisol pump might be able to help the body use the cortisol more effectively than taking pills. They want to compare the results of a cortisol pump and standard pill treatments for CAH.

Objectives:

To compare the effectiveness of a cortisol pump with standard cortisol pill therapy for CAH.

Eligibility:

Men and women at least 18 years of age who have CAH (see more details in Eligibility section below).

Design:

This study will involve four inpatient hospital stays at the National Institutes of Health in Bethesda, MD over 6 months (spaced 2 months apart). The first and last stays will last about 5 days. The second and third stays will last about 3 days.
Participants will be screened with a physical exam and medical history. Blood and urine samples will be collected.
At the first study visit, participants will provide regular blood and urine samples. They will also have imaging studies. These studies will look at the bones, fat, and muscles in the abdomen and pelvis.
Participants will receive a cortisol pump during the first visit. They will be shown how to use the pump. They will also learn what to do, if they need to take extra "stress dose" cortisol pills.
At the second and third visits, the cortisol dose given with the pump will be adjusted as needed. Blood and urine samples will also be collected. No imaging studies are scheduled for these visits.
The last study visit will have the same tests as the first visit. Participants will be offered the chance to continue with the pump treatment for 1 more year, or go back to their standard pill treatment.

Study type: Interventional non-randomized trial

Official title: A Pilot Study Assessing the use of Continuous Subcutaneous Hydrocortisone Infusion In the Treatment of Congenital Adrenal Hyperplasia

Estimated enrollment: 8

Study Start Date: May 2013

Estimated Study Completion Date: December 2016

Sponsoring Institute: National Institute of Child Health and Human Development

<TAB>ELIGIBILITY

Inclusion criteria

Men and women 18 years of age or older with classic congenital adrenal hyperplasia (21-Hydroxylase deficiency)
High adrenal androgens in the blood, and
One or more of the following conditions: obesity, fatty liver, risk for diabetes, low bone mass, inability to tolerate cortisol pills

Exclusion criteria

Pregnancy
Breast feeding
Use of inhaled or oral steroids for diseases other than CAH
Use of estrogen-containing birth control pills
Use of medicines that cross-react with hydrocortisone
Use of stress dose steroids for illness during the last 30 days prior to joining the study

Eligibility Criteria

Inclusion

INCLUSION CRITERIA:
Patients with known classic CAH due to 21-hydroxylase deficiency as evidenced byhormonal and genetic testing
Male or female patients 18 years or older
Females must have a negative pregnancy test initially and at all visits. Sexuallyactive females must be using a medically acceptable method of contraception.
Patients with elevated adrenal androgens (defined as 17-OHP >1200 ng/dL andandrostenedione >210 ng/dL)
One or more co-morbidities:<TAB>
Obesity [body mass index (BMI) greater than 30.0 kg/m(2)]
Fatty liver disease; assessed by AST/ALT liver enzyme ratio (AST to ALT ratio <1 (11))liver ultrasound or MRI imaging (Steatosis score as previously described)
Low insulin sensitivity; assessed by the Homeostasis Model Assessment InsulinResistance (HOMA-IR) method [HOMA-IR = insulin (micro U/ml) times glucose (mmol/L)/ 22.5]. Elevated HOMA-IR index is defined as >2.6 in adults17.
Osteopenia [bone mineral density by DEXA (at the spine, hip, or forearm) with T-scoreof -1 to -2.5) or osteoporosis (bone mineral density by DEXA (at the spine, hip, orforearm) with T-score of <-2.5] defined according to World Health Organization (WHO).
Glucocorticoid-related gastrointestinal side effects (nausea, vomiting, dyspepsia,anorexia, gastritis, peptic ulcer disease and gastric bleeding)

Exclusion

EXCLUSION CRITERIA:

Co-morbid conditions requiring daily administration of medications that induce hepaticenzymes or interfere with the metabolism of glucocorticoids
Females who are pregnant or lactating
Patients on inhaled or oral steroids given for reasons other than treatment of CAH
Women who have taken estrogen-containing oral contraceptive pills within 6 weeks ofrecruitment
Patients who required stress dose glucocorticoids for an illness within 4 weeks ofrecruitment
Patients who changed their glucocorticoid agent within 3 months of recruitment
Patients who underwent bilateral adrenalectomy
Co-morbid conditions that could interfere with the ability to comply to the protocol

Study Design

May 06, 2013

December 02, 2016

Study Description

Congenital adrenal hyperplasia (CAH) is a common genetic endocrine disorder, with 21-hydroxylase enzyme deficiency accounting for 95% of the cases. 21-hydroxylase deficiency presents with a spectrum of clinical manifestations ranging from salt-wasting and virilization of female neonates (classic CAH) to symptomatic (precocious puberty, short stature, acne) or asymptomatic hyperandrogenemia (non-classic CAH). Classic CAH is characterized by impaired cortisol and mineralocorticoid biosynthesis, which triggers adrenocorticotropic hormone (ACTH) hyper-secretion and accumulation of adrenal androgens. Glucocorticoid treatment of patients with classic CAH focuses on cortisol replacement and prevention of the ACTH-driven androgen excess. Current conventional glucocorticoid treatment regimens (short or long-acting agents dosed once, twice or thrice daily) have failed to simulate physiological cortisol secretion and suppress adrenal androgen overproduction, without supraphysiologic replacement. Short-term overtreatment with glucocorticoids can lead to iatrogenic Cushing syndrome and long-term use has been associated with the development of obesity, visceral adiposity, insulin resistance and osteoporosis. Isolated case reports have provided evidence that continuous subcutaneous hydrocortisone infusion (CSHI) can mimic physiologic cortisol release and lead to improved CAH control at doses similar to or lower than the traditional treatment. This pilot study aims to test the hypothesis that difficult-to-treat adult patients with classic CAH will have better adrenal androgen control and improved CAH and glucocorticoid-related comorbidities, when they receive near-physiologic cortisol replacement therapy via CSHI compared to conventional glucocorticoid treatment. In addition, this study will provide information on the safety and tolerability of CSHI, and will generate data that will be used in the design of future pediatric studies.

Connect with a study center

National Institutes of Health Clinical Center, 9000 Rockville Pike
Bethesda, Maryland 20892
United States
Site Not Available

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