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Phase 2 N=8 Treatment

Comparison of Cortisol Pump With Standard Treatment for Congenital Adrenal Hyperplasia

Adrenal Insufficiency · Excess Androgen · Congenital Adrenal Hyperplasia (CAH)

Enrolled (actual)
8
Serious AEs
0.0%
Results posted
Nov 2017
Primary outcome: Primary: Number of Patients With 17-OHP Levels Equal or Below 1,200 ng/dL at 0700 — 0 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Hydrocortisone (Solucortef) (Drug); Insulin pump (Medtronic) (Device)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
National Institutes of Health Clinical Center (CC)
Primary completion
Dec 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Patients With 17-OHP Levels Equal or Below 1,200 ng/dL at 0700
PRIMARY
Number of Patients With 17-OH Progesterone Levels Equal or Below 1,200 ng/dL at 0700
3
SECONDARY
Participants Mean Level of 17-OHP at 0700
2150 0.021 sig
SECONDARY
Participants Mean Level of 17-OHP at 0700
2150 0.021 sig
SECONDARY
Participants Mean Level of 17-OHP Area Under the Curve (AUC) - 24 Hours
25.7 0.027 sig
SECONDARY
Participants Mean Level of 17-OHP Area Under the Curve (AUC) - 24 Hours
25.7 0.027 sig
SECONDARY
Participants Mean Level of 17-OHP Area Under the Curve (AUC) - Daytime (0700-1500)
6.8 0.008 sig
SECONDARY
Participants Mean Level of 17-OHP Area Under the Curve (AUC) - Daytime (0700-1500)
6.8 0.008 sig
SECONDARY
Participants Mean Level of 17-OHP Area Under the Curve (AUC) - Midday (1500 - 2300)
7.5 0.012 sig
SECONDARY
Participants Mean Level of 17-OHP Area Under the Curve (AUC) - Midday (1500 - 2300)
7.5 0.012 sig
SECONDARY
Participants Mean Level of 17-OHP Area Under the Curve (AUC) - Nighttime (2300 - 0700)
11.4 0.157
SECONDARY
Participants Mean Level of 17-OHP Area Under the Curve (AUC) - Nighttime (2300 - 0700)
11.4 0.157
SECONDARY
Participants Mean Level of Androstenedione at 0700
317 0.015 sig
SECONDARY
Participants Mean Level of Androstenedione at 0700
317 0.015 sig
SECONDARY
Participants Mean Level of Androstenedione Area Under the Curve (AUC) - 24 Hours
5.2 0.009 sig
SECONDARY
Participants Mean Level of Androstenedione Area Under the Curve (AUC) - 24 Hours
5.2 0.009 sig
SECONDARY
Participants Mean Level of Androstenedione Area Under the Curve (AUC) - Daytime (0700-1500)
1.8 0.008 sig
SECONDARY
Participants Mean Level of Androstenedione Area Under the Curve (AUC) - Daytime (0700-1500)
1.8 0.008 sig
SECONDARY
Participants Mean Level of Androstenedione Area Under the Curve (AUC) - Midday (1500 - 2300)
1.6 0.009 sig
SECONDARY
Participants Mean Level of Androstenedione Area Under the Curve (AUC) - Midday (1500 - 2300)
1.6 0.009 sig
SECONDARY
Participants Mean Level of Androstenedione Area Under the Curve (AUC) - Nighttime (2300 - 0700)
1.8 0.043 sig
SECONDARY
Participants Mean Level of Androstenedione Area Under the Curve (AUC) - Nighttime (2300 - 0700)
1.8 0.043 sig
SECONDARY
Participants Mean Level of ACTH at 0700
139 0.024 sig
SECONDARY
Participants Mean Level of ACTH at 0700
139 0.024 sig
SECONDARY
Participants Mean Level of ACTH Area Under the Curve (AUC) - 24 Hours
1087 0.031 sig
SECONDARY
Participants Mean Level of ACTH Area Under the Curve (AUC) - 24 Hours
1087 0.031 sig
SECONDARY
Participants Mean Level of ACTH Area Under the Curve (AUC) - Daytime (0700-1500)
340 0.005 sig
SECONDARY
Participants Mean Level of ACTH Area Under the Curve (AUC) - Daytime (0700-1500)
340 0.005 sig
SECONDARY
Participants Mean Level of ACTH Area Under the Curve (AUC) - Midday (1500 - 2300)
183 0.004 sig
SECONDARY
Participants Mean Level of ACTH Area Under the Curve (AUC) - Midday (1500 - 2300)
183 0.004 sig
SECONDARY
Participants Mean Level of ACTH Area Under the Curve (AUC) - Nighttime (2300 - 0700)
564 0.524
SECONDARY
Participants Mean Level of ACTH Area Under the Curve (AUC) - Nighttime (2300 - 0700)
564 0.524
SECONDARY
Participants Mean Progesterone Levels at 0700
9.5
SECONDARY
Participants Mean Progesterone Level at 0700
0.8 0.007 sig
SECONDARY
Participants Mean Level of Progesterone Area Under the Curve (AUC) - 24 Hours
13.7 0.084
SECONDARY
Participants Mean Level of Progesterone Area Under the Curve (AUC) - 24 Hours
13.7 0.084
SECONDARY
Participants Mean Level of Progesterone Area Under the Curve (AUC) - Daytime (0700-1500)
4.2 0.057
SECONDARY
Participants Mean Level of Progesterone Area Under the Curve (AUC) - Daytime (0700-1500)
4.2 0.057
SECONDARY
Participants Mean Level of Progesterone Area Under the Curve (AUC) - Midday (1500 - 2300)
5.5 0.103
SECONDARY
Participants Mean Level of Progesterone Area Under the Curve (AUC) - Midday (1500 - 2300)
5.5 0.103
SECONDARY
Participants Mean Level of Progesterone Area Under the Curve (AUC) - Nighttime (2300 - 0700)
4.0 0.070
SECONDARY
Participants Mean Level of Progesterone Area Under the Curve (AUC) - Nighttime (2300 - 0700)
4.0 0.070
SECONDARY
Participant Lean Body Mass
64.3
SECONDARY
Participant Lean Body Mass
64.3

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 ELIGIBILITY Inclusion criteria 1. Men and women 18 years of age or older with classic congenital adrenal hyperplasia (21-Hydroxylase deficiency) 2. High adrenal androgens in the blood, and 3. One or more of the following conditions: obesity, fatty liver, risk for diabetes, low bone mass, inability to tolerate cortisol pills Exclusion criteria 1. Pregnancy 2. Breast feeding 3. Use of inhaled or oral steroids for diseases other than CAH 4. Use of estrogen-containing birth control pills 5. Use of medicines that cross-react with hydrocortisone 6. Use of stress dose steroids for illness during the last 30 days prior to joining the study

Eligibility Criteria

  • INCLUSION CRITERIA:
  • Patients with known classic CAH due to 21-hydroxylase deficiency as evidenced by hormonal and genetic testing
  • Male or female patients 18 years or older
  • Females must have a negative pregnancy test initially and at all visits. Sexually active females must be using a medically acceptable method of contraception.
  • Patients with elevated adrenal androgens (defined as 17-OHP >1200 ng/dL and androstenedione >210 ng/dL)
  • One or more co-morbidities:
  • 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 2.6 in adults17.
  • Osteopenia [bone mineral density by DEXA (at the spine, hip, or forearm) with T-score of -1 to -2.5) or osteoporosis (bone mineral density by DEXA (at the spine, hip, or forearm) 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 CRITERIA

  • Co-morbid conditions requiring daily administration of medications that induce hepatic enzymes 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 of recruitment
  • Patients who required stress dose glucocorticoids for an illness within 4 weeks of recruitment
  • 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
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01859312). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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