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Research Study for Children With Salt Wasting Congenital Adrenal Hyperplasia

Primary Purpose

Adrenal Hyperplasia, Congenital

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Hydrocortisone sodium acetate
Sponsored by
Baylor College of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Adrenal Hyperplasia, Congenital focused on measuring Salt Wasting Congenital Adrenal Hyperplasia, Subcutaneous Hydrocortisone

Eligibility Criteria

3 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children with salt wasting CAH otherwise healthy without other chronic disease
  • Age: between 3 and 18 years of age
  • Body weight 23 kg (50 lbs) or above
  • Hemoglobin equal to or higher than 12 g/dl before the study
  • Supportive family environment

Exclusion Criteria:

  • Age less than 3 or older than 18 years at the time of study
  • Other chronic disease
  • Hemoglobin less than 12 g/dl
  • Non-supportive family
  • Allergy to local anesthetics

Criteria for study termination: If the subject's parents are unable to manage/operate the pump, the subject will be withdrawn from the study.

Sites / Locations

  • BCM, Texas Children's Hospital Clinic and General Clinical Research Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

1 (Hydrocortisone sodium acetate)

Arm Description

Subcutaneous administration of Hydrocortisone sodium acetate via insulin pump

Outcomes

Primary Outcome Measures

Serum 17-OHP concentration in the morning

Secondary Outcome Measures

serum steroid hormone profiles
serum blood glucose
serum sodium

Full Information

First Posted
September 12, 2007
Last Updated
September 10, 2015
Sponsor
Baylor College of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT00529841
Brief Title
Research Study for Children With Salt Wasting Congenital Adrenal Hyperplasia
Official Title
A Novel Therapeutic Modality for Congenital Adrenal Hyperplasia
Study Type
Interventional

2. Study Status

Record Verification Date
September 2015
Overall Recruitment Status
Completed
Study Start Date
January 2007 (undefined)
Primary Completion Date
September 2008 (Actual)
Study Completion Date
September 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Baylor College of Medicine

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to develop a more physiological approach to the management of children and adolescents with salt wasting Congenital Adrenal Hyperplasia. We will administer the glucocorticosteroid via insulin infusion pump to see whether this treatment will improve the serum hormone concentrations.
Detailed Description
The adrenal gland is a small organ of the body. It produces very important chemicals called hormones. One of these hormones, cortisol (the stress hormone) helps the body fight diseases. The other hormone is the aldosterone helps to maintain the normal amount of salt and water in the body. The third type of hormones are the androgens or male hormones, which cause some of the changes during puberty, like the growth of body hair and pimples. The salt wasting Congenital Adrenal Hyperplasia or CAH disease is a disease of the adrenal gland. Patients with this disease cannot make cortisol or the aldosterone. As a result, their body cannot fight diseases and cannot keep normal amounts of salt and water in the body. At the same time, the gland makes too much of the male hormones, which is bad for the body because too much male hormone slows down growth, increases the growth of body hair, and causes pimples and abnormal period in girls. Patients with this disease have to take medications every day. However, the treatment does not work very well, because usually the patients do not have the right amount of hormone in their body. Usually the body gets too much hormone right after taking the pills. A couple of hours later the body has too little of the hormones, because in the meantime the body gets rid of the medication.The healthy adrenal gland makes the hormones throughout the day in different amounts. The patients with this disease take the medication only a couple of times a day. They take the Florinef tablet once a day and the Cortisol tablet two or three times a day. The treatment that we use today by mouth cannot copy the natural hormone productions of the adrenal gland. Because of this it does not make much of a difference in the patient's life. We would like to improve the treatment and find out the effect of a new treatment. In this study we will try to imitate the body's normal hormone production and will give the medication via an insulin pump to see if this treatment method will decrease the male hormones in the blood. This study will help us to develop a new and better treatment for children and adolescents.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adrenal Hyperplasia, Congenital
Keywords
Salt Wasting Congenital Adrenal Hyperplasia, Subcutaneous Hydrocortisone

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
7 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1 (Hydrocortisone sodium acetate)
Arm Type
Experimental
Arm Description
Subcutaneous administration of Hydrocortisone sodium acetate via insulin pump
Intervention Type
Drug
Intervention Name(s)
Hydrocortisone sodium acetate
Other Intervention Name(s)
Solu-Cortef injection
Intervention Description
Subcutaneous administration of medication via insulin pump
Primary Outcome Measure Information:
Title
Serum 17-OHP concentration in the morning
Time Frame
11 days
Secondary Outcome Measure Information:
Title
serum steroid hormone profiles
Time Frame
11 days
Title
serum blood glucose
Time Frame
study days 2,3 and 11
Title
serum sodium
Time Frame
study days 2,3 and 11

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children with salt wasting CAH otherwise healthy without other chronic disease Age: between 3 and 18 years of age Body weight 23 kg (50 lbs) or above Hemoglobin equal to or higher than 12 g/dl before the study Supportive family environment Exclusion Criteria: Age less than 3 or older than 18 years at the time of study Other chronic disease Hemoglobin less than 12 g/dl Non-supportive family Allergy to local anesthetics Criteria for study termination: If the subject's parents are unable to manage/operate the pump, the subject will be withdrawn from the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Morey W Haymond, MD
Organizational Affiliation
Baylor College of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
BCM, Texas Children's Hospital Clinic and General Clinical Research Center
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
1986026
Citation
Esteban NV, Loughlin T, Yergey AL, Zawadzki JK, Booth JD, Winterer JC, Loriaux DL. Daily cortisol production rate in man determined by stable isotope dilution/mass spectrometry. J Clin Endocrinol Metab. 1991 Jan;72(1):39-45. doi: 10.1210/jcem-72-1-39.
Results Reference
background
PubMed Identifier
8501158
Citation
Kerrigan JR, Veldhuis JD, Leyo SA, Iranmanesh A, Rogol AD. Estimation of daily cortisol production and clearance rates in normal pubertal males by deconvolution analysis. J Clin Endocrinol Metab. 1993 Jun;76(6):1505-10. doi: 10.1210/jcem.76.6.8501158.
Results Reference
background
PubMed Identifier
10469004
Citation
Speiser PW. Toward better treatment of congenital adrenal hyperplasia. Clin Endocrinol (Oxf). 1999 Sep;51(3):273-4. doi: 10.1046/j.1365-2265.1999.00780.x. No abstract available.
Results Reference
background
PubMed Identifier
2247119
Citation
Cutler GB Jr, Laue L. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. N Engl J Med. 1990 Dec 27;323(26):1806-13. doi: 10.1056/NEJM199012273232605. No abstract available.
Results Reference
background
PubMed Identifier
3871229
Citation
Winterer J, Chrousos GP, Loriaux DL, Cutler GB Jr. Effect of hydrocortisone dose schedule on adrenal steroid secretion in congenital adrenal hyperplasia. J Pediatr. 1985 Jan;106(1):137-42. doi: 10.1016/s0022-3476(85)80486-8.
Results Reference
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PubMed Identifier
1645237
Citation
Wallace WH, Crowne EC, Shalet SM, Moore C, Gibson S, Littley MD, White A. Episodic ACTH and cortisol secretion in normal children. Clin Endocrinol (Oxf). 1991 Mar;34(3):215-21. doi: 10.1111/j.1365-2265.1991.tb00297.x.
Results Reference
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PubMed Identifier
16817818
Citation
Merza Z, Rostami-Hodjegan A, Memmott A, Doane A, Ibbotson V, Newell-Price J, Tucker GT, Ross RJ. Circadian hydrocortisone infusions in patients with adrenal insufficiency and congenital adrenal hyperplasia. Clin Endocrinol (Oxf). 2006 Jul;65(1):45-50. doi: 10.1111/j.1365-2265.2006.02544.x.
Results Reference
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PubMed Identifier
16522704
Citation
Lukert BP. Editorial: glucocorticoid replacement--how much is enough? J Clin Endocrinol Metab. 2006 Mar;91(3):793-4. doi: 10.1210/jc.2005-2737. No abstract available. Erratum In: J Clin Endocrinol Metab. 2006 Jun;91(6):2073.
Results Reference
background
Citation
Claude J.Migeon. Can the Long Range Results of the Treatment of Congenital Adrenal Hyperplasia be improved? JCEM 1996 Vol 81, No 9 3187-3189
Results Reference
background
PubMed Identifier
8855797
Citation
Laue L, Merke DP, Jones JV, Barnes KM, Hill S, Cutler GB Jr. A preliminary study of flutamide, testolactone, and reduced hydrocortisone dose in the treatment of congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1996 Oct;81(10):3535-9. doi: 10.1210/jcem.81.10.8855797.
Results Reference
background
PubMed Identifier
15355454
Citation
Mah PM, Jenkins RC, Rostami-Hodjegan A, Newell-Price J, Doane A, Ibbotson V, Tucker GT, Ross RJ. Weight-related dosing, timing and monitoring hydrocortisone replacement therapy in patients with adrenal insufficiency. Clin Endocrinol (Oxf). 2004 Sep;61(3):367-75. doi: 10.1111/j.1365-2265.2004.02106.x.
Results Reference
background
Citation
Sheila K.Gunn et al Subcutaneous Hydrocortisone Delivery mimics Physiologic Cortisol Concentrations, Poster, Endocrine Society Meeting 2000
Results Reference
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Research Study for Children With Salt Wasting Congenital Adrenal Hyperplasia

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