search
Back to results

Effect of Growth Hormone in Metabolic Syndrome

Primary Purpose

Metabolic Syndrome

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Growth hormone
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metabolic Syndrome focused on measuring Metabolic syndrome

Eligibility Criteria

35 Years - 50 Years (Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria: Age 35 to 50 Chinese men Metabolic syndrome as defined according to 1998 World Health Organisation with modification using Asian definition for obesity (body mass index 25kg/m2, waist circumference 80cm in women and 90 cm in men) Low IGF-1 level or IGF-1 level in low normal range (<200 ug/L) Exclusion Criteria: Any malignancy within the past 5 years A diagnosis of acromegaly Uncontrolled hypertension (systolic blood pressure >180mmHg or diastolic blood pressure>105mmHg) A history of carpel tunnel syndrome Poor glycemic control (HbA1c>8%) Diabetic microangiopathy Previous cardiovascular event Anaemia as defined as haemoglobin <11g/dL Active thyroid diseases Any medical illness that will render the subject vulnerable to fluid retention state, e.g. renal impairment, heart failure or as judged by the investigators as ineligible to participate the study.

Sites / Locations

  • Prince of Wales Hospital, The Chinese University of Hong Kong

Outcomes

Primary Outcome Measures

Change in percentage of body fat from baseline.

Secondary Outcome Measures

Examine the percentage change from baseline in insulin sensitivity, various indices of metabolic syndrome of growth hormone treatment will be compared to placebo arm.

Full Information

First Posted
March 27, 2006
Last Updated
April 3, 2006
Sponsor
Chinese University of Hong Kong
search

1. Study Identification

Unique Protocol Identification Number
NCT00307411
Brief Title
Effect of Growth Hormone in Metabolic Syndrome
Official Title
Effects of Growth Hormone on Body Fat Distribution, Insulin Action and Cardiovascular Risk Factors in Middle-Aged Men With Metabolic Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
March 2006
Overall Recruitment Status
Unknown status
Study Start Date
August 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
July 2007 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Chinese University of Hong Kong

4. Oversight

5. Study Description

Brief Summary
Investigating the effect of low dose growth hormone therapy on body fat composition, insulin sensitivity and metabolic profiles in middle-aged men with metabolic syndrome and low insulin-like growth factor (IGF-1) level.
Detailed Description
Metabolic syndrome, a constellation of glucose intolerance, hypertension, dyslipidemia, obesity, pro-inflammatory and prothrombotic state culminating to development of premature cardiovascular diseases is a serious public health problem with significant impact on life expectancy, societal productivity and quality of life of those afflicted with it. Insulin resistance has been proposed as the key linking factor for the metabolic syndrome. Although the underlying mechanism for the development of insulin resistance, diabetes and metabolic syndrome is not fully understood, increasing evidence suggests that neurohormonal dysregulation plays a pivotal role in causing this growing health hazard. In our previous study of 307 middle-aged men, low insulin-like growth factor (IGF)-1 level was independently associated with insulin resistance and metabolic syndrome, especially amongst those with positive family history of diabetes. Replacement with growth hormone has been shown by other researchers to reduce body fat and improve metabolic profiles in patients with adult growth hormone deficiency and type 2 diabetes. We hypothesize that treatment with growth hormone can lead to reduction of body fat, insulin resistance and cardiovascular risk factors in men with metabolic syndrome. This will be a 12-month prospective, randomized, double-blind, placebo-controlled study using growth hormone treatment in middle-aged men with metabolic syndrome. The primary outcome measure will be body fat distribution, including changes in visceral and mesenteric fat, whereas secondary outcome measure will be insulin sensitivity, and tertiary outcome will be variable parameters of metabolic syndrome. The results of this study will have important impact on the treatment of patients with metabolic syndrome, and our understanding of the role of growth hormone in the pathogenesis of insulin resistance, diabetes and metabolic syndrome.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metabolic Syndrome
Keywords
Metabolic syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
32 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Growth hormone
Primary Outcome Measure Information:
Title
Change in percentage of body fat from baseline.
Secondary Outcome Measure Information:
Title
Examine the percentage change from baseline in insulin sensitivity, various indices of metabolic syndrome of growth hormone treatment will be compared to placebo arm.

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 35 to 50 Chinese men Metabolic syndrome as defined according to 1998 World Health Organisation with modification using Asian definition for obesity (body mass index 25kg/m2, waist circumference 80cm in women and 90 cm in men) Low IGF-1 level or IGF-1 level in low normal range (<200 ug/L) Exclusion Criteria: Any malignancy within the past 5 years A diagnosis of acromegaly Uncontrolled hypertension (systolic blood pressure >180mmHg or diastolic blood pressure>105mmHg) A history of carpel tunnel syndrome Poor glycemic control (HbA1c>8%) Diabetic microangiopathy Previous cardiovascular event Anaemia as defined as haemoglobin <11g/dL Active thyroid diseases Any medical illness that will render the subject vulnerable to fluid retention state, e.g. renal impairment, heart failure or as judged by the investigators as ineligible to participate the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Alice PS Kong, M.B.,Ch.B.
Phone
852-2632 3123
Email
kongps@yahoo.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alice PS Kong, M.B.,Ch.B.
Organizational Affiliation
Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Prince of Wales Hospital, The Chinese University of Hong Kong
City
Hong Kong SAR
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alice PS Kong, M.B.,Ch.B.
Phone
852-2632 3123
Email
kongps@yahoo.com
First Name & Middle Initial & Last Name & Degree
Alice PS Kong, M.B.,Ch.B.

12. IPD Sharing Statement

Learn more about this trial

Effect of Growth Hormone in Metabolic Syndrome

We'll reach out to this number within 24 hrs