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Effects of Exenatide on Obesity and/or Diabetes Mellitus Due to Hypothalamic Damage

Effects of Exenatide on Obesity and/or Diabetes Mellitus Due to Hypothalamic Damage

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01783717
Enrollment
10
Registered
2013-02-05
Start date
2012-12-31
Completion date
2015-07-31
Last updated
2013-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus, Hypothalamic Obesity

Brief summary

The purpose of this study is to examine the effect of exenatide on body weight and glycemic control in subjects with obesity and/or diabetes mellitus due to hypothalamic damage.

Detailed description

Patients with hypothalamus lesion caused by tumors in the hypothalamic region, such as craniopharyngioma and germ cell tumors, and inflammatory diseases are susceptible to develop severe obesity and diabetes mellitus. The occurrence of hypothalamic obesity in patients after surgery with or without radiotherapy for craniopharyngioma can be as high as 42-66%, and the incidence of type 2 diabetes mellitus of them is twice as much as healthy controls. Treatment of obesity and diabetes mellitus in this population is crucial for increasing morbidity and mortality. However, diet and exercise intervention has been proven useless in previous studies. Safe and effective medicine remains to be developed. Exenatide, a GLP-1 receptor agonist, which play an antihyperglycemic role through a variety of mechanisms, such as enhancing glucose-dependent insulin secretion, increasing beta cell mass and decreasing glucagon secretion, possesses a potent ability to induce satiety, slow gastric emptying and reduce food intake, resulting in weight loss both in diabetics and patients with simple obesity. Previous animal study has already shown GLP-1 agonist exendin-4 leads to reduction of weight and caloric intake in a rat model of hypothalamic obesity. Therefore, the investigators hypothesize exenatide treatment might lead to weight loss in hypothalamic obese patients and improve their glycemic control.

Interventions

DRUGExenatide

5mcg twice a day for 4 weeks increased to 10 mcg twice a day for 8 weeks

Sponsors

Huashan Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

1. Be between 18 and 55 years old; 2. Greater than 6 months post-treatment (including surgery, radiotherapy or chemotherapy) of craniopharyngioma or other diseases in the hypothalamic region; 3. BMI≧28kg/m2 and/or diabetes mellitus; 4. Greater than 3 months after adequate replacement therapy for hypothalamic-pituitary-adrenal (HPA) axis and hypothalamic-pituitary-thyroid (HPT) axis; 5. Sign informed consent document.

Exclusion criteria

1. Less than 6 months post surgery or radiotherapy or chemotherapy for craniopharyngioma or other diseases in the hypothalamic region; 2. Inadequate replacement for the HPA axis and HPT axis or undertaking adjustments of the kind or dose of the substitutive medicine; 3. Use of weight loss drugs or initiation of a weight loss program within past 3 months; 4. Use of GLP-1 agonists or analogues or dipeptidyl peptidase IV (DPP-IV) inhibitors within past 3 months; 5. History of bariatric surgery; 6. Diagnosed with simple obesity or diabetes mellitus prior to the hypothalamic disorders, and those diagnosed with type 1 diabetes mellitus; 7. With end-stage-renal diseases or history of kidney transplant or complicated with acute/chronic kidney failure (GFR≦30ml/min); 8. History of inflammatory bowel diseases or gastroparesis or other gastric mortility problems; 9. History of pancreatitis or chronic cholecystitis; 10. History of allergic reaction to exenatide or other medication components; 11. Undertaking warfarin; 12. Pregnant or lactating women; 13. Are participating in, or have participated in other drug clinical trials within past 3 months.

Design outcomes

Primary

MeasureTime frame
Change in body weight frome baseline to end of the study.3 months
BMIbaseline and 3 months
HbA1cbaseline and 3 months
Blood glucose level.3 months.
Beta cell function.baseline and 3 months
Insulin sensitivity.baseline and 3 months

Secondary

MeasureTime frame
Waistlinebaseline and 3 months
waistline/hipline ratiobaseline and 3 months
Ratio of body fatbaseline and 3 months
The amount of daily energy intakebaseline and 3 months
Resting energy expenditure (kcals per day)baseline and 3 months
Grade of metabolic equivalents (MET) scalesbaseline and 3 months
Hipline.baseline and 3 months

Countries

China

Contacts

Primary ContactZhang z yun
86-21-52888286

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026