Mode
Text Size
Log in / Sign up
Phase 4 N=20 Randomized Quadruple-blind Treatment

Effect of Exenatide in Obese Patients With Accelerated Gastric Emptying

Obesity

Enrolled (actual)
20
Serious AEs
0.0%
Results posted
Aug 2016
Primary outcome: Primary: Gastric Emptying Half-time (T 1/2) of Solids — 187; 86 minutes — p=<.001

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Exenatide (Drug); Placebo (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Mayo Clinic
Primary completion
Mar 2015

Outcome Measures

OutcomeResultp-value
PRIMARY
Gastric Emptying Half-time (T 1/2) of Solids
187; 86 <.001 sig
SECONDARY
Percentage of Gastric Contents Emptied at 1 Hour
12.4; 38.2 <.001 sig
SECONDARY
Change in Body Weight
-0.95; -0.55 0.23
SECONDARY
Satiation Expressed as Volume to Fullness
705; 675
SECONDARY
Maximum Tolerated Volume
1244; 1052
SECONDARY
Buffet Meal Intake (kcal)
977; 1110
SECONDARY
Aggregate Satiation Symptom Score
145; 172

Summary

The overall goal of this study was to determine the effect of exenatide on gastric emptying, satiety and satiation in obese participants. The hypothesis in this study was that exenatide retards gastric emptying in obese patients with baseline accelerated gastric emptying.

Eligibility Criteria

Inclusion Criteria

  • Obese subjects with BMI> 30 Kg/m^2: Otherwise healthy individuals who are not currently on treatment for cardiac, pulmonary, gastrointestinal, hepatic, renal, hematological, neurological, endocrine (other than hyperglycemia not requiring medical therapy) and unstable psychiatric disease.
  • Women of childbearing potential will have negative pregnancy test before initiation of medication.
  • Gastric emptying (GE): Accelerated GE T1/2 35 %

Exclusion Criteria

  • Type 1 or type 2 diabetes mellitus diagnosed according to American Diabetes Association criteria
  • Unstable heart disease as evidenced by ongoing angina
  • Congestive heart failure
  • Concomitant use of appetite suppressants (i.e., caffeine based or diethylpropion) or orlistat (Xenical®)
  • Uncontrolled hypertension (Blood pressure greater than 160/90 mmHg)
  • Use of anti-diabetic drugs including metformin,
  • History of nephrolithiasis,
  • Recurrent major depression, presence or history of suicidal behavior or ideation with intent to act, and current substantial depressive symptoms (Patient Health Questionnaire (PHQ-9) total score ≥10).
  • Gastroparesis
  • Inflammatory bowel disease or irritable bowel syndrome
  • Malignancy treated with chemotherapy within the past 3 years
  • History of pancreatitis
  • Renal insufficiency (eGFR less than 50 ml/min)
  • Concomitant use of monoamine oxidase inhibitors (i.e., phenelzine, selegiline), serotonergic agents, and other centrally acting appetite suppressants
  • Significant psychiatric dysfunction based upon screening with the Hospital Anxiety and Depression Scale (HADS) self-administered alcoholism screening test (SAAST, substance abuse) and the questionnaire on eating and weight patterns (binge eating disorders and bulimia). If such a dysfunction is identified by a HADS score ≥11 in any of the subscales or difficulties with substance or eating disorders, the participant will be excluded and given a referral letter to his/her primary care doctor for further appraisal and follow-up.
  • Intake of medication that could interfere with the interpretation of the study or cause drug interaction (i.e., ketoconazole, erythromycin). Specifically, birth control pill, estrogen replacement therapy, and thyroxine replacement are permissible.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02160990). 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.

Back to search