Skip to main content
OpenTrials
Completed

NCT Number: NCT03842501

Effects of the GOLO Weight Management Program With and Without Release Supplement on Weight and Metabolic Parameters in Subjects With Obesity

This randomized, double-blind placebo-controlled study was intended to measure the effects of the GWMP with Release supplement versus GWMP with placebo supplement in a representative group of obese subjects with or without diabetes at one outpatient medical practice.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Buynak Clinical Research

Valparaiso, Indiana, 46385, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years and ≤ 80 years
  • Body mass index (BMI) ≥ 30 and ≤ 60 kg/m2
  • Have the ability to engage in at least 15 minutes of moderate physical activity such as brisk walking
  • Willing to comply with study procedures described herein

Exclusion criteria

  • Current diagnosis of type 1 diabetes
  • Subjects with a history of hypoglycemia
  • A history of an eating disorder as defined by the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5)
  • Known allergy to any of the components in the Release supplement
  • A history of prior surgery for weight loss
  • Currently taking injectable medications to control diabetes, including insulin and GLP-1 agonists
  • Currently pregnant or breastfeeding or have had a baby within the last six weeks
  • Planning to become pregnant in the next three months. Women of child bearing potential must be willing and able to use adequate and reliable contraception throughout the study (e.g. abstinence or barrier with additional spermicidal foam or jelly, or the use of intrauterine device or hormonal contraception).
  • Uncontrolled hypertension at screening defined as Systolic blood pressure greater than 180 mmHG or Diastolic blood pressure greater than 110 mmHG
  • Current clinical diagnosis or signs and symptoms of unstable (in the opinion of the principle investigator) heart, kidney or liver disease, cancer, or chronic neurological disease.
  • Current participation in any other weight loss or weight management program
  • Currently taking weight loss medications, or medications or supplements known to be associated with significant weight loss or weight gain
  • Has any condition that, in the opinion of the investigator, would make participation in this study not in the best interest of the subject or that could prevent, limit or confound the protocol-specified assessments. Examples include: history of diabetic ketoacidosis; active chronic liver disease or cirrhosis; chronic autoimmune disease; inflammatory bowel disease, colonic ulceration, partial intestinal obstruction, subjects predisposed to intestinal obstruction; chronic intestinal diseases associated with marked disorders of digestion or absorption

-

Treatment and study plan

Release Supplement

Dietary Supplement

Calorie reduced diet plus Release supplement

Placebo

Dietary Supplement

Calorie reduced diet plus Placebo

Primary outcomes

  1. Change in weight from baseline

    Time frame: 13 weeks

Secondary outcomes

  1. Change in waist circumference from baseline

    Time frame: 13 weeks

  2. Change in fasting glucose from baseline

    Time frame: 13 weeks

  3. Change in Hemoglobin A1C from baseline

    Time frame: 13 weeks

Sponsors and collaborators

Lead sponsor

Golo

Industry

Registry information

Official study title

A Randomized, Double-blind, Placebo-controlled Study Evaluating the Effects of the GOLO Weight Management Program With and Without Release Supplement on Weight and Metabolic Parameters in Subjects With Obesity

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Feb 15, 2019
Registry last updated
Feb 15, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.