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Recruiting

NCT Number: NCT06571500

Growth Hormone Resistance of Beta-cells in People With a Family History of Type 2 Diabetes

The purpose of the research study is to better understand how beta-cells (cells in the pancreas that make insulin and help regulate blood sugar) respond to growth hormone in people with a family history of type 2 diabetes at the University of Missouri. Our aim is to advance understanding of how growth hormone affects beta-cells and risk factors for developing type 2 diabetes.

Recruiting

Interested in participating?

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Key information

Age range

18 year–59 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Missouri School of Medicine

Columbia, Missouri, 65212, United States

Location status: Recruiting

Location contact

Bettina Mittendorfer

CONTACT

[email protected]

573-882-9377

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • 18 to 59 years old
  • body mass index ≥30.0 kg/m2 and <45.0 kg/m2

Additional, group-specific inclusion criteria:

  • Family history of type 2 diabetes: first degree relative with type 2 diabetes
  • Control group: no family history of type 2 diabetes

Exclusion criteria

  • Pregnant, planning to become pregnant during the study, or breastfeeding
  • Current diagnosis or history of type 1 or type 2 diabetes
  • Use of medications that can impact the study outcomes (e.g., GLP-1 receptor agonists)
  • History of bariatric surgery
  • Known, uncontrolled hypothyroidism
  • History of intracranial hypertension, including papilledema, or a condition that increases the risk of developing intracranial hypertension, such as Turner Syndrome, Prader-Willi Syndrome, or renal impairment
  • Current cancer or cancer that has been in remission less than 5 years
  • First degree relative with type 1 diabetes diagnosis
  • Evidence of significant anemia or significant end organ dysfunction (e.g., liver, kidney, heart disease)
  • Alcohol use disorder, use of controlled substances, or smoking >2 cigarettes per day
  • Greater than 3% weight loss within three months of screening or engaged in regular (≥3 days per week), continuous moderate- or high-intensity exercise of ≥30 min duration
  • Mentally disabled persons, prisoners, and persons with inability to grant voluntary informed consent

Treatment and study plan

Primary outcomes

  1. Beta-cell function

    Time frame: before and 7 days after rhGH administration

    Insulin secretion rate in relationship to plasma glucose

Study contacts

Contact information is provided by the study sponsor or research team.

Amanda Heider

CONTACT

[email protected]

573-884-6852

Vasavi Shabrish, PhD

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

University of Missouri-Columbia

Other

Registry information

Acronym: GHRB-B

Important dates

Study start
2025
Primary completion
2028
Study completion
2030
First posted
Aug 26, 2024
Registry last updated
May 11, 2026

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.

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