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Study on the effects of GLP1 on hepatic lipid content in AGHD complicated with obesity

A single-center prospective observational study on the effects of GLP-1 analogs on hepatic fat content in adult growth hormone deficiency complicated with obesity

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1031240227
Enrollment
20
Registered
2024-07-23
Start date
2024-07-23
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Adult growth hormone deficiency Adult growth hormone deficiency

Interventions

none
None

Sponsors

Kubo Haremaru
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1, Severe Adult growth hormone deficiency 2, Patients scheduled for Wegovy administration with an indication for its use, 3, BMI of 27 kg/m2 or higher with at least two obesity-related health disorders, or a BMI of 35 kg/m2 or higher 4, Receiving nutritional counseling for more than 6 months 5, Undergoing growth hormone replacement therapy

Exclusion criteria

Exclusion criteria: 1, Patients with severe trauma or undergoing surgery 2, Excessive alcohol consumers (estimated ethanol intake more than 30 g/day for men, and more than 20 g/day for women) 3, Patients with other liver diseases that cannot be ruled out, including viral hepatitis, autoimmune hepatitis, and drug-induced hepatitis 4, Patients with severe liver disfunction or liver cirrhosis classified as Child-Pugh B or C 5, Patients infected with the hepatitis virus 6, Patients with obvious malignant tumors 7, Pregnant women or women who might be pregnant 8, Patients using implanted medical devices (such as pacemakers) 9, Individuals under 20 years old or over 80 years old 10, Patients with intellectual disabilities or language problems that prevent them from fully understanding the study 11, Patients who are judged to be unable to carry out this study by the principal investigator or research assistant.

Design outcomes

Primary

MeasureTime frame
The change in hepatic fat content (MRI-PDFF) from the beginning to the end of the study

Secondary

MeasureTime frame
1, The changes in parameters related to body composition from the beginning to the end of the study. 2, The changes in parameters related to each blood test item from the beginning to the end of the study. 3, The correlation between the change in MRI-PDFF and each parameter.

Contacts

Public ContactHaremaru Kubo

Kitasato University Hospital

kubo.haremaru@kitasato-u.ac.jp+81-42-778-8111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026