Comparison of muscle strength, cognitive ability, and sleep quality before and after switching to the somapacitan once-weekly preparation and with the continuous daily administration of the somatropin preparation for patients with adult growth hormone deficiency during daily administration of the somatropin preparation (single-facility, observational study)
Not Applicable
Recruiting
- Conditions
- Adult Growth Hormone deficiency
- Registration Number
- JPRN-UMIN000046952
- Lead Sponsor
- Kobe University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
1. Patients with severe renal dysfunction (eGFR less than 30 mL / min / 1.73 m2) 2. Pregnant and lactating patients
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method