Skip to content

Use of a Phosphodiesterase Type 5 Inhibitor to Improve Anabolic Resistance in Older Adults

Use of a Phosphodiesterase Type 5 Inhibitor to Improve Anabolic Resistance in Older Adults

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05458232
Enrollment
0
Registered
2022-07-14
Start date
2023-01-20
Completion date
2023-01-20
Last updated
2024-11-04

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

Conditions

Sarcopenia

Brief summary

This study will be the first demonstration of the utility and feasibility of Phosphodiesterase Type 5 inhibitor as an effective pharmacological therapy for improving anabolic resistant states.

Interventions

Subjects will ingest one 5mg tablet of tadalafil each evening for 14 days.

Sponsors

University of Arkansas
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
60 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Ages 60-75 yrs * Recently prescribed 5mg of tadalafil daily for clinical purposes

Exclusion criteria

* History of diabetes * history of hypotension including orthostatic hypotension * History of malignancy or chemo/radiation therapy in the 6 months prior to enrollment * History of short gut syndrome, gastrointestinal bypass/reduction surgery (Lap band, gastric sleeve, etc.) * Subjects who cannot refrain from using protein or amino acid supplements for 7 days prior to Visit 2 and 3. * Alcohol consumption of ≥ 5 units/servings per day * Concomitant use of * oral or injectable corticosteroids * testosterone, insulin like growth factor-1, or similar anabolic agent * riociguat (Adempas) * nitroglycerin * isosorbide dinitrate (Isordil) * isosorbide mononitrate (Imdur, Monoket) * doxazosin (Cardura) * prazosin (Minipress) * terazosin (Hytrin) * Any other disease or condition that would place the subject at increased risk of harm if they were to participate, at the discretion of the study physician

Design outcomes

Primary

MeasureTime frameDescription
Change in maximal voluntary contraction of lower leg.14 daysLower leg strength using a dynamometer; performed both before and after 14 days of tadalafil

Secondary

MeasureTime frameDescription
Change in muscle Fatigue14 daysA test of lower leg muscular endurance using a dynamometer; performed both before and after 14 consecutive days of tadalafil.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026