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Is Pentoxifylline Able to Improve Olfactory Sensitivity?

Agapurin Retard Used in Patients With Smell Disorder- A Post-marketing Observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00660868
Enrollment
7
Registered
2008-04-17
Start date
2009-11-30
Completion date
2016-01-31
Last updated
2016-02-05

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

Conditions

Olfaction Disorders

Keywords

smell, olfaction, olfactory sensitivity, smell loss, chemoreception

Brief summary

Signal processing in the olfactory neuron could be influenced by inhibition of enzymes like phosphodiesterase. Pentoxifylline is a unspecific phosphodiesterase inhibitor. The hypothesis is that pentoxifylline could lead to increased sensitivity to odors.

Detailed description

Olfactory signal processing is conducted by a G-protein linked increase of intracellular concentration of adenosine 3´,5´-cyclic monophosphate (cAMP). In the cilia of olfactory sensory neurons (OSN) cAMP is degraded by phosphodiesterase 1C2 (PDE1C2). Inhibition of PDE1C2 could result in an increased response of OSN to chemical stimuli. Aim of the present prospective post-marketing surveillance study was to investigate the impact of pentoxifylline, an unspecific phosphodieasterase inhibitor, on olfactory function.

Interventions

DRUGPentoxifylline retard 400mg

Agapurin retard 400mg 3/day per os for 3 weeks

Sponsors

Technische Universität Dresden
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* hyposmic or functionally anosmic patients TDI-score \<31 * age: 18-50 years * odor threshold: better than 1 * cause of smell loss: post traumatic, postinflammatory, idiopathic

Exclusion criteria

* normosmic patients, * patients with contraindications for application of pentoxifylline * patients that cannot give written agreement to the study * patients under 18 years and over 50 years of age

Design outcomes

Primary

MeasureTime frame
TDI-scoreat day 0 and follow up after 3 weeks

Secondary

MeasureTime frame
odor threshold odor discrimination odor identificationat day 0 and at follow up after 3 weeks

Countries

Germany

Outcome results

None listed

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