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The effect of training on the improvement of olfactory disorder and sexual satisfaction in patients with anosmia/hyposmia

The effect of olfactory training on the improvement of olfactory disorder and its relation with sexual satisfaction in patients with post traumatic anosmia/hyposmia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017102034225N1
Enrollment
120
Registered
2017-10-20
Start date
2017-07-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Post traumatic Anosmia/Hyposmia. Sequelae of injuries, of poisoning and of other consequences of external causes

Interventions

Intervention 1: The training group will take olfactory training through 12 weeks according to the Henning we have four groups are classified:. 1, Phenyl ethyl alcohol 2, Eucalyptol 3, Citronellal 4,
Treatment - Other
The training group will take olfactory training through 12 weeks according to the Henning we have four groups are classified:. 1, Phenyl ethyl alcohol 2, Eucalyptol 3, Citronellal 4, Eugenol we

Sponsors

Research Center of the ear, throat, nose and head and neck of Iran
Lead Sponsor

Eligibility

Sex/Gender
All
Age
23 Years to 43 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: married; having sex with a spouse and age between the ages of 23 to 43; having post traumatic anosmia/hyposmia. Exclusion criteria: congenital anomalies(Kalman Syndrome); single; having neurological diseases such as Parkinson's and Alzheimer's; Diabetes; smoking; sinonasal disease; acute nasal disease such as infection; pregnancy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Olfaction. Timepoint: at the start of study, one day after complete the intervention. Method of measurement: Sniffin sticks tests.

Secondary

MeasureTime frame
Sexual satisfaction. Timepoint: At the start of study, one day after complete the intervention. Method of measurement: Larson sexual satisfaction questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Rafie Alizadeh Miran

Research Center of the ear, throat, nose and head and neck of Iran University of Medical Sciences

nafiseh.alizadeh@gmail.com+98 21 64351

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026