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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04923425
Other study ID # 18936 CairoU
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 22, 2020
Est. completion date October 7, 2020

Study information

Verified date June 2021
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Identify possible modulators for developing gustatory dysfunction among a sample of depressed Egyptian adults (age from 20 to 50 years old) under anti-depressants therapy ( for at least 3 months) using a questionnaire ( appendix) with a binary measuring unit (yes/no).


Description:

PECO - P Population: depressed Egyptian adults under anti-depressants therapy - E1 Exposure 1: commonly prescribed tricyclic antidepressants (Imipramine, Amitriptyline, Clomipramine HCL) - E2 Exposure 2: commonly prescribed Selective Serotonin Re-uptake inhibitors antidepressants ( Fluoxetine, Fluvoxamine, Sertraline, Citalopram, Paroxetine) - C control (non exposure) : non-pharmacological treatment ( psychotherapy) - O Outcome: Identify possible gustatory dysfunction modulators among these patients using a questionnaire ( appendix) with a binary measuring unit (yes/no).


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date October 7, 2020
Est. primary completion date August 8, 2020
Accepts healthy volunteers No
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria: - • Depressed Egyptian adults under antidepressants therapy for at least 3 months/non-pharmacological treatment( psychotherapy) - Age from 20 to 50 years old Exclusion Criteria: - Antipsychotics - Hypnotics - Anticonvulsants - Ages other than the mentioned • Olfactory dysfunction - Chemosensory dysfunction

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Egypt Faculty of Dentistry, Cairo University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Gustatory dysfunction modulators -C.M will use an assessment questionnaire (appendix) to assess possible modulators for developing gustatory dysfunction including a number of short-term and long-term factors such as body mass, gender, age, local and systemic diseases, excessive alcohol drinking, drug dependence, smoking, state of oral hygiene, consumption of some foods or drugs during a period of 7months from February 2020 till August 2020
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