- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05343234
Drug Name Identification an Ignored Patient's Problem That Needs a Solution
Each of the recruited patient was given 3 different placebo drugs with 3 different mad up names to be taken for one month with different regiments.
The drug name resembled a real drug but with enough difference to prevent the patient from trying to buy it as a safety precaution. The name was printed on the box in English and Arabic letters. The coloured shape was printed to 2x2 cm dimension.
After one month the participants were intervened by a doctor blinded to the study. The doctor asked about the drug history of the patient. If the participant could remember the drug name and its correct regiment the doctor documented that. if the patent failed to remember the correct name and its regiment then the doctor asked the patient to try and remember anything about the drug.
Then the patient would be asked about the symbol on the drug and was it helpful for him in any way.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
A scoring system was used to evaluate pateints memory of the drugs used 0- 3 0 is the minimal score and will be given if no recall of any drug name and 3 is the maximum score and will be given if the patient could remember the name of the tree drugs correctly.
The same scoring system was used for the symbols
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: nouran t abdelsalam
- Phone Number: +201060122230
- Email: yasser.osman@alexmed.edu.eg
Study Locations
-
-
-
Alexandria, Egypt, 0203
- Recruiting
- Alexandria University
-
Principal Investigator:
- Yasser m osman, assist prof
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- ASA I and II patients
Exclusion Criteria:
- severe or life-threatening condition
- severe visual impairment
- mental or cognitive dysfunction
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: patients receiving the placebo medication
tree different placebo drugs with tree different names and symbols one will be given twice daily one once in the morning one once before bedtime
|
tree different placebo drugs with tree different names and scheduled will be given
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
score for remembering the drug name
Time Frame: memory will be tested after one month from prescribing the drugs
|
A scoring system was used to evaluate patients memory of the drugs name used 0- 3 0 is the minimal score and will be given if no recall of any drug name and 3 is the maximum score and will be given if the patient could remember the name of the tree drugs correctly.
|
memory will be tested after one month from prescribing the drugs
|
|
score for remembering the drug symbol
Time Frame: memory will be tested after one month from prescribing the drugs
|
A scoring system was used to evaluate patients memory of the drugs symbol used 0- 3 0 is the minimal score and will be given if no recall of any drug symbol and 3 is the maximum score and will be given if the patient could remember the symbol of the tree drugs correctly.
|
memory will be tested after one month from prescribing the drugs
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: yasser M osman, Alexandria University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 0305534
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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