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NCT03383497 Clinical Trial

The Clinical Profile of Parkinson Disease in Egypt

Parkinson's Disease Clinical Trial

Official title:
The Clinical Profile of Parkinson Disease in Egypt: A Retrospective Cohort Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03383497
Other study ID # CU 816
Secondary ID
Status Completed
Phase N/A
First received September 12, 2016
Last updated December 19, 2017
Start date May 2016
Est. completion date December 2016

Study information
Verified date December 2017
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Multi-center, retrospective observational cohort study in 4 tertiary referral centers in Cairo over the period from 2004 to 2016.

Study population. including all patients with idiopathic Parkinson disease attending. Patients were diagnosed in accordance to the United Kingdom - Parkinson Disease Society Brain Bank criteria.

Description:

Retrospective, observational study that involve Medical Record Review (MRR). Data extraction and collection from medical records was organized through an electronic structured data collection form by two of authors (H.S and N.S).

The abstraction documents included; patient's age, sex, family history, age at onset, type and side of motor symptoms onset, associated non-motor manifestations. Moreover; management plan, drug history, outcome and disease progression were also verified and recorded.

During medical record reviewing (MRR); any missing documentation or poorly recorded information was managed by deleting the case.

Recruitment information / eligibility
Status Completed
Enrollment 1237
Est. completion date December 2016
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender All
Age group 25 Years to 85 Years
Eligibility Inclusion Criteria:

- All patients with Parkinsonian syndromes

Exclusion Criteria:

- Records with missing operationalized variables from patient records

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Cairo University

Outcome
Type Measure Description Time frame Safety issue
Primary time to L-Dopa start The time to L-Dopa start from symptoms onset in relation to time of Diagnosis 6 - 12 months
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