- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05839249
The Impact of Covid 19 Pandemic on Ureteric Stents Complications.
Study Overview
Status
Intervention / Treatment
Detailed Description
Type of the study: retrospective clinical study
Study Setting: Qena University Hospital 3- Study subjects:
a. Inclusion criteria: all patients performing JJ stent placement during Covid 19 pandemics b. Exclusion criteria: Patients refuse to participate in this study c. Sample Size Calculation: all patients performing JJ stent placement from March 2020 to December 2021
Study tools (in detail, e.g., lab methods, instruments, steps, chemicals, …):
- Medical history
- Complete physical examination.
All patents presented was investigated by
- Abdominal U.S
- Plain X Ray
- Non contrast CT
- Serum Creatinine
- Urine Analysis
Research outcome measures:
- Primary (main): determine effect of urological malpractice during Covid 19 on patient complications
- Secondary (subsidiary): determine JJ stent complications during Covid 19 pandemics
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Qina
-
Qinā, Qina, Egypt, 831115
- South Valley University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- all patients performing JJ stent placement during Covid 19 pandemics
Exclusion Criteria:
- Patients refuse to participate in this study
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
jj stents complications during covid 19 pandimics
Time Frame: 3 years
|
determine effect of urological malpractice during Covid 19 on patient complications
|
3 years
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- SVU/MED/URO016/2.23.4.539
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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