COVID-19 and Rhino-orbital Mucormycosis
Sponsor
Minia University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05212961
Collaborator
(none)
40
1
9.6
4.2
Study Details
Study Description
Brief Summary
Detect the clinical presentation and outcome of post covid-19 fungal mucormycosis in patients referred to Minia university Hospital.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Study Design
Study Type:
Observational
Anticipated Enrollment
:
40 participants
Observational Model:
Case-Only
Time Perspective:
Retrospective
Official Title:
Clinical Profile and Outcome of Post Covid-19 Rhino-orbital Fungal Mucormycosis in Minia Governorate
Actual Study Start Date
:
Dec 28, 2021
Anticipated Primary Completion Date
:
Sep 28, 2022
Anticipated Study Completion Date
:
Oct 15, 2022
Outcome Measures
Primary Outcome Measures
- Outcome of rhino-orbital mucormycosis in COVID-19 patients [9 months]
Data of the patients who had post Covid-19 fungal mucormycosis in the last year will be revised to detect clinical presentation and final outcome
Eligibility Criteria
Criteria
Ages Eligible for Study:
N/A
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
-
Patients who had positive PCR test for Covid-19.
-
Fungal rhino-orbital infection was confirmed.
Exclusion Criteria:
-
Suspected patient with COVID-19 not confirmed with PCR
-
Incomplete data
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Faculty of Medicine- Minia University | Minya | Egypt | 61111 |
Sponsors and Collaborators
- Minia University
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Sahar T A Abdelaziz,
Assistant Professor,
Minia University
ClinicalTrials.gov Identifier:
NCT05212961
Other Study ID Numbers:
- Ophthalmology
First Posted:
Jan 28, 2022
Last Update Posted:
Aug 8, 2022
Last Verified:
Aug 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms: