Changing of Prostate Specific Antigen Value in Patients With Covid-19

Sponsor
Saglik Bilimleri Universitesi (Other)
Overall Status
Recruiting
CT.gov ID
NCT05009186
Collaborator
(none)
100
1
1
18
5.6

Study Details

Study Description

Brief Summary

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) caused a worldwide pandemic in over 100 years. The disease caused by this newly discovered virus was called Covid-19. In this study, we aimed to evaluate changing of PSA value in patients with Covid-19.

Condition or Disease Intervention/Treatment Phase
  • Other: PSA value
N/A

Detailed Description

Patients with positive PCR test results were included in the study. The age of the patient and urea, leukocyte, hemoglobin, platelet, urea, and creatinine values of the patients were recorded. Urinalysis and urine culture were taken from all patients. Acute phase reactants such as sedimentation, C-reaktif protein (CRP), ferritin, and fibrinogen were measured both at the time the patients applied and three weeks after the patient recovered. PSA and free PSA were also measured in the same way. Patients whose symptoms improved and the PCR test result was negative were considered as recovered.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
We measured PSA value during and after Covid-19 infectionWe measured PSA value during and after Covid-19 infection
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Changing of PSA With Covid-19
Actual Study Start Date :
Apr 1, 2020
Anticipated Primary Completion Date :
Oct 1, 2021
Anticipated Study Completion Date :
Oct 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Other: Covid-19 group

We will measure the PSA value during and after Covid-19 infection in the same group via paired simple t test

Other: PSA value
We measure PSA value during and after covid-19 infection

Outcome Measures

Primary Outcome Measures

  1. PSA value [2 months]

    prostate specific antigen

Secondary Outcome Measures

  1. Ferritin, CRP [2 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
45 Years to 70 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Male patients (>45 and <70 years of age) positive PCR test results were included in the study
Exclusion Criteria:
  • The patients <45 and >70 years of age who described lower urinary tract symptoms who had urinary tract infection who a history of prostate biopsy and previous high level of PSA who history of prostatitis were excluded.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Omer Gokhan Doluoglu Ankara Altindag Turkey 06100

Sponsors and Collaborators

  • Saglik Bilimleri Universitesi

Investigators

  • Principal Investigator: Omer G Doluoglu, Associate Professor, Ankara Training and Research Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Omer Gokhan Doluoglu, Ankara Training and Research Hospital, Saglik Bilimleri Universitesi
ClinicalTrials.gov Identifier:
NCT05009186
Other Study ID Numbers:
  • PSA
First Posted:
Aug 17, 2021
Last Update Posted:
Aug 17, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Omer Gokhan Doluoglu, Ankara Training and Research Hospital, Saglik Bilimleri Universitesi
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 17, 2021