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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05677776
Other study ID # 2021-98
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 1, 2021
Est. completion date December 30, 2022

Study information

Verified date February 2023
Source Erol Olcok Corum Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

It is aimed to examine the retrospective features of covid-19 patients followed in our hospital with pneumothorax.


Description:

It is aimed to examine the retrospective features of covid-19 patients followed in our hospital with pneumothorax. The files of covid-19 patients with pneumothorax were reviewed retrospectively. The radiological records and treatment protocols of the patients were reviewed. The results were evaluated in terms of its relationship with pneumothorax.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date December 30, 2022
Est. primary completion date December 10, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - over 18 years - covid-19 patient - having a diagnosis of pneumothorax - PCR test positive and lung tomography pneumonic involvement Exclusion Criteria: - PCR test negative

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Turkey Hulya TOPCU Çorum

Sponsors (1)

Lead Sponsor Collaborator
Erol Olcok Corum Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary relationship between covid-19 and pneumothorax Inflammatory markers, C-reactive protein (CRP), lactate dehydrogenase (LDH), ferritin, D-dimer, procalcitonin, blood gas lactate, creatine kinase, white blood cells, baseline laboratory test results including WBC, lymphocyte, neutrophil counts, platelets, urea, creatinine, and neutrophil/lymphocyte ratio were documented for each patient.
Respiratory support status, the fraction of inspired oxygen (FiO2), positive end-expiratory pressure (PEEP) values, tidal volume, and duration of the mechanical ventilator (MV) stay were determined.
1 year
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