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Clinical Trials/NCT04945811
NCT04945811
Completed
Not Applicable

Role of Interleukin-6 and Procalcitonin in Evaluating COVID 19 Disease Severity - an Experience at CMH Quetta

FARAH AFZAL1 site in 1 country100 target enrollmentApril 1, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Covid19 Positive Patients
Sponsor
FARAH AFZAL
Enrollment
100
Locations
1
Primary Endpoint
Levels of inflammatory biomarkers is raised in accordance with severity of COVID 19
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Serum Interleukin-6 and Procalcitonin of 100 consenting COVID 19 positive patients from April 2020 - May 2021 were assessed at Pathology department CMH Quetta and the results were correlated with severity of lung involvement on HRCT Chest

Detailed Description

Objective: To explore the relation between Interleukin-6 and Procalcitonin with COVID severity on HRCT Chest Study Design: Randomized Control Trial (Clinical Trials. gov Identifier: NCT04798391) Place and duration of study: Pathology, Radiology \& ENT Department CMH Quetta from April 2020 - May 2021 Methodology: Serum Interleukin-6 and Procalcitonin of 100 consenting COVID 19 positive patients from April 2020 - May 2021 were assessed at Pathology department CMH Quetta and the results were correlated with severity of lung involvement on HRCT Chest Results: Serum Interlukin-6 levels were raised in 97 (97%) patients with mean levels of 20.43 + 19.66 (pg/ml). Serum procalcitonin levels were raised in 95 (95%) patients with mean levels of 0.4331 + 0.24 (ng/ml). A P value of \<0.001 was calculated on Independent Sample T-test for both serum interlukin-6 and serum procalcitonin as correlated with severity of lung involvement on HRCT Chest. Conclusion: Interlukin-6 and procalcitonin are excellent biomarkers for diagnosis and predicting severity of COVID19 pneumonia. Keywords: Covid19 pneumonia, Interlukin-6, procalcitonin.

Registry
clinicaltrials.gov
Start Date
April 1, 2020
End Date
May 30, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
FARAH AFZAL
Responsible Party
Sponsor Investigator
Principal Investigator

FARAH AFZAL

CLASSIFIED SPECIALIST

Combined Military Hospital, Pakistan

Eligibility Criteria

Inclusion Criteria

  • positive PCR of COVID 19

Exclusion Criteria

  • NEGATIVE PCR of COVID 19

Outcomes

Primary Outcomes

Levels of inflammatory biomarkers is raised in accordance with severity of COVID 19

Time Frame: 2 days

serum Interlukin-6 levels was measured on COBAS-e 411 Immunoassay analyzer using electro chemiluminescence methodology using Roche Interlukin-6 kit with raised levels taken as \> 7 pico gram / milliliter (pg/ml). Serum procalcitonin were also measured by similar methodology using Roche procalcitonin kit with raised levels taken as \> 0.15 nano gram / milliliter (ng/ml). COVID 19 pneumonia was categorized on HRCT chest as Mild with total score 7 or less, moderate with score from 8 - 17, and severe with score more than 18.

Study Sites (1)

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