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Clinical Trials/NCT04690920
NCT04690920CompletedNot Applicable

Theranostic Implication of Complimentary Medicines Against IL-6/Gp-130 in COVID-19.: An in Vitro and in Silco Approach

University of Lahore1 site in 1 country200 target enrollmentStarted: July 23, 2020Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
200
Locations
1
Primary Endpoint
Ratio of partial pressure of oxygen in arterial blood to fraction of inhaled oxygen

Study Overview

Brief Summary

IL-6 is an inflammatory marker, secrete by the cells in many pathological conditions like COVID-19 pneumonia. Interleukin 6 bind with its receptors (IL-6R) on cells surface and recruited a protein for its activation known as gp-130. Activated receptors send signals to nucleus through secondary messenger system and up regulate the expression of IL-6/GP130 domain. Total of two hundred (n=200) participants were included in the current study and divided equally in four groups. Group B is given Tocilizumab and Group C is treated with Remdesivir along with the approved standard treatment. Group D is only Given standard therapy and Group A constituted normal healthy age and sexed matched participants. Levels of gp-130 were estimated by commercially available ELISA kit. To estimate the relationship of severity of disease with gp-130 and IL-6 Pearson's correlations was used. Sensitivity and specificity for what purpose

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Admitted diagnosed cases of COVID-19 infection on real time polymerase chain reaction (RT-PCR) Both male and female were included All participants were on oxygen therapy

Exclusion Criteria

  • Asthmatics pulmonary fibrosis chronic obstructive pulmonary disease (COPD) Allergic to remdesivir Allergic to Actemra Refused to take consent

Arms & Interventions

Tocilizumab

Experimental

Intervention: Tocilizumab (Drug)

Remdesivir

Experimental

Intervention: Tocilizumab (Drug)

Standard Treatment

Active Comparator

Intervention: Tocilizumab (Drug)

Outcomes

Primary Outcomes

Ratio of partial pressure of oxygen in arterial blood to fraction of inhaled oxygen

Time Frame: 7 days

Secondary Outcomes

  • Hospital stay(15 days)
  • Viral load(7-15 days)
  • Oxygen demand(7-15 days)

Investigators

Sponsor
University of Lahore
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dr Muhammad Mansoor Hafeez

Doctor

University of Lahore

Study Sites (1)

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