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CompletedNCT04690920Updated Dec 31, 2020

Theranostic Implication of Complementary Medicines Against Interleukin Receptors and Gp-130 Proteins

An interventional study of Tocilizumab in Corona Virus Disease 2019 (COVID-19), sponsored by University of Lahore. Completed at 1 site in Pakistan. Per ClinicalTrials.gov, last updated 2020-12-31.

Sponsored by University of Lahore · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 4 months after the study started (first participant enrolled Jul 2020, registered Dec 2020).
Phase
Not applicable
Study type
Interventional
Enrollment
200
Allocation
Randomized
Sex
All
01

Study 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

02

Conditions studied

  • Corona Virus Disease 2019 (COVID-19)

Keywords

  • corona virus disease 2019 (COVID-19)
  • Tocilizumab
  • Remdesivir
  • Interleukin receptor-6, glycoprotein-130
  • receptor blocker
03

In context

COVID-19

7,640 studies on the registry are indexed under COVID-19; 488 are open to participants now.

This study's enrollment of 200 is above the median of 100 across 4,099 interventional studies indexed under COVID-19.

Browse COVID-19 studies →

Lead sponsor

University of Lahore is the lead sponsor of 223 studies on the registry; 40 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
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

Exclusion Criteria:

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

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
200 participants (actual)

Study arms

  • No intervention
    Control
  • Experimental
    Tocilizumab

    Drug: Tocilizumab

  • Experimental
    Remdesivir

    Drug: Tocilizumab

  • Active comparator
    Standard Treatment

    Drug: Tocilizumab

Interventions

  • DrugTocilizumab

    Comparison of drugs, Tocilizumab, Remdesivir, standard treatment with controls

    Also known as: Remdesivir, Standard treatment with Antibiotic, oxygen, Vitamin C, Statins, No treatment is given to control group

06

What researchers measure

Primary outcomes

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

    Time frame: 7 days

Secondary outcomes

  1. Hospital stay

    Time frame: 15 days

  2. Oxygen demand

    Time frame: 7-15 days

  3. Viral load

    by RT-PCR

    Time frame: 7-15 days

07

Study locations

1 site
  • The University of Lahore
    Lahore, Punjab 54000, Pakistan
08

References and documents

Individual participant data

Plan to share: Undecided — statistical analysis, results

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 31, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04690920
Lead sponsor
University of Lahore
Responsible party
Dr Muhammad Mansoor Hafeez (Doctor, University of Lahore) — Principal investigator
First posted
Dec 31, 2020
Start date
Jul 23, 2020
Primary completion
Dec 10, 2020
Completion
Dec 10, 2020
Last update
Dec 31, 2020

Study contacts

Arif Malik, PhD
study director · The University of Lahore

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2020. You cannot join it, but the record below documents what was studied.

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