Skip to content

Data Analysis of THINQURE 20 in COVID 19 Patients

A Non-Interventional, Retrospective, Observational Study to Analyze Safety, Efficacy and Tolerability of THINQURE 20 in COVID-19 Patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/03/032471
Enrollment
25
Registered
2021-03-31
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere

Interventions

None listed

Sponsors

Thinq Pharma CRO Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: We will consider the following criteria for retrospective analysis. 1. Male or Female subjects of age 18 to 75 years (both inclusive). 2. Subjects diagnosed with COVID-19 by RT-PCR. 3. Patients provided oral & nasal swabs for test 4. Females of child-bearing potential (i.e., who were not chemically or surgically sterilized or who were not post-menopause) must have had a negative urine pregnancy test. 5. Females of child-bearing potential who have used a medically accepted method of contraception that was considered reliable in the judgment of the investigator. 6. Subjects who have taken Thinqure 20 as prescribed by Investigator.

Exclusion criteria

Exclusion criteria: Subjects were excluded on the following basis: 1. Patients with a history of intracranial bleeding 2. Patients without a completed medical history 3. Patients, who were suffering from any haemoglobinopathies such as thalassemia that could interfere with oxygen carriage in the blood. 4. Patients, who were smokers or consumed alcohol. 5. Patients, who were suffering from active malignancy along with squamous cell or basal cell skin cancer. 6. Female subjects who were pregnant or lactating or planning to become pregnant during the study period. 7. Females who were not ready to use acceptable contraceptive methods during the course of study.

Design outcomes

Primary

MeasureTime frame
Reduction in viral load from baseline to end of study visit.Timepoint: Day 1 to Day 5

Secondary

MeasureTime frame
The assessment of safety and tolerability of Investigational Product.Timepoint: Day 1 to Day 5

Countries

India

Contacts

Public ContactDr Milind Gharpure

Mediclin Clinical Research

ravindra.mote@mediclincr.com8888884024

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026