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Self-Collected Nasal swab, Throat swab, and Finger Prick Blood for detection of COVID-19 infection

Self-Sample Collection and Transportation for detection of SARS-CoV-2 presence using RT-PCR and Antibody Testing Mechanism

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/05/033721
Enrollment
240
Registered
2021-05-21
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

None listed

Interventions

None listed

Sponsors

ACES ECOSPHERE LLP
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participant older than 18 with symptoms or recently been in contact with COVID-19 positive patient (High-Risk Individual) and present for COVID-19 testing in OPD, and able to understand and follow instructions for self-collection. OR Participant recently infected with COVID-19 and quarantined in the institutional quarantine center with individual room and home-like atmosphere. Participant able to understand the instructions i.e. read, write and speak in any one language i.e. English, Hindi, and Marathi Participant for unsupervised self-sample collection should have own fridge for freezing ice gel packs

Exclusion criteria

Exclusion criteria: Unable or unwilling to provide informed consent and /or reliable contact information. Participant unable to read and write in English, Hindi, or Marathi Younger than 16 and older than 65 are not eligible for this study. No fridge or active internet connection for at-home sample collection.

Design outcomes

Primary

MeasureTime frame
To investigate the reliability and evaluate the performance of self-sample collection and transportation, healthcare workers will also extract the sample of subjects and the results will be compared to understand the quality of at-home unsupervised self-collected sample. The methods will be further compared with end result outcomes i.e. +ve or -ve. The match on the end result will provide an inference that the self-sample collection and transportation is feasible testing mechanism.Timepoint: 2 to 4 weeks

Secondary

MeasureTime frame
The objective of the proposed research is to test a reliable diagnostic system that will enable participant to self-administer and collect their own samples with the help of an instruction manual. Participants will collect both nasopharyngeal and oropharyngeal samples for RT-PCR testing and dried blood spot sample for antibody testing.Timepoint: 2 to 4 weeks

Countries

India

Contacts

Public ContactSitanshu Shastri

Government Medical College and Hospital

drswatimbhise@gmail.com

Outcome results

None listed

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