A Pilot Study of the VosCryoTM Breathalyser in Lung Cancer (CryoPilot)

July 1, 2026 updated by: Sheffield Teaching Hospitals NHS Foundation Trust

CryoPilot is a single-centre pilot study being conducted at Weston Park Cancer Centre in Sheffield, UK. The goal of this pilot study is to determine whether small-volume exhaled breath condensate sample (EBC) obtained via a VosCryo™ breath sample collection device can provide quantifiable and analysable cellular material, including epithelial cells, leukocytes, or exfoliated tumour cells, in patients with late-stage lung cancer. The main question it aims to answer is whether a breath sample can provide the necessary cellular information that could eventually be used for diagnostic purposes.

The secondary objective is to compare the presence and quality of such material with that obtained from healthy relatives who will act as a low-risk control group, to assess whether EBC-based analysis may differentiate between cancerous and non-cancerous states.

As such this pilot study will have two arms:

  • Experimental arm: 12 patients with late-stage lung cancer
  • Control arm: 12 low-risk relatives of patients with late-stage lung cancer

Participants will be approached during their visit to Weston Park Hospital and asked to provide informed consent, followed by provision of a breath sample.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Detailed Description

Background:

Lung cancer remains one of the leading causes of cancer-related mortality worldwide, with late-stage diagnosis contributing substantially to poor prognosis (Bray et al., 2024). Despite advancements in imaging and molecular diagnostics, early detection strategies remain inadequate for population-wide screening, particularly in resource-limited settings. There is therefore an urgent need for novel, non-invasive, and cost-effective diagnostic approaches suitable for use in at-risk populations, such as individuals with a family history of lung cancer or those with a history of significant exposure to tobacco smoke.

Exhaled breath condensate (EBC) offers a promising, non-invasive source of biomarkers for respiratory diseases including lung cancer (Carpagnano et al., 2005; Palomba et al., 2023). EBC is a biological fluid formed by the cooling of exhaled breath and contains aerosolised droplets from the respiratory tract, including proteins, nucleic acids, volatile organic compounds, and, occasionally, cellular material (Horvath et al., 2005; Mutlu et al., 2001). These components may reflect pathological processes occurring in the lower airways and alveoli, thus offering a window into the disease state without the risks associated with bronchoscopy or biopsy.

Recent technological developments have enabled the reproducible collection of small volumes of EBC in a clinically practical timeframe. The VosCryo™ device, is a commercially available disposable device that collects approximately 100-200 µL of condensate in about one minute. The VosCryo™ which we will use, is a fast, non-invasive, and reliable EBC collector, optimized for small-volume sampling (50-200 µL/min). It is designed for versatile research use - ideal for investigating biomarkers in lung cancer, infectious diseases, or chronic respiratory conditions, with minimal contamination risk and compatible with standard diagnostic assays. Its compact design and ease of use makes it particularly well-suited to clinical and point-of-care environments. Importantly, pilot studies have demonstrated the feasibility of recovering DNA, RNA, and protein from similar volumes of EBC, although the yield and integrity of these components at this low volume remain incompletely characterised (Kharitonov and Barnes, 2006; Phillips et al., 2003).

The aim of this pilot study is to evaluate whether analysable cellular material can be identified within small-volume EBC collected using the VosCryo™ device from patients with advanced lung cancer. This exploratory work will inform the viability of future development of EBC as a low-cost, non-invasive diagnostic in patients with advanced and early-stage lung cancer, and as a potential screening tool for use in at-risk populations. The work has the potential to inform larger-scale biomarker studies and, ultimately, contribute to improved outcomes through earlier diagnosis.

Primary objective:

The primary objective is to determine whether small-volume EBC obtained via VosCryo™ from late-stage lung cancer patients contains quantifiable and analysable cellular material, including epithelial cells, leukocytes, or exfoliated tumour cells.

Secondary objective:

A secondary aim is to compare the presence and quality of such material with that obtained from healthy relatives (acting as a low-risk control group), to assess whether EBC-based analysis may differentiate between cancer and non-cancer states.

Primary Outcome:

The primary outcome is the proportion of participants with lung cancer with analysable material within their exhaled breath condensate.

Secondary Outcome:

The secondary outcome is comparison of exhaled breath condensate from lung cancer patients with participants without lung cancer

Study Design:

This is a pilot study. Potential participants will be approached when attending lung cancer clinics at Weston Park Hospital. Two cohorts of study participants will be recruited:

  1. Patients with previously untreated advanced lung cancer
  2. An accompanying patient friend or relative with no history of lung cancer

Recruitment:

Potential participants will be approached by a Clinical Trials Assistant/Research Nurse when attending lung cancer clinics at Weston Park Hospital. Participants will be provided with the Participant Information Sheet and given time to read this. There will be no minimum time required for this. Participants will be given the chance to discuss the study and ask any questions, then be consented and registered and the EBC research sample collected. Any consenting participants who are unable to complete the research breath sample will be withdrawn. Reasons for sample collection failure will be collected in a screening log.

Patients attending the lung cancer clinic without an accompanying relative can be approached for study participation. Consenting patients with an accompanying relative who declines study participation can be included, as can consenting relatives with a patient who declines. Recruitment will continue until 12 participants have completed the EBC sample collection in both cohorts.

Inclusion criteria:

  • Age ≥16 years old.
  • Signed written consent.
  • Advanced non-small cell or small cell lung cancer with intra-thoracic disease (pulmonary primary or pulmonary metastases), previously untreated by systemic anti-cancer treatment or radiotherapy. Patients with previously treated early-stage lung cancer are permitted. Patients with advanced disease with extra-thoracic disease previously treated by local therapy (e.g. palliative radiotherapy to a bone metastasis, or post brain metastectomy), which in the opinion of the principal investigator is unlikely to impact the quality of the EBC research sample are eligible; or
  • Attending relative or friend with no history of lung cancer or any other primary cancer, except for curatively treated non-melanomatous skin cancer or carcinoma in situ, unless the participant has been free of malignancy and off treatment for a period of at least 2 years prior to study enrolment.
  • No intercurrent upper or lower respiratory tract infection.
  • Able to complete the EBC sample collection.

Exclusion criteria:

  • Participants with lung metastases from non-lung primaries.
  • Participants unable to consent or unable to comply with the requirements for

Study procedures:

Study participants will be allocated a study number. All study data and study research samples will be labelled and recorded using the study number.

All study procedures will be performed at baseline. No follow up procedures are required for this study.

Participant characteristics recorded at baseline:

  • Sex.
  • Age.
  • Smoking status - never smoker, ex-smoker (not smoked >12 months), recent ex-smoker (smoked ≤12 months), current smoker (smoked within past 14 days), vapes.
  • TNM tumour stage 9th edition (where appropriate) from most recent staging scans performed as part of NHS standard of care.
  • Tumour histology (where appropriate) including histological subtype, immunohistochemistry profile, mutation profile and PD-L1 status from results reported as part of NHS standard of care investigations.
  • History of any concurrent pulmonary disease (e.g. emphysema, interstitial lung disease)

Collection of the EBC Research Sample:

The EBC will be collected only once participant informed consent is obtained. The EBC need not be collected on the same visit as consenting but must be collected before starting any anti-cancer treatment.

EBC Research Sample Analysis:

Specimens will be analysed in the School of Bioscience, University of Sheffield, as follows:

  1. The device will be subjected to centrifugation at 90 g for 1 min at ambient temperature using a swing-out rotor.
  2. The total sample volume will be noted.
  3. The supernatant will be removed and stored at -20oC.
  4. Pelleted material will be resuspended in phosphate-buffered saline, and an aliquot dispensed onto a poly-L lysine coated coverslip.
  5. Material will be fixed using 4% paraformaldehyde for 15 minutes and then analysed using immunocytochemistry and indirect immunofluorescence microscopy.
  6. Another aliquot of the pelleted material will be subjected to RNA extraction, cDNA synthesis and qPCR-based analysis of genes expressed in epithelial and immune cell types.
  7. Any remaining samples will be stored at -20oC.
  8. The results will be recorded for data analysis and statistical purposes.
  9. Samples will be stored for the duration of the project (18 months), and may be re-analysed in future prototype versions of this project, and their composition further characterised either by ELISA, fluorescence microscopy or mass spectrometry. After which time, samples will be destroyed by the Chief Investigator.

Statistical Analysis:

12 participants completing the research breath sample will be recruited to each cohort (12 patients with advanced lung cancer, 12 accompanying relatives); i.e. a minimum of 24 participants in total.

Descriptive statistics will be used to summarise and compare the two cohorts.

Study conduct:

The study will be conducted in accordance with the trial protocol, the International Conference on Harmonisation (ICH) for Good Clinical Practice (GCP) and appropriate regulatory requirements. The study will have been approved by the HRA and an NHS Research Ethics Committee prior to commencement.

Recording and reporting of events and incidents:

An Adverse Event (AE) is any untoward medical occurrence in a participant, including occurrences which are not necessarily caused by or related to the intervention.

A serious adverse event (SAE) is any untoward medical occurrence that:

  1. results in death;
  2. is life-threatening;
  3. requires hospitalisation or prolongation of existing hospitalisation;
  4. results in persistent or significant disability or incapacity; or
  5. consists of a congenital abnormality or birth defect; or
  6. is otherwise considered medically significant by the investigator. NOTE: The term "life-threatening" in the definition of "serious" refers to an event in which the participant was at risk of death at the time of the event; it does not refer to an event which hypothetically might have caused death if it were more severe.

The research device is single use and the procedure to collect the EBC research sample does not require any period of extended restricted breathing, hyperventilation or forced breathing. With no increased work of breathing, there are no expected adverse or serious adverse events (SAEs) from study participation.

In the unlikely event of any SAE occurring, these will be managed as per local standard practise. Any SAEs that are related to the trial (i.e., they result from administration of any of the research procedures) and unexpected (i.e., not listed in the protocol as an expected occurrence) will be emailed to the research ethics committee (REC) using the non-CTIMP safety report to REC form. These will be sent within 15 days of the chief investigator becoming aware of the event.

Data Handling:

Consenting participants will be assigned a study number. This number will be used to label the research sample and participant study data. No participant personal identifiers will be stored.

Project Timescales:

It is estimated that participant recruitment and sample collection will be completed over a 6-month period, with subsequent sample and data analysis completing over an additional 12-month period. A final study report will then be generated.

Funding Arrangements:

This project is funded by VosBio (the manufactures of the VosCryo™ device). The University of Sheffield will be the fundholder and any NHS funds will be paid upon submission of invoices as per the study contract.

Study Type

Observational

Enrollment (Estimated)

24

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

The study population will consist of two cohorts of participants:

  • Patients with previously untreated advanced lung cancer, who meet the relevant inclusion criteria and are under treatment at or have been referred to Weston Park Hospital
  • Friends or relatives with no history of lung cancer, who are accompanying a patient with advanced lung cancer to Weston Park Hospital

Description

Inclusion Criteria:

  • Age ≥16 years old
  • Ability to provide written informed consent

  • Either a history of advanced non-small cell or small cell lung cancer with intra-thoracic disease (pulmonary primary or pulmonary metastases), previously untreated by systemic anti-cancer treatment or radiotherapy

    • Patients with previously treated early-stage lung cancer are permitted
    • Patients with advanced disease with extra-thoracic disease previously treated by local therapy (e.g., palliative radiotherapy to a bone metastasis, or post brain metastectomy), which in the opinion of the Principal Investigator is unlikely to impact the quality of the EBC research sample are eligible
  • OR an attending relative or friend with no history of lung cancer or any other primary cancer, except for curatively treated non-melanomatous skin cancer or carcinoma in situ, unless the participant has been free of malignancy and off treatment for a period of at least 2 years prior to study enrolment
  • No intercurrent upper or lower respiratory tract infection
  • Able to complete the EBC sample collection

Exclusion Criteria:

  • Participants with lung metastases from non-lung primary tumours
  • Participants unable to consent or unable to comply with the requirements for EBC sample collection

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Experimental Arm
Patients with advanced/late-stage lung cancer
Other: Expiratory Breath Condensate Collection
Collection of Expiratory Breath Condensate using the VosCryo device
Control Arm
Relatives of advanced lung cancer patients, at low risk of/with no known malignancy.
Other: Expiratory Breath Condensate Collection
Collection of Expiratory Breath Condensate using the VosCryo device

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Availability of Analysable Sample Material
Time Frame: At Collection of EBC Sample
The number of participants with lung cancer out of the total recruited to the experimental arm, who have analysable material within their exhaled breath condensate.
At Collection of EBC Sample

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cross-Cohort Sample Discrepancy
Time Frame: Variation in gene expression identified at end of study, from samples collected at baseline visit.
Variation in gene expression in epithelial and immune cells between advanced lung cancer patients and healthy controls, as demonstrated by RNA extraction, cDNA synthesis and qPCR-based analysis of EBC samples.
Variation in gene expression identified at end of study, from samples collected at baseline visit.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sheffield Teaching Hospitals NHS Foundation Trust

Collaborators

University of Sheffield

Investigators

  • Principal Investigator: Robin J Young, MBChB MRCP PhD, Sheffield Teaching Hospitals NHS Foundation Trust

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

September 1, 2026

Primary Completion (Estimated)

February 1, 2027

Study Completion (Estimated)

February 1, 2028

Study Registration Dates

First Submitted

July 1, 2026

First Submitted That Met QC Criteria

July 1, 2026

First Posted (Actual)

July 8, 2026

Study Record Updates

Last Update Posted (Actual)

July 8, 2026

Last Update Submitted That Met QC Criteria

July 1, 2026

Last Verified

July 1, 2026

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • STH23461
  • IRAS (Other Identifier: 361767)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

For protection of participants, raw individual participant data will not be distributed outside of the immediate research team. Pseudonymised individual data will be transferred to partnering organisations (e.g., University of Sheffield) for data analysis purposes, and overall findings will be relayed to participants and may be publicised in academic journals/conferences, however IPD will be retained by the immediate study team.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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