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Identifying and investigating abnormal areas on the lung using UV light

Not Applicable
Suspended
Conditions
Primary spontaneous pneumothorax
Respiratory
Pneumothorax
Registration Number
ISRCTN14196090
Lead Sponsor
niversity of Oxford
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Suspended
Sex
All
Target Recruitment
28
Inclusion Criteria

1. Patient undergoing Video-assisted Thoracoscopic Surgery (VATS) for pneumothorax recurrence prevention, or ongoing air leak (pneumothorax group) OR Thoracic surgery for another indication, for example, early-stage lung cancer or metastasis resection (control group).
2. Male or female aged between 16 and 55 years (inclusive)

Exclusion Criteria

1. Inability to consent or comply with the trial requirements
2. Patients in the control group should not have demonstrable emphysema (on CT scanning) and should not have experienced a spontaneous pneumothorax in the past
3. Allergy to fluorescein
4. Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the study, or may influence the result of the trial, or the participant’s ability to participate in the study

Study & Design

Study Type
Other
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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