Nodes, Lung Clinical Trial
— HARNOOfficial title:
Efficacy Assessment of CT-guided Hook Wire Localization of Lung Nodes With Medical Device " Fil d'Ariane " Laurane médical Before Thoracoscopy- HARNO Trial
Verified date | January 2018 |
Source | Centre Jean Perrin |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
When patient presents a lung node, there is an important risk that this node was a tumor. For
patients who have these nodes, the surgery is the best treatment. When the surgery is
possible, the thoracoscopy may be more advantageous compared to thoracothomy (decrease of
post surgery pains, decrease of recovery time and decrease of drugs consumption).
Nevertheless, thoracoscopy needs specific materiels and nécessite un équipement spécifique
and trained physicians.
Moreover, this technic needs that nodes was well localized. For this, radiologists use
CT-guided hook wire localization of these lung nodes before surgery.
TThe hook wire laying is delicate. It can lead secondaries effects as pneumothorax,
dislodgement of the hook wire before and after surgery. The success rate of hook wire
fixation in lung near of the node is primary.
The main objective of our study is to assess the success rate localization of node in surgery
piece, that is to verify if the hook wire have allowed to localize the lung node in surgery
piece.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | May 2017 |
Est. primary completion date | May 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Age > 18 years - Patient with suspect lung node, needed surgery - Signed consent Exclusion Criteria: - Too deep node - Severe co-morbidities : respiratory insufficiency, cardiac insufficiency - Major emphysema - Patient with only one lung - Pregnant women - Breastfeeding women - Patient with cognitive and psychiatric troubles |
Country | Name | City | State |
---|---|---|---|
France | Centre Jean Perrin | Clermont-Ferrand |
Lead Sponsor | Collaborator |
---|---|
Centre Jean Perrin |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Nodule detection in surgery piece (success rate) | At surgery | ||
Secondary | Nodule detection under scanner | After patient inclusion, at scan realisation, before surgery. This detection will be realised up to 4 weeks after inclusion. | ||
Secondary | Adverse events assessment graded with NCI -CTCAE v4.0 | Before and after surgery, up to 4 weeks after surgery |
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