Skip to content

Efficacy Assessment of CT-guided Hook Wire Localization of Lung Nodes Before Thoracoscopy

Efficacy Assessment of CT-guided Hook Wire Localization of Lung Nodes With Medical Device Fil d'Ariane Laurane médical Before Thoracoscopy- HARNO Trial

Status
Withdrawn
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02648594
Acronym
HARNO
Enrollment
0
Registered
2016-01-07
Start date
2016-10-31
Completion date
2017-05-31
Last updated
2018-01-24

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

Conditions

Nodes, Lung

Keywords

lung, thoracoscopy, hook wire localization

Brief summary

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.

Detailed description

For lung cancer patients, the best treatment remains the surgery when tumor is localized. 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. In France, only 1% of surgeries qu'en France, thoracoscopy represents less than 1% of lung cancer surgeries while it represents 30% of interventions in Japan. Moreover, this technic needs that nodes was well localized. For this, radiologists use CT-guided hook wire localization of these lung nodes before surgery. According to the litterature, this localization technic is efficient (Chen et al, 2011). The 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. This implies that: * the hook wire was well CT-guided in the lung * the hook wire did not present a dislodgment before or during surgery * the hook wire is near of the node to be removed Among secondaries objectives, the investigators will assess the safety and possible complications which could occur. The investigators will also measure the distance between hook wire and center of the node

Interventions

DEVICEHook wire CT guided

The intervention consist to place a CT-guided hook wire in lung patient

Sponsors

Centre Jean Perrin
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Nodule detection in surgery piece (success rate)At surgery

Secondary

MeasureTime frame
Nodule detection under scannerAfter patient inclusion, at scan realisation, before surgery. This detection will be realised up to 4 weeks after inclusion.
Adverse events assessment graded with NCI -CTCAE v4.0Before and after surgery, up to 4 weeks after surgery

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026