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Clinical Trials/NCT02648594
NCT02648594
Withdrawn
Phase 2

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

Centre Jean Perrin1 site in 1 countryOctober 2016
ConditionsNodes, Lung

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Nodes, Lung
Sponsor
Centre Jean Perrin
Locations
1
Primary Endpoint
Nodule detection in surgery piece (success rate)
Status
Withdrawn
Last Updated
8 years ago

Overview

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

Registry
clinicaltrials.gov
Start Date
October 2016
End Date
May 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Centre Jean Perrin
Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Nodule detection in surgery piece (success rate)

Time Frame: At surgery

Secondary Outcomes

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

Study Sites (1)

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