Information:
Fel:
ID
34422
Beskrivning
Powered Echelon Device in VATS Surgery; ODM derived from: https://clinicaltrials.gov/show/NCT01808430
Länk
https://clinicaltrials.gov/show/NCT01808430
Nyckelord
Versioner (1)
- 2019-01-17 2019-01-17 -
Rättsinnehavare
GSK group of companies
Uppladdad den
17 januari 2019
DOI
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Licens
Creative Commons BY-NC 3.0
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Eligibility Non-small Cell Lung Cancer (NSCLC) NCT01808430
Eligibility Non-small Cell Lung Cancer (NSCLC) NCT01808430
- StudyEvent: Eligibility
Similar models
Eligibility Non-small Cell Lung Cancer (NSCLC) NCT01808430
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
ID.1
Item
histologically confirmed nsclc (up to and including stage ii) for patients undergoing vats lobectomy. for patients undergoing wedge resection for undiagnosed pulmonary nodule or metastasis from crc, a malignant diagnosis may be confirmed post-operatively.
boolean
ID.2
Item
scheduled for lung resection surgery (lobectomy or wedge resection) involving only one lobe of the lung
boolean
ID.3
Item
willing to give consent and comply with evaluation and treatment schedule
boolean
ID.4
Item
at least 18 years of age
boolean
ID.5
Item
active bacterial infection or fungal infection
boolean
ID.6
Item
systemic administration (intravenous or oral) of steroids (within 30 days prior to study procedure)
boolean
ID.7
Item
chemotherapy or radiation therapy for lung cancer may not be performed for 30 days prior to the procedure
boolean
ID.8
Item
scheduled concurrent surgical procedure other than wedge resection or lobectomy (central venous access - e.g. port placement, mediastinoscopy with lymph node sampling, and vats lymphadenectomy are allowed);
boolean
ID.9
Item
prior history of vats or open lung surgery
boolean