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NCT07401797Toboroz

Specimens for Lung Cancer Panel Design

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. febr. 10.

Rövid összefoglaló (regiszter, angolul)

This is an observational study designed to determine the optimal combination of biomarkers and clinical data for the early detection, confirmation, and better treatment of lung cancer including minimizing recurrence.

Állapot (regiszter)
Toboroz
Vizsgálattípus
Megfigyeléses
Résztvevők száma
2000 (tervezett)
Első benyújtás
2026. febr. 3.
Kezdés
2024. aug. 7.
Elsődleges befejezés
2029. dec. 31.
Fő szponzor
Maverix Medical
Betegségek
Tüdőrák
NCT-szám
NCT07401797

Mit vállalsz

  • Vizsgálat típusa: Megfigyeléses
  • Tervezett résztvevők: 2000
  • 2024. aug. 7. és az elsődleges befejezés (2029. dec. 31.) között
  • 1 helyszín, 1 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

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A regiszterben nem jelölt feltételek

  • 6.1 Criteria for the no prior cancer suspicious nodule arm
  • Inclusion:
  • The patient has at least one indeterminant nodule with a diameter greater than or equal to 5mm and a Mayo SPN risk greater than 5%, identified by radiology, that has not been biopsied or undergone surgery.
  • The patient and the treating physician intend to follow up on the nodule with a biopsy procedure, PET scan, or active surveillance, with the procedure or next surveillance planned within the next 7 months.
  • Ability to understand the study and sign an informed consent form
  • Relevant clinical data accessible
  • Ability and willingness to safely donate 40 mL of blood
  • Ability of the site to collect and process blood per protocol Exclusion
    • 1\. The patient has one or more nodules with a Mayo SPN risk over 50% or a diameter of 30mm or greater.
    • 2\. The patient has received surgical prep, including antibiotics, anesthesia, etc. Fasting is not exclusionary.
    • 3\. Previous cancer diagnosis of any origin. 4. Is currently pregnant 5. Is currently a prisoner or becomes a prisoner at any point during the study 6. Is under age 18, is unable to consent, or requires a different person or entity to consent on their behalf 6.2 Criteria for the previous cancer suspicious nodule arm
    • Inclusion:
    • 1\. The patient has at least one indeterminant nodule with a diameter greater than or equal to 5mm and a Mayo SPN risk greater than 5%, identified by radiology, that has not been biopsied or undergone surgery.
    • 2\. The patient and the treating physician intend to follow up on the nodule with a biopsy procedure, PET scan, or active surveillance, with the procedure or next surveillance planned within the next 7 months.
    • 3\. The patient has been in remission for a previous cancer not of lung origin for more than 5 years.
    • 4\. Ability to understand the study and sign an informed consent form 5. Relevant clinical data accessible 6. Ability and willingness to safely donate 40 mL of blood 7. Ability of the site to collect and process blood per protocol Exclusion
  • The patient has one or more nodules with a Mayo SPN risk over 50% or a diameter of 30mm or greater.
  • The patient has received surgical prep, including antibiotics, anesthesia, etc. Fasting is not exclusionary.
  • Previous cancer diagnosis in the lung (either of lung origin or metastasis to the lung).
  • The treating physician believes the lung nodule is a recurrence of a previously diagnosed cancer.
  • Is currently pregnant
  • Is currently a prisoner or becomes a prisoner at any point during the study
  • Is under age 18, is unable to consent, or requires a different person or entity to consent on their behalf
    • 6.3 Criteria for the healthy volunteer arm
    • Inclusion:
  • Ability to understand the study and sign an informed consent form
  • Relevant clinical data accessible
  • Ability and willingness to safely donate up to 40 mL of blood
  • The ability of the site to collect and process blood per protocol Exclusion
    • 1\. Is currently pregnant 2. Is currently a prisoner or becomes a prisoner at any point during the study 3. Is under age 18, is unable to consent, or requires a different person or entity to consent on their behalf

Életkor a regiszterben: 18 év – - · Nem: nők és férfiak · Egészséges önkénteseket is fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (1)

Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.

HelyszínVárosOrszágHelyszín állapota
Maverix Medical
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PhoenixEgyesült ÁllamokToboroz

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