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Smellprints in lung Cancer; the role of ENose in diagnosis and Treatment (SCENT): part 3. Acute effects on smellprints of chemotherapy in patients with lung cancer.

Smellprints in lung Cancer; the role of ENose in diagnosis and Treatment (SCENT): part 3. Acute effects on smellprints of chemotherapy in patients with lung cancer. - SCENT study, part 3

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON32493
Enrollment
75
Registered
2008-12-30
Start date
2009-01-26
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

lung cancer or bronchial carcinoma

Interventions

first cycle of chemotherapy for lung cancer. Patients were already scheduled for this treatment after staging work-up. NSCLC: cisplatin/gemcitabin SCLC: cisplatin/etoposide

Sponsors

Medisch Centrum Leeuwarden
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: -Informed consent is obtained. -newly diagnosed adenocarcinoma or squamous cell carcinoma stage IIIA, IIIB or IV or small cell lung cancer) -Adults 18-80 years. -scheduled for chemotherapy as first part of the treatment: Cisplatin/Gemcitabine (NSCLC) and Cisplatin/Etoposide (SCLC)

Exclusion criteria

Exclusion criteria: -Previous chemotherapy -unable to evaluate response with the RECIST criteria. -unable to follow the instructions for the eNose measurement -eating, drinking and smoking

Design outcomes

Primary

MeasureTime frame
- Difference in smellprints of exhaled breath provided by the eNose before and after chemotherapy.

Secondary

MeasureTime frame
-ad a: difference in smellprints of exhaled breath provided by the eNose between distinct subgroups of lung cancer (adenocarcinoma vs sqamous cell carcinoma vs SCLC) -ad b: relationship between smellprints and stage of lung cancer or SUV on 18FDG-PET (see objectives). -ad c: relationship between smellprints and tumour response classified according to the RECIST [3] criteria

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)