Skip to content

Feasibility study of adjuvant chemotherapy with cisplatin and pemetrexed short hydration regimen for completely resected NSCLC

Feasibility study of adjuvant chemotherapy with cisplatin and pemetrexed short hydration regimen for completely resected NSCLC - Feasibility study of adjuvant chemotherapy with cisplatin and pemetrexed short hydration regimen for completely resected NSCLC

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000010336
Enrollment
21
Registered
2013-04-01
Start date
2013-04-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Completely resected NSCLC(non-squamous cell carcinoma, stage II - IIIA)

Interventions

Dose:day1 CDDP 75mg/m2+PEM 500 mg/m2 with short hydration Cycle: 4 cycles

Sponsors

Division of Respiratory Medicine, Department of Internal Medicine,Kobe University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)The patient histologically proven as non-small cell lung cancer (2)The patient with p-staged II - IIIA that received segmentectomy, lobectomy, or bi-lobectomy (3) Performance Status is 0 - 1 (ECOG). (4) 20 years of age or older, 75 years of age or younger. (5) The patient who does not receive any chemotherapy, radiotherapy, or immunotherapy prior to resection (6) The patient who preserves the main organ ( the bone marrow, liver, kidney and so on ) (7) The patient who can receive chemotherapy within 4 - 8 weeks after resection (8) The patient who gives written informed consent

Exclusion criteria

Exclusion criteria: (1)The patient with infection (2)The patient with fever (equal to or more than 38 C) (3)The patient with heavy complication (4)The patient with active double-cancer (5)The patient with uncontrolled pleural effuson (6)The patient with a motor-palsy or figure of peripheral-nerve-disease (7)The patient with drug hypersensitivity (8)The patient with common use of NSAIDs (9)The expectant mother, the woman who has a lactating-woman and the possibility of the pregnancy (10)The patient judged as unsuitable by the doctor

Design outcomes

Primary

MeasureTime frame
Chemotherapy compliance in the four cycles

Secondary

MeasureTime frame
1.safety 2.extraction rate from hospitalization to outpatient clinic 3.2-years disease free survival

Countries

Japan

Contacts

Public ContactMotoko Tachihara

Kobe University Graduate School of Medicine Division of Respiratory Medicine, Department of Internal Medicine,

mt0318@med.kobe-u.ac.jp078-382-5846

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026