EUCTR2010-022897-14-DK
Active, Not Recruiting
Phase 1
A feasibility study of Multimodal Exercise/Nutrition/Anti-inflammatory treatment for Cachexia - the pre-MENAC study. - A feasibility study of Multimodal Exercise/Nutrition/Anti-inflammatory treatment for Cachexia - the
St. Olavs University Hospital0 sites12 target enrollmentMay 8, 2013
Conditionslung cancerMedDRA version: 16.0Level: LLTClassification code 10025044Term: Lung cancerSystem Organ Class: 100000004864Therapeutic area: Diseases [C] - Cancer [C04]
Drugscelecoxib
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- lung cancer
- Sponsor
- St. Olavs University Hospital
- Enrollment
- 12
- Status
- Active, Not Recruiting
- Last Updated
- 9 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Lung cancer
- •Have a staging CT within 4 weeks of commencement of chemotherapy or chemoradiotherapy (in patients where staging CT is outwith this period, further CT scanning will be undertaken. PET\-CTs are also appropriate)
- •18–75years of age
- •about to start chemotherapy
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1\.2 Adults (18\-64 years) yes
- •F.1\.2\.1 Number of subjects for this age range 10
- •F.1\.3 Elderly (\>\=65 years) yes
- •F.1\.3\.1 Number of subjects for this age range 2
Exclusion Criteria
- •Renal impairment (serum albumin \< 25 g/L or Child\-Pugh \=10 (pancreatic cancer patients only)), creatinine clearance \<30ml/min (estimated using cockroft\-gault, creatinine measured within two months of date of consent)
- •Patients who are taking either aspirin, NSAID or Cox 2 inhibitors prior to study entry
- •Women during pregnancy, breastfeeding or who are of child\-bearing potential (that is not postmenopausal or permanently sterilised) age and who do not use adequate contraception (oral, injected or implanted or hormonal methods of contraception’s, intrauterine device and barrier method)
Outcomes
Primary Outcomes
Not specified
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