Cancer Control
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Current Cancer Control Protocols

   Updated 05/13/2008           

(New Protocols in Red)

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Contact Information

Montana Cancer Consortium 90 Poly Dr  Suite 2      Billings, MT  59101      Phone 406-259-2245      800-528-3340                 Fax  259-2682                Email mccinfo@mtcancer.org


 


 

       List by Protocol Number

 Informational

NCCTG N0392   Consent    HIPAA    Protocol

Assessment of Patient Satisfaction with Participation in Phase II/III NCCTG Clinical Trials

NSABP LTS-01    Consent    HIPAA    Protocol 

Patient Reported Outcomes in Long-term Survivors with Colon and Rectal Cancer

 Symptom Management

Ascites

NCCTG N04C2    Consent   HIPAA    Protocol  

An Exploratory, Randomized, Placebo-Controlled Trial of Depot Octreotide for Symptomatic Ascites in Cancer Patients

Neuropathy

NCCTG N06CA     Consent    HIPAA     Protocol  (permanent closure effective 05/16/08)

The Use of Topical Baclofen, Amitriptyline HCl, and Ketamine (BAK) in a PLO Gel vs. Placebo for the Treatment of Chemotherapy Induced Peripheral Neuropathy:  A Phase III Randomized Double-Blind Placebo Controlled Study

Fatigue

NCCTG N05C7   Consent   HIPAA   Protocol   

Long  Acting Methylphenidate (Concerta™) for Cancer-Related Fatigue:  A Phase III Randomized, Double-Blind Placebo Controlled Study

Ovarian Function Failure

SWOG S0230    Consent     HIPAA  Fast Facts   Protocol

Phase III Trial of LHRH Analog Administration During Chemotherapy to Reduce Ovarian Failure Following Standard Adjuvant Chemotherapy in Early Stage, Hormone-Receptor Negative Breast Cancer

Vaginal Dryness

NCCTG N04CA   Consent     HIPAA   Protocol                    

Pilocarpine for Vaginal Dryness:  A Phase III Randomized, Placebo-controlled, Double-blind Study

Hand and Foot Syndrome

NCCTG N05C5   Consent B   HIPAA      Protocol

A Phase III Randomized, Placebo-controlled, Double-blind Trial to Determine the Effectiveness of a Urea/Lactic Acid-based Topical Keratolytic Agent and Vitamin B-6 for Prevention of Capecitabine-induced Hand and Foot Syndrome

Radiation Oncology

RTOG R0518     Consent    HIPAA     Protocol   Supplemental Funding

Phase III, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy of Zometa for the Prevention of Osteoporosis and Associated Fractures in Patients Receiving Radiation Therapy and Long-term LHRH Agonists for High-Grade and/or Locally Advanced Prostate Cancer 

RTOG R0517     Consent    HIPAA   Protocol

Randomized Phase III trial to Evaluate Radiopharmaceuticals and Zoledronic Acid in the Palliation of Osteoblastic Metastases from Lung, Breast and Prostate Cancer

 

 

 

        Prevention

SWOG E5597    Consent   Patient Letter    HIPAA    Protocol

Phase III   Chemoprevention Trial of Selenium Supplementation in Persons with Resected Stage I Non-Small Cell Lung Cancer

SWOG S0437      Consent     HIPAA

PCPT Extension Study

SWOG S0000  Consent       Consent -Anc

SELECT - Prostate Cancer Prevention -closed to accrual

SWOG S0000A PREADVISE   Consent-initial   HIPAA  Consent-secondary    (Open only to SELECT participants)

SWOG S0000B  SEE   Consent    HIPAA (Open only to SELECT Participants)

 
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