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Strength Training on Pancreatic Cancer

Strength Training on Pancreatic Cancer

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01395563
Acronym
STOPC
Enrollment
0
Registered
2011-07-15
Start date
2009-01-31
Completion date
2011-12-31
Last updated
2015-03-13

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

Conditions

Cachexia, Myopathy, Pancreatic Neoplasms

Brief summary

The purpose of this study is to determine whether prednisone, methotrexate, and cyclophosphamide are effective in the treatment of rapidly progressive hearing loss in both ears due to autoimmune inner ear disease (AIED).

Detailed description

Sudden out-of-hospital cardiac arrest (OOH-CA) remains a significant cause of death, in spite of recent declines in overall mortality from cardiovascular disease. Existing methods of emergency resuscitation are inadequate due to time delays inherent in the transport of a trained responder with defibrillation capabilities to the side of the OOH-CA victim. Existing Emergency Medical Services (EMS) systems typically combine paramedic Emergency Medical Technician (EMT) services with some level of community involvement, such as bystander cardiopulmonary resuscitation (CPR) training. Some communities include automated external defibrillators (AEDs) at isolated sites or in mobile police or fire vehicles. A comprehensive, integrated community approach to treatment with AEDs would have community units served by these volunteer non-medical responders who can quickly identify and treat a patient with OOH-CA. Such an approach is termed Public Access Defibrillation (PAD).

Interventions

BEHAVIORALstrength training

strength training, high intensity, twice up to 3 times per week

Sponsors

Heidelberg University
CollaboratorOTHER
Technical University of Munich
CollaboratorOTHER
German Cancer Research Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* patients with pancreatic carcinomas after surgery (resection or exploration) * given consent

Exclusion criteria

* acute infection * pain * no mobility or ability for walking or standing * severe neurological disorders (apoplex, morbus Parkinson, paresis of the lower extremeties) * severe cardiac or cardiovascular diseases (z.B. heart insufficiency NYHA III, myocardial infarction \<3 months) * rhytmical disorders, that contraindicate ergospirometric examinations * cardiac therapy with digitalis pharmacy * unclear syncopes * severe pulmonal insufficiency * renal insufficiency (GFR \< 30% at Krea \>3 mg/dl) * synchronous participation in an other clinical trial

Design outcomes

Primary

MeasureTime frame
muscle mass and strengthafter 8 weeks of intervention

Secondary

MeasureTime frame
quality of lifeafter 8 weeks of intervention

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026