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11941. Feasibility and Cost Analysis of PBSC Mobilization Using Pegfilgrastim in Hematologic Malignancies

: August 31, 2012 Last Update Posted : April 20, 2018 Sponsor: Dartmouth-Hitchcock Medical Center Information provided by (Responsible Party): John M. Hill, Jr., MD, Dartmouth-Hitchcock Medical Center Study Details Study Description Go to Brief Summary: The purpose of this study is to determine the efficacy of Pegfilgrastim in the mobilization of autologous peripheral blood stem cells (PBSCs), defined as cell yield ≥ 3 x 10e6 CD34+/kg and to assess the costs related to Pegfilgrastim use (...) in the mobilization of autologous PBSCs. Also to determine the side effects of Pegfilgrastim in the mobilization of autologous peripheral blood stem cells. Condition or disease Intervention/treatment Phase Hematologic Malignancies Drug: Pegfilgrastim Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 7 participants Intervention Model: Single Group Assignment Masking: None (Open Label) Primary Purpose: Treatment Official Title

2008 Clinical Trials

11942. Impact of Peer Health Workers and Mobile Phones on HIV Care

Health Workers Intervention Behavioral: Peer Health Workers and Mobile Phone Intervention Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 1200 participants Allocation: Randomized Intervention Model: Factorial Assignment Masking: None (Open Label) Primary Purpose: Health Services Research Official Title: Impact of Peer Health Workers and Mobile Phones on HIV Care Study Start Date : March 2006 Actual Primary (...) indexed to this study by ClinicalTrials.gov Identifier (NCT Number): Layout table for additonal information Responsible Party: Larry William Chang, Assistant Professor of Medicine, Johns Hopkins University ClinicalTrials.gov Identifier: Other Study ID Numbers: IRB00000748 First Posted: May 9, 2008 Last Update Posted: March 29, 2012 Last Verified: March 2012 Keywords provided by Larry William Chang, Johns Hopkins University: HIV AIDS Community Health Workers Mobile Phones Adherence Antiretroviral

2008 Clinical Trials

11943. Mobile Phone Based Structured Intervention

in the mobile phone group will monitor their asthma daily using their mobile phone to record symptoms, medication and lung function. Instantaneous feedback to their phone will provide a visual indication of asthma control and prompts about therapy. The patient and their clinician will have web-based access to all readings. People in the control group will use traditional paper-based monitoring. Under the care of their asthma nurse, both groups will be treated according to the step-wise approach of the BTS (...) could provide timely evidence for the use of information technology to address the long-recognised problem of poor asthma control. Condition or disease Intervention/treatment Phase Asthma Behavioral: Mobile phone technology Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Estimated Enrollment : 312 participants Intervention Model: Parallel Assignment Masking: Single (Investigator) Primary Purpose: Supportive Care Official Title

2007 Clinical Trials

11944. Clinical Investigation of the LCS® Complete Posterior Stabilized Mobile-bearing Total Knee System

Not Applicable Detailed Description: Prospective, multi-center study to evaluate the clinical outcome of posterior stabilized design of LCS® Complete Mobile-Bearing Total Knee System. No comparison group. 12 month enrollment, 12 month post-operative evaluation. Follow-up intervals: Pre-op, 3 month, 6 month, and 12 month. Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 210 participants Allocation: Non-Randomized Intervention Model: Single (...) Group Assignment Masking: None (Open Label) Primary Purpose: Treatment Official Title: LCS® PS: A Prospective, Multi-center Clinical Investigation of the LCS® Complete Posterior Stabilized Mobile-bearing Total Knee System Study Start Date : September 2006 Actual Primary Completion Date : February 2011 Actual Study Completion Date : February 2011 Resource links provided by the National Library of Medicine related topics: related topics: Arms and Interventions Go to Arm Intervention/treatment LCS

2007 Clinical Trials

11945. Management of Patients With Type 2 Diabetes and Hypertension Using Mobile Health Care System

Information provided by: Korea University Study Details Study Description Go to Brief Summary: The purpose of this study is to determine whether cellular phone based health care system is effective in the treatment of diabetes and hypertension. Condition or disease Intervention/treatment Phase Diabetes Hypertension Obesity Device: Mobile Health Care System (DrUB) Not Applicable Detailed Description: Diabetes care is facilitated by a patient's being engaged in a self-management program with the advice (...) information Principal Investigator: Kyung M Choi, MD Department of Internal Medicine, Korea University College of Medicine More Information Go to Publications: Layout table for additonal information Responsible Party: Kyung Mook Choi, Korea University ClinicalTrials.gov Identifier: Other Study ID Numbers: Seoul R&BD Program First Posted: June 21, 2007 Last Update Posted: May 20, 2008 Last Verified: May 2008 Keywords provided by Korea University: Mobile Health Units Chronic Disease Additional relevant MeSH

2007 Clinical Trials

11946. EMEPIC : Value of a Mobile Team of Cardiologist Using Echocardiography for Managing Patients With Acute Heart Failure

is that a mobile team will lead to shorter hospitalization. Condition or disease Intervention/treatment Phase Acute Heart Failure Congestive Edema Cardiac Disease Procedure: Mobile team Procedure: Standard care Not Applicable Detailed Description: Randomized, controlled, monocentric study comparing Standard care with the care provided by a mobile team including a cardiologist with mobile echocardiography, systematic follow up à 3 days, a dietician advice in patients hospitalized for acute heart failure (...) Using Echocardiography for Managing Patients With Acute Heart Failure Study Start Date : February 2008 Actual Primary Completion Date : June 2010 Actual Study Completion Date : July 2010 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: 1 Mobile Team Procedure: Mobile team a mobile team including a cardiologist with mobile echocardiography, systematic follow up à 3 days, a dietician advice in patients

2007 Clinical Trials

11947. AMD3100 (Plerixafor) in Multiple Myeloma (MM) or Non-Hodgkin's Lymphoma (NHL) Patients Predicted to be Unable to Mobilize With G-CSF Alone

are currently enrolled in another experimental protocol during the mobilization phase Had an apheresis yield >1.3*10^6 CD34+ cells/kg on Day 5 (Applicable only to patients who, after 5 days of G-CSF mobilization, have peripheral blood (PB) CD34+ count of 8-19 cells/µl inclusive). Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please (...) Assignment Masking: None (Open Label) Primary Purpose: Treatment Official Title: Effect of AMD3100 (240µg/kg) on the Apheresis Yield of CD34+ Cells When Given To Multiple Myeloma or Non-Hodgkin's Lymphoma Patients Predicted to be Unable to Mobilize ≥2 x 10^6 CD34+ Cells in Three Apheresis Days When Given G-CSF Alone Study Start Date : April 2005 Actual Primary Completion Date : July 2005 Actual Study Completion Date : August 2006 Resource links provided by the National Library of Medicine related topics

2006 Clinical Trials

11948. C2P Mobilization Intervention (Pilot)

and Alcoholism (NIAAA) Information provided by (Responsible Party): University of North Carolina, Chapel Hill Study Details Study Description Go to Brief Summary: Connect to Protect (C2P): Partnerships for Youth Prevention Interventions is a multi-site, three-phase project developed by the Adolescent Medicine Trials Network for HIV/AIDS Interventions (ATN). The overall goal of the project is to ultimately reduce HIV incidence and prevalence in youth 12-24 years old through a community mobilization (...) intervention. This protocol (ATN 040) describes part one of Phase III. Part two of Phase III will be submitted as a separate protocol (ATN 041). Condition or disease Intervention/treatment Phase HIV Infections Behavioral: Community Mobilization Not Applicable Detailed Description: The objective of Phase III is to initiate and complete a community mobilization intervention aimed at ultimately reducing HIV incidence and prevalence among youth. The intervention will consist of guiding C2P coalitions through

2005 Clinical Trials

11949. Virtual Reality Mobility Training System for Veterans With Vision Loss

Information provided by (Responsible Party): VA Office of Research and Development ( US Department of Veterans Affairs ) Study Details Study Description Go to Brief Summary: This is a two-year proof-of-concept study to evaluate a new Virtual Reality (VR) "holographic" sound system for use as an audiological Orientation and Mobility (O&M) training tool Condition or disease Intervention/treatment Phase Blindness Device: Virtual Sound System Not Applicable Detailed Description: This is a two-year proof (...) Criteria: Imbalance between ears - HL difference of 20 db HL or more Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00333879 Locations Layout table for location information United States, Georgia Atlanta VA Medical and Rehab Center, Decatur Decatur

2006 Clinical Trials

11950. Effects of Dynamic Wheelchair Seating on Spasticity and Functional Mobility in Children

Intervention/treatment Phase Cerebral Palsy, Spastic Device: Dynamic Wheelchair Seating System Not Applicable Detailed Description: Specifically, it is expected that range of motion and functional mobility in the hip, knee, and ankle joints will increase, involuntary spasticity in the musculature of the mid and lower body will be reduced, and independent daily function will be enhanced in children with CP. The success of these conditions will greatly influence the child's interaction with the surrounding (...) : None (Open Label) Primary Purpose: Treatment Official Title: Effects of Dynamic Wheelchair Seating on Spasticity and Functional Mobility in Children Study Start Date : April 2006 Actual Primary Completion Date : August 2007 Actual Study Completion Date : August 2007 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Outcome Measures Go to Primary Outcome Measures : Joint range of motion Muscle spasticity Functional Capacity Assessments

2006 Clinical Trials

11951. Comparison Between Fixed- Versus Mobile-bearing TKA

of the study is to analyse the clinical and radiological results of a postero-stabilized TKA by using a mobile bearing versus fixed. Only patients with medial femorotibial arthritis will be included. The consequences on the patellofemoral joint will be thoroughly analysed on skyline view. Condition or disease Intervention/treatment Phase Knee Arthritis Device: mobile-bearing TKA Device: fixed- bearing TKA Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (...) Comparison Between Fixed- Versus Mobile-bearing TKA Comparison Between Fixed- Versus Mobile-bearing TKA - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Comparison Between Fixed- Versus Mobile-bearing TKA

2007 Clinical Trials

11952. Post-operative Mobilization for Carpal Tunnel Syndrome

Purpose: Treatment Official Title: Post-operative Mobilization for Carpal Tunnel Study Start Date : December 2006 Actual Primary Completion Date : February 2011 Actual Study Completion Date : February 2011 Resource links provided by the National Library of Medicine related topics: related topics: resources: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: 1 Procedure: Carpal tunnel release surgery Patient will have carpal tunnel release surgery and will be put in a splint (...) Post-operative Mobilization for Carpal Tunnel Syndrome Post-operative Mobilization for Carpal Tunnel Syndrome - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Post-operative Mobilization for Carpal Tunnel

2007 Clinical Trials

11953. Effect of Mobile Communication With a Cellular Phone With a Glucometer on Glucose Control in Type 2 Diabetic Patients

Effect of Mobile Communication With a Cellular Phone With a Glucometer on Glucose Control in Type 2 Diabetic Patients Effect of Mobile Communication With a Cellular Phone With a Glucometer on Glucose Control in Type 2 Diabetic Patients - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number (...) of saved studies (100). Please remove one or more studies before adding more. Effect of Mobile Communication With a Cellular Phone With a Glucometer on Glucose Control in Type 2 Diabetic Patients The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT00412178 Recruitment Status : Terminated First Posted

2006 Clinical Trials

11954. Evaluation of Traditional Paper Symptom Diary vs. the VOCEL Mobile Diary

& Asthma Medical Group & Research Center Study Details Study Description Go to Brief Summary: This study is designed to evaluate a traditional paper symptom diary system versus the VOCEL Mobile Diary. Subjects will be issued in a random order each system and asked their preference at the end of their participation. Condition or disease Intervention/treatment Phase Asthma Drug: Alvesco (Ciclesonide) 160 ug/day Not Applicable Detailed Description: Inflammation is the underlying pathophysiologic process (...) of Traditional Paper Symptom Diary vs. the VOCEL Mobile Diary The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT00367263 Recruitment Status : Completed First Posted : August 22, 2006 Last Update Posted : May 2, 2007 Sponsor: Allergy & Asthma Medical Group & Research Center Information provided by: Allergy

2006 Clinical Trials

11955. Exercise in Improving Mobility and Reducing Fatigue and/or Weakness in Older Cancer Survivors

is studying exercise to see how well it works compared to standard therapy in improving mobility and reducing fatigue and/or weakness in older cancer survivors. Condition or disease Intervention/treatment Phase Bladder Cancer Breast Cancer Colorectal Cancer Esophageal Cancer Fatigue Lung Cancer Lymphoma Ovarian Cancer Prostate Cancer Behavioral: exercise intervention Procedure: complementary or alternative medicine procedure Procedure: fatigue assessment and management Procedure: physical therapy (...) Not Applicable Detailed Description: OBJECTIVES: Compare the perception of, and the patterns of change in fatigue, weakness, physical activity level, and functional status in elderly cancer survivors who undergo Resistance Exercise via Negative-Eccentric Work (RENEW) vs standard care. Compare changes in muscle structure, function (strength + power production and metabolic function) and mobility. Evaluate the patient's adherence to and satisfaction with the RENEW intervention. OUTLINE: This is a prospective

2006 Clinical Trials

11956. Evaluating the Safety of G-CSF Mobilization in Individuals With Beta Thalassemia Major

of the participants will receive hydroxyurea (HU) prior to G-CSF mobilization. HU is used in splenectomized patients to attempt to reduce the risk of clotting during mobilization. In non-splenectomized patients, HU is given in an attempt to decrease the size of the spleen. Condition or disease Intervention/treatment Phase Beta-Thalassemia Drug: Hydroxyurea Not Applicable Detailed Description: Primary Objective: To determine the safety of PBSC mobilization with G-CSF, with or without HU pretreatment in adults (...) : None (Open Label) Primary Purpose: Treatment Official Title: A Pilot Study to Assess the Safety and Efficacy of G-CSF Mobilization With and Without Hydroxyurea Pretreatment in Adults With Beta Thalassemia Major Study Start Date : July 2006 Actual Primary Completion Date : August 2010 Actual Study Completion Date : August 2010 Resource links provided by the National Library of Medicine related topics: related topics: available for: resources: Arms and Interventions Go to Arm Intervention/treatment

2006 Clinical Trials

11957. Randomized Fixed Bearing vs Mobile Bearing Cruciate Substituting TKA

Randomized Fixed Bearing vs Mobile Bearing Cruciate Substituting TKA Randomized Fixed Bearing vs Mobile Bearing Cruciate Substituting TKA - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Randomized Fixed (...) Bearing vs Mobile Bearing Cruciate Substituting TKA The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT00289107 Recruitment Status : Completed First Posted : February 9, 2006 Results First Posted : December 10, 2010 Last Update Posted : August 14, 2013 Sponsor: DePuy Orthopaedics Information provided

2006 Clinical Trials

11958. Randomized Fixed Bearing vs Mobile Bearing Cruciate Retaining TKA

Randomized Fixed Bearing vs Mobile Bearing Cruciate Retaining TKA Randomized Fixed Bearing vs Mobile Bearing Cruciate Retaining TKA - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Randomized Fixed Bearing (...) vs Mobile Bearing Cruciate Retaining TKA The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT00289094 Recruitment Status : Completed First Posted : February 9, 2006 Results First Posted : December 10, 2010 Last Update Posted : August 14, 2013 Sponsor: DePuy Orthopaedics Information provided

2006 Clinical Trials

11959. Impact of Pushrim Activated Power Assist Wheelchairs on Mobility Among People With Tetraplegia

Impact of Pushrim Activated Power Assist Wheelchairs on Mobility Among People With Tetraplegia Impact of Pushrim Activated Power Assist Wheelchairs on Mobility Among People With Tetraplegia - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one (...) or more studies before adding more. Impact of Pushrim Activated Power Assist Wheelchairs on Mobility Among People With Tetraplegia The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT00281463 Recruitment Status : Completed First Posted : January 24, 2006 Results First Posted : November 18, 2014 Last Update

2006 Clinical Trials

11960. Study on the Efficacy and Mechanism of Cardiac Rehabilitation for Stem Cell Mobilization and Heart Failure Improvement

Study on the Efficacy and Mechanism of Cardiac Rehabilitation for Stem Cell Mobilization and Heart Failure Improvement Study on the Efficacy and Mechanism of Cardiac Rehabilitation for Stem Cell Mobilization and Heart Failure Improvement - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum (...) number of saved studies (100). Please remove one or more studies before adding more. Study on the Efficacy and Mechanism of Cardiac Rehabilitation for Stem Cell Mobilization and Heart Failure Improvement The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT00154466 Recruitment Status : Completed First

2005 Clinical Trials

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