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11981. Effects of Sun Filters on Age-related Macular Degeneration in People With Lens Implants

surgery in both eyes with implanted lenses may be eligible for this study. Participants undergo the following procedures: Wear the filter glasses when outdoors between 10:00 a.m. and 4:00 p.m. Record the time of day and light environment when they use the glasses. Have an eye examination, pictures of the retina, and a medical history taken at the beginning of the study and at set intervals during the study. The study lasts at least 12 months and may be extended for a longer period of time Condition (...) participants Time Perspective: Prospective Official Title: Noninvasive Optical Imaging of the Effects of External Spectral Filters on Macular Autofluorescence in Pseudophakic Eyes Study Start Date : June 14, 2007 Study Completion Date : May 4, 2012 Resource links provided by the National Library of Medicine related topics: related topics: Groups and Cohorts Go to Outcome Measures Go to Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study

2007 Clinical Trials

11982. Evaluating the Collaborative Management in Pediatrics (CMP) Training Program Among Pediatric Resident Doctors and Their Patients With Asthma or Obesity

the patient's health. Examples of self-care behaviors include reading books or other materials about relevant health care topics, exercising, following a low-fat diet, seeing a doctor on a regular basis, and making lifestyle changes. It is crucial that doctors, case managers, nurses, pharmacists, and other medical professionals understand the challenges that patients face when attempting to incorporate these self-care behaviors into their lives. Currently, there are few collaborative management programs (...) : Collaborative Management in Pediatrics (CMP) Program Not Applicable Detailed Description: Collaborative management health care involves strengthening and supporting self-care among people with long-term illnesses while assuring that effective medical, preventive, and health maintenance treatments occur. In collaborative management, it is important for patients, family members, and health care providers to understand each other's roles and responsibilities as they work toward a shared goal of improving

2007 Clinical Trials

11983. Treatment of Acute Promyelocytic Leukemia With All-Trans Retinoic Acid (ATRA) and Idarubicin (AIDA)

+ Methotrexate + Mercaptopurine Salvage Therapy for Molecular and Haematological Relapses Study Start Date : March 1999 Actual Primary Completion Date : August 2007 Actual Study Completion Date : November 2007 Resource links provided by the National Library of Medicine related topics: related topics: available for: resources: Arms and Interventions Go to Outcome Measures Go to Primary Outcome Measures : To evaluate the efficacy of AIDA with a dose reduction in patients older than 70 years of age (...) of molecular remission (PML/RARa negative by RT-PCR) in the successive therapeutic phases with special emphasis on patients with a higher risk for relapse [ Time Frame: 2 years ] Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using

2007 Clinical Trials

11984. A Phase IV Study to Evaluate the Immunogenicity and Safety in UK Laboratory Workers of Menitorix

may contact the study research staff using the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 18 Years and older (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: Yes Criteria Inclusion Criteria: No contraindications to vaccination as specified in the "Green Book" - Immunisation Against Infectious Disease, HMSO. Written informed consent Exclusion Criteria: Known or suspected pregnancy Contacts (...) Assignment Masking: None (Open Label) Primary Purpose: Prevention Official Title: A Phase IV, Single Group Study to Evaluate the Immunogenicity and Safety in UK Laboratory Workers of a Licensed Hib and Meningococcal C Conjugate Combined Vaccine (Menitorix) Study Start Date : July 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 : Determine serum

2007 Clinical Trials

11985. Effectiveness of Protected Environment Rooms for AML and MDS

and older to receive initial treatment in the PE at M. D. Anderson. The PE is a series of rooms containing a special air-flow system that is designed to filter out germs that can cause serious infection. Patients stay in a PE room, without leaving, for up to 5 weeks. In an attempt to keep a PE room germ-free, only the medical staff is allowed in the room. Family and visitors can see the patient, but are separated from the patient by a glass wall. Each PE room has a laptop computer that can be connected (...) to the internet. Books, newspapers, and various other materials are only allowed in the PE room after they have been sterilized for safety reasons. Therapy given to patients with AML or MDS has recently changed from higher (which usually meant that there was more possibility for infections and a need for hospitalization) to lower intensity. Because the value of the PE was already established in patients receiving higher-intensity therapy, researchers want to learn about the value of the PE in patients

2007 Clinical Trials

11986. Response of Older Adults to Influenza Vaccination With Regard to Cytomegalovirus (CMV) Status

this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 50 Years to 80 Years (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: Yes Criteria Inclusion Criteria: No contraindications to vaccination as specified in the "Green Book" - Immunisation Against Infectious Disease, HMSO. Written informed consent obtained Subject aged no less than 50 (...) : Public Health England Collaborator: Royal Free and University College Medical School Information provided by: Public Health England Study Details Study Description Go to Brief Summary: The study is being undertaken to evaluate responses to seasonal influenza vaccine in older adults with respect to their CMV status. CMV is cytomegalovirus and is an organism that infects many people, but does not usually cause disease in the individual unless they are immunocompromised i.e. their immune system

2007 Clinical Trials

11987. Evaluation of a Health at Every Size vs a Behavioral Weight Loss Approach for Obese Women

bariatric surgery Plans to have bariatric surgery over next 2.5 years 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): NCT00769717 Locations Layout table for location information United States, Pennsylvania The Reading Hospital and Medical Center West (...) studies before adding more. Evaluation of a Health at Every Size vs a Behavioral Weight Loss Approach for Obese Women 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: NCT00769717 Recruitment Status : Unknown Verified August 2009 by The Reading Hospital and Medical Center. Recruitment status was: Active

2008 Clinical Trials

11988. Team Based Initiative Support

to 88. Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 18 Years and older (Adult, Older Adult) Sexes (...) Eligible for Study: All Accepts Healthy Volunteers: No Criteria Inclusion Criteria: The primary family member caregiver of the Traumatic Brain Injury (TBI) veteran Veteran receiving care at the Memphis Veterans Affairs Medical Center Perceived need of help and support Willing to participate in the study after discussion with OEF/OIF Program Manager or team member Exclusion Criteria: - None Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you

2008 Clinical Trials

11989. Contingency Management of Psychostimulant Abuse in the Severely Mentally Ill

Phase: 3 months (1 measuresment a month) ] Symptoms of mental illness [ Time Frame: Monthly throughout the study ] Community outcomes (jail bookings, ER visits, mental health outcomes) [ Time Frame: The entire study period and three months prior and after study involvement ] Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join (...) ) to participate in the study. Exclusion Criteria: Any medical/psychiatric condition, or severity of that condition, that, in the opinion of Dr. Ries, the PI, would compromise safe study participation Chart defined organic brain disorder or dementia; Current participation in a methadone maintenance program; Any other circumstances that in the PI's opinion precludes safe study participation. Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you

2008 Clinical Trials

11990. Active Management for Low Back Pain for 6 to 8 Year Old Schoolchildren

the students will get a Back Comic-Book (promotes active management) after the first assessment. The control group will have no other intervention than the questionnaire. Condition or disease Intervention/treatment Phase Low Back Pain Behavioral: Education (Back Comic-Book) Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Estimated Enrollment : 700 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: Double (...) (Participant, Outcomes Assessor) Primary Purpose: Prevention Official Title: Active Management for Low Back Pain Taught to 6 to 8 Year Old Schoolchildren Study Start Date : February 2009 Actual Primary Completion Date : May 2009 Actual Study Completion Date : June 2009 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: 1 The intervention group will receive prevention of low back pain education through a Back

2008 Clinical Trials

11991. A Web-Based Stem Cell Transplant Support System or Standard Care in Young Patients Undergoing Stem Cell Transplant and Their Families

to collecting data for later analysis, the Web site tracking system allows for further tailoring of information and support for the user, principally by time post transplant. Arm II: Each dyad receives institution-specific usual care for 6 months as described in arm I. Accompanying parents also receive a book from the Blood and Marrow Transplant Information Network (BMT InfoNet). Each dyad completes quality-of-life assessment (Child Health Ratings Inventory [CHRIs]-General and CHRIs-HSCT) at day 45 (...) Recruitment Status : Completed First Posted : October 31, 2008 Last Update Posted : July 13, 2011 Sponsor: Tufts Medical Center Collaborator: National Cancer Institute (NCI) Information provided by: Tufts Medical Center Study Details Study Description Go to Brief Summary: RATIONALE: A Web site for stem cell transplant health information and support may be effective in helping parents improve their health-related knowledge, skills, and quality of life, which may also improve their children's quality

2008 Clinical Trials

11992. An Educational and Exercise Program as Secondary Prevention of Recurrent Lower Back Pain in Healthcare Workers

, the economic consequences are enormous (accounting for 70 to 80% of the total cost of lower back pain). Nowadays, some very general training sessions are offered to workers at Lyon University Medical Center, irrespective of their lower back pain status. These very general training sessions are mostly preventive and primary in nature (like back school program) despite the fact that these people already have a history of lower back pain, the main risk factor of recurrence and chronic pain. Since the 1980 (...) , 2008 Last Update Posted : December 2, 2014 Sponsor: Hospices Civils de Lyon Information provided by (Responsible Party): Hospices Civils de Lyon Study Details Study Description Go to Brief Summary: At Lyon University Medical Center, back problems are the leading cause of sick leave. The course of lower back pain is usually relatively short (recovery occurs within 4 to 6 weeks in 90% of cases). However, about 5-10% develop chronic lower back pain. Although this is a relatively small group

2008 Clinical Trials

11993. Testing the Effectiveness of Child and Parent-Targeted Health Promotion Interventions in Pediatric Stem Cell Transplantation

to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 6 Years to 18 Years (Child, Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers (...) of parental positive affect and distress. Additional objectives of the study include examining the impact of the intervention on short-term medical outcomes, as well as measures of child health-related quality of life and parent and child post-traumatic stress symptoms (PTSS) at 6 months post-BMT. Analyses will explore hypotheses specific to the positive psychology model, testing the role of positive affect and dispositional optimism as mediators and moderators of the intervention on child and parent well

2008 Clinical Trials

11994. Evaluation Cardiac Function With Echo and BNP in Obstetrical Patients With/Without Cardiac Disease

Information Services, New York 1990; 1465-1478. Clark SL. Structural cardiac disease in pregnancy. Clark SL, Cotton DB, Phelan JP (eds). Critical Care Obstetrics, Medical Economics Books, Oradell, New Jersey 1987; 92-113. Layout table for additonal information Responsible Party: John J. Folk, M.D. Associate Professor, SUNY Upstate Medical University Department Obstetrics & Gynecology ClinicalTrials.gov Identifier: Other Study ID Numbers: IRBPHS 5123 First Posted: September 25, 2008 Last Update Posted (...) one or more studies before adding more. Evaluation Cardiac Function With Echo and BNP in Obstetrical Patients With/Without Cardiac Disease 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: NCT00759733 Recruitment Status : Unknown Verified August 2010 by State University of New York - Upstate Medical

2008 Clinical Trials

11995. Renoprotective Effects of Fluid Prophylaxis Strategies for Contrast Induced Nephropathy (CIN)

, you or your doctor may contact the study research staff using the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 20 Years and older (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: No Criteria Inclusion Criteria: Booked for cardiac angiography and/or percutaneous coronary intervention Pre-existing reduced kidney function (estimated GFR < 60 mls/min/1.73m2 by MDRD equation[18]). Minimum age 20 years (...) Nephropathy Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: 1 Intravenous sodium bicarbonate (130 mEq/L) in 4.35% dextrose at 3.5 ml/Kg over 1 hour pre-contrast, followed by the same solution intravenously at 1 ml/Kg/hr for 6 hours Drug: Bicarbonate Hydration Intravenous sodium bicarbonate (130 mEq/L) in 4.35% dextrose at 3.5 ml/Kg over 1 hour pre-contrast, followed by the same solution

2008 Clinical Trials

11996. Epidural Steroid Injection Versus Epidural Steroid Injection and Manual Physical Therapy and Exercise in the Management of Lumbar Spinal Stenosis

will be treated additionally with a physical therapy program emphasizing lumbar flexion exercises, aerobic and strength/ conditioning exercises, and manual physical therapy as well as receiving up to 3 epidural steroid injection(s) and educational support using The Back Book. Epidural steroid injection Other: Epidural steroid injection Patients in the ESI Group will be treated with up to 3 epidural steroid injections, educational support, and general care by the treating physician. Outcome Measures Go (...) : 10 weeks, 6 months, 12 months ] Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 50 Years to 90 Years

2008 Clinical Trials

11997. Photon/Proton Radiation Therapy for Carcinoma of the Nasopharynx

by (Responsible Party): University of Florida Study Details Study Description Go to Brief Summary: The purpose of this study is to collect outcomes information to see what effects photon/proton beam radiation has on nasopharynx cancer. Condition or disease Nasopharynx Cancer Detailed Description: Data collection will be obtained from the patient's medical records including initial evaluation, pathology report, dosimetry information, radiotherapy completion records and follow-up. Study Design Go to Layout (...) table for study information Study Type : Observational Actual Enrollment : 9 participants Observational Model: Cohort Time Perspective: Prospective Official Title: A Clinical Outcomes Protocol of Photon/Proton Beam Radiation Therapy for Carcinoma of the Nasopharynx Study Start Date : June 2008 Actual Primary Completion Date : July 2015 Actual Study Completion Date : July 2015 Resource links provided by the National Library of Medicine resources: Groups and Cohorts Go to Group/Cohort Photon/Proton

2008 Clinical Trials

11998. Mom: Managing Our Mood, Part of The Family Help Program

Frame: end of intervention ] Beck Depression Inventory-II [ Time Frame: baseline, 120, 240 and 365 day follow-up ] Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Layout (...) by a professional team. MOM is not designed to replace specialist care of complex multi-problem mothers. Eligible participants will be randomly assigned to either active MOM treatment or to the Best Efforts control condition. Those participants assigned to Best Efforts receive printed information about postpartum depression that describes the illness, how it is caused and various treatment options; they are assigned a Coach who books their assessments and is available to answer any questions

2008 Clinical Trials

11999. Management of Nausea and Vomiting of Pregnancy

. Women who have already received treatment for NVP outside of this trial. Pregnant women who present who will not be booking at CUMH for their pregnancy or are not resident in the South West of Ireland i.e. day care treatment is not an option. Women who do not have a good understanding of English. 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 (...) (Clinical Trial) Actual Enrollment : 98 participants Allocation: Randomized Intervention Model: Single Group Assignment Masking: None (Open Label) Primary Purpose: Treatment Official Title: Randomized Controlled Trial of Day Care Versus Inpatient Management of Nausea and Vomiting of Pregnancy Study Start Date : April 2009 Actual Primary Completion Date : September 2012 Actual Study Completion Date : September 2012 Resource links provided by the National Library of Medicine related topics: Arms

2008 Clinical Trials

12000. Autologous or Syngeneic Stem Cell Transplant Followed by Donor Stem Cell Transplant and Bortezomib in Treating Patients With Newly Diagnosed High-Risk, Relapsed, or Refractory Multiple Myeloma

/Nonmyeloablative Allogeneic HCT From HLA-Matched Related and Unrelated Donors Followed by Bortezomib Maintenance Therapy for Patients With High-Risk Multiple Myeloma Study Start Date : October 2008 Actual Primary Completion Date : October 2016 Resource links provided by the National Library of Medicine related topics: related topics: available for: resources: Arms and Interventions Go to Arm Intervention/treatment Experimental: Tandem Auto-/Nonmyeloablative Allo-HCT and Maintenance Therapy See Detailed (...) Transplantation [ Time Frame: Up to 100 days after the autograft or allograft ] Confidence intervals will be estimated. Non-relapse Mortality [ Time Frame: 200 and 365 days after allo ] Confidence intervals will be estimated. Assessed at 200 days and 1 year after allograft. OS [ Time Frame: At 2 years after the autograft ] Estimated by the method of Kaplan and Meier. Confidence intervals will be estimated. Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate

2008 Clinical Trials

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