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12001. Improving Outcomes in Underserved Women With GDM

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 to 45 Years (Adult) Sexes Eligible for Study: Female Accepts Healthy Volunteers: No Criteria Inclusion (...) Phase Diabetes Mellitus Pregnancy Other: telemonitoring Other: Standard of care Not Applicable Detailed Description: Using a step care design, women will be randomized into standard of care or Telemonitoring. In the standard of care group, women will monitor their blood glucose levels four times a day, perform fetal movement counting three times a day and also record insulin doses. The women will record this information in a logbook, which will be reviewed by the medical team at prenatal visits

2008 Clinical Trials

12002. Magnetic Resonance (MR) Spectroscopy in Localized Prostate Cancer

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: Over 18 years Localized prostate cancer patients Signed informed consent form Exclusion Criteria: Contacts and Locations Go to Information from the National Library of Medicine To learn more about (...) and after filling the rectum with barium. Patients will be requested to take a mild laxative of their choice the night before the exam, and not to eat for 2-4 hours prior to the scan. To facilitate this, that patient's exam will be booked prior to lunch. Prior to the exam, the patient will be asked to empty their bladder and 40 mg of Buscopan will be administered to the patient (i.m. of i.v.) to reduce peristalsis, the presence of which degrades the quality of NMR scans. The patient will lie on a board

2008 Clinical Trials

12003. Non-Invasive Brain Signal Training to Induce Motor Control Recovery After Stroke

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: 22 Years and older (Adult, Older Adult) Sexes Eligible for Study (...) : All Accepts Healthy Volunteers: Yes Criteria Inclusion Criteria: medically stable and >/= 6 months post stroke difficulty using upper limb for functional tasks >21 years old Exclusion Criteria: chronic, progressive medical condition (i.e. Parkinson's disease) 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

2008 Clinical Trials

12004. Intermittent Preventive Treatment (IPTp) Versus Rapid Diagnostic Testing (RDT) and Treatment of Malaria in Pregnancy

to 24 weeks at their first booking. She is willing to participate and complete the test schedule, and has given informed consent. She is willing to have supervised delivered at maternity units in the district. She lives within the study district. Exclusion Criteria: She has a past obstetric and medical history that will adversely affect the interpretation of outcomes such as repeated stillbirths and eclampsia. She has a haemoglobin level below 5.0 g/dl. She has malaria that is severe enough (...) to require parenteral medication. 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): NCT00432367 Locations Layout table for location information Ghana Juaben Government Hospital Juaben, Ashanti, Ghana Sponsors and Collaborators London School of Hygiene

2007 Clinical Trials

12005. Neural Effects of Mindfulness Training on Attention

and withhold from pressing the space bar for the target. 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 (...) who had expertise in nutrition and offered a program described in the book, Nutrition for Life by Lisa Hark. Behavioral: Nutrition Education course 8-week course in nutrition Outcome Measures Go to Primary Outcome Measures : Reaction Times on the Sustained Attention to Response Task. [ Time Frame: 9 weeks ] Single digits (0-9) are flashed on the screen one by one. The number 3 is the target and all other digits are non-targets. The participant is asked to press the space bar for nontargets

2006 Clinical Trials

12006. IPT of Malaria With SP in Different Zones of Drug Resistance in Rwanda

With SP in Different Zones of Drug Resistance in Rwanda 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: NCT00372632 Recruitment Status : Completed First Posted : September 7, 2006 Last Update Posted : September 14, 2010 Sponsor: Institute of Tropical Medicine, Belgium Information provided by: Institute (...) of Tropical Medicine, Belgium Study Details Study Description Go to Brief Summary: The present study will address the question whether the use of IPT using SP in pregnancy is efficacious in Rwanda, where it is going to be used for the first time, in areas with high levels of SP resistance. While the implementation of the new policy will take place in areas at low SP resistance level, where we expect pregnant women and newborns to benefit from it, it is of paramount importance to clarify which is the real

2006 Clinical Trials

12007. Wellness Interventions After Transplant Study

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: Yes Criteria Inclusion Criteria (...) such as suicide attempts or a psychosis medically unstable (a hospital admission for non-elective purposes in the last 3 months or major surgery planned in the next 3 months) on dialysis regularly practicing mindfulness meditation 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

2006 Clinical Trials

12008. Oral Allergy Syndrome (OAS): a Pilot Study to Evaluate a Clinical Questionnaire as a Diagnostic Tool

Aged 16 years or more Exclusion Criteria: Pregnancy Existing medical condition which could be affected by a severe response on challenge Aged under 16 FEV1 < than 70% predicted or greater than 1.5L 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 (...) test (  3mm) to Birch FEV1.> than 70% predicted or greater than 1.5L Aged 16 years or more Exclusion criteria Pregnancy Existing medical condition which could be affected by a severe response on challenge Aged under 16 FEV1.< than 70% predicted or greater than 1.5L On recruitment After a full explanation of the study given, patients who agree to participate will be asked to sign the consent form, a copy of which will be placed in the medical notes, and a second copy sent to the Ethics Committee

2007 Clinical Trials

12009. Spaced Versus Massed Skill Learning

: January 17, 2007 Study Completion Date : December 16, 2013 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 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 (...) lines, implanted medication pumps, blood vessel, cochlear or eye implants) with history of loss of consciousness or epilepsy with history of hyperthyroidism or individuals receiving drugs acting primarily on the central nervous system, which lower the seizure threshold such as antipsychotic drugs (chlorpromazine, clozapine) or tricyclic antidepressants. Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact

2007 Clinical Trials

12010. RCT of ChondroCelect® (in an ACI Procedure) vs Microfracture in the Repair of Cartilage Defects of the Knee

a reintervention of the index lesion - at 36 months. The index lesion is the lesion that was initially treated in the study. Safety: Adverse Events [ Time Frame: continuous up to 60 months ] Side effects are recorded as the number of patients with adverse events. These events are coded according to the Medical Dictionary for Regulatory Affairs (MedDRA terms). Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk (...) . Females of childbearing age should use a proven method to prevent pregnancy Exclusion Criteria: Participation in concurrent trials Participation in previous trials within 3 months Subjects with hepatitis, HIV or syphilis Malignancy Alcohol or drug (medication) abuse Poor general health as judged by Investigator Clinically relevant second cartilage lesion on the patella Patellofemoral cartilage lesion Osteochondritis Dissecans (OCD) : recent OCD (within 1 year before baseline), depth of lesion > 0.5cm

2006 Clinical Trials

12011. Clinical and Angiographic Outcomes With Hyperglycemic Control Post PCI

the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 18 Years to 90 Years (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: No Criteria Inclusion Criteria: Patients booked for catheter-based revascularization with balloon angioplasty and coronary stent placement Type II diabetes mellitus On 0-2 oral glucose lowering agents and able to double the dose of (or add) at least one glucose lowering agent. If HbA1c (...) Reduction of Hyperglycemia With Insulin Impact Restenosis and Improve Clinical Outcomes Following PCI? Study Start Date : July 2002 Study Completion Date : September 2005 Resource links provided by the National Library of Medicine available for: Arms and Interventions Go to Outcome Measures Go to Primary Outcome Measures : Volume of intimal hyperplasia in the stented segment by IVUS at 6 months following PCI Secondary Outcome Measures : Late loss in minimal luminal diameter of stented site in coronary

2006 Clinical Trials

12012. Imaging the Neurobiology of a Behavioral Treatment for Cocaine Dependence

contained within the body which may interfere with the MRI scan, as determined in consultation with a neuroradiologist and according to the guidelines set forth in the following reference book commonly used by neuroradiologists: "Guide to MR procedures and metallic objects" Shellock, PhD, Lippincott Williams and Wilkins, NY 2001. Lifetime exposure to radiation in the workplace, or history of participation in nuclear medicine procedures, including research protocols ** Positive Allen Test indicating lack (...) : Interventional (Clinical Trial) Actual Enrollment : 50 participants Allocation: Non-Randomized Intervention Model: Parallel Assignment Masking: None (Open Label) Primary Purpose: Treatment Official Title: Imaging the Neurobiology of a Behavioral Treatment for Cocaine Dependence Study Start Date : July 2006 Actual Primary Completion Date : July 2010 Actual Study Completion Date : January 2011 Resource links provided by the National Library of Medicine available for: Arms and Interventions Go to Arm

2006 Clinical Trials

12013. Progressive Intervention Program for Tinnitus Management

Description: The 2004 VA Annual Benefits Report reveals that tinnitus is the third most common individual service-connected disability in veterans. As of September 30, 2005, there were 339,573 veterans who had been awarded a service connection for their tinnitus, with annual compensation amounting to over $418,000,000 (Office of Policy and Planning, VA Central Office). In addition to being a major expense for VHA, tinnitus is a health care problem that is inadequately addressed at most VA medical centers (...) . We have developed a research-based model of tinnitus clinical management that is designed for efficient implementation in VA Audiology clinics. The objective of this study is to establish the model program at a VA Audiology clinic, and to evaluate its efficacy with veteran patients and its acceptability to audiologists. The study is based at the NCRAR, and a prototype tinnitus management program will be established in the Audiology Clinic at the James A. Haley (Tampa) VA Medical Center

2006 Clinical Trials

12014. Preventing Overweight in USAF Personnel: Minimal Contact Program

exercise. 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): NCT00417599 Locations Layout table for location information United States, Texas Wilford Hall Medical Center AFB San Antonio, Texas, United States, 78236 Sponsors and Collaborators Baylor College (...) in USAF Personnel: Minimal Contact Program 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: NCT00417599 Recruitment Status : Completed First Posted : January 1, 2007 Last Update Posted : June 24, 2016 Sponsor: Baylor College of Medicine Collaborator: United States Department of Defense Information provided

2006 Clinical Trials

12015. A Randomised, Comparing Fixed Doses of Pramipexole to Investigate the Efficacy and Safety in Patients With RLS.

of a state in which RLS symptoms begin to occur 2 hours earlier than the usual time zone for 5 days or more a week 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 (...) Study to Evaluate the Efficacy and Safety of Pramipexole at Fixed Doses of 0.25 mg, 0.5 mg, and 0.75 mg in Patients With Idiopathic Restless Legs Syndrome for 6 Weeks, Followed by a 46-week Open-label Long-term Study Study Start Date : October 2006 Actual Primary Completion Date : March 2008 Resource links provided by the National Library of Medicine related topics: related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Experimental: Pramipexole 0.25 mg once daily

2006 Clinical Trials

12016. Interviewing Children About Past Events: Evaluating the NICHD Interview Protocol

take off the costumes and the child will be told that he or she will receive the photographs at a later time. Another researcher posing as a photographer will come into the room, interrupting the event, and begin to argue with the first photographer about who had booked the equipment. They will resolve the argument and apologize to the child for the interruption. About 6 weeks after the event, the children will be interviewed using the ADAPTED VERSION OF NICHD interview protocol. Half (...) to the children involved, and we expect that both the staged event and the interviews will be enjoyable and stimulating. We expect that the results of the study will provide further support for the use of NICHD interview as a safe and effective means of interviewing children about past experiences. In addition to general information on children's eyewitness capabilities, the study is expected to supplement field studies by contributing knowledge about the accuracy of children's memory using the NICHD

2006 Clinical Trials

12017. Reading Preoperatively to Reduce Anxiety in Day Surgery

Primary Completion Date : June 2005 Actual Study Completion Date : April 2006 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: Treatment 50% randomized to receive treatment: reading pre-operatively Behavioral: Reading program Reading of children's story/picture books preoperatively No Intervention: Control 50% randomized to receive no intervention pre-operatively: no reading Outcome Measures Go to Primary (...) is designed to implement the reading of age appropriate books by a trained reader into the waiting area of a pediatric day surgery unit to determine if it is effective at reducing the anxiety and pain levels of parents and children by providing a safe and calming activity for the child. This is a single-centre trial based at the IWK Health Centre. The primary outcome will be based on the anxiety and pain scores of the research participants. Condition or disease Intervention/treatment Phase Pre-operative

2006 Clinical Trials

12018. Pilot Study of B-Type Natrieutic Peptide (BNP) Levels in Patients With Congenital Heart Disease(BNP)

Levels [ Time Frame: 1 day ] Levels of B-type naturietic peptide in the blood 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 (...) Last Update Posted : July 17, 2014 Sponsor: Emory University Collaborator: Pfizer Information provided by (Responsible Party): Wendy M. Book, Emory University Study Details Study Description Go to Brief Summary: The object of this study is to measure the levels of B-type Natriuretic Peptide (BNP) in patients with congenital heart disease, normal individuals, and patients with acquired heart failure, and compare the results from each group. Condition or disease Intervention/treatment Phase

2006 Clinical Trials

12019. Intravenous Saline Pre-Hydration in Patients Undergoing Outpatient Colonoscopy

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: Aged 18 or older Able to provide informed consent Booked for outpatient colonoscopy, where appointment has been generated by Gastroenterology Unit bookings staff. Exclusion Criteria: Booked for anaesthetist-supervised (...) 2 Detailed Description: Outpatient colonoscopy is a generally well-tolerated elective procedure. Colonoscopy completion rate is governed in part by patient comfort, which is enhanced by adequate sedation. In addition, comfort following colonoscopy determines timely recovery from the procedure and return to usual activities. Colonoscopy and sedation are frequently accompanied by hypotension (systolic blood pressure less than 100 mm Hg), which reduces the amount of sedation able to be employed

2006 Clinical Trials

12020. Effects of Beta-adrenergic in Adults w/Transposition of Great Arteries on Systemic Ventricular Function

: November 13, 2013 Sponsor: Emory University Information provided by (Responsible Party): Wendy M. Book, Emory University Study Details Study Description Go to Brief Summary: The purpose of this chart review study is to examine the effects of beta -adrenergic blocking agents on systemic ventricular dimensions, systemic atrioventricular valve function and exercise tolerance in patients with transposition of the great arteries (TGA) and systemic ventricular dysfunction. Condition or disease Congenital (...) Start Date : January 1997 Actual Primary Completion Date : March 2007 Actual Study Completion Date : March 2007 Resource links provided by the National Library of Medicine resources: Groups and Cohorts Go to Outcome Measures Go to Primary Outcome Measures : functional class [ Time Frame: 6 months to 5 years ] beta blockers improved functional class in patient's with transposition and systemic right ventricles Eligibility Criteria Go to Information from the National Library of Medicine Choosing

2006 Clinical Trials

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