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11941. A Comparison of Surgical Preparations and Wound Infection Rates for Elective Cesarean Sections

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: 19 Years and older (Adult, Older Adult) Sexes Eligible for Study: Female Accepts Healthy Volunteers: Yes (...) Criteria Inclusion Criteria: Age >19 years Gestational age > 37 weeks Booked elective cesarean section Exclusion Criteria: Gestational age < 37 weeks Premature rupture of membranes Onset of labor prior to procedure Evidence of maternal sepsis; maternal fever > 38.5C LSCS for emergency issues: non-reassuring fetal status, placental abruption, failed induction 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

11942. Effects of Fetal Movement Counting in Third Trimester of Pregnancy

and sense of control in interpretation of signals from own body and child, health promoting behavior [ Time Frame: One and a half year ] 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: 16 Years and older (Child, Adult, Older Adult) Sexes Eligible for Study: Female Accepts Healthy Volunteers: No Criteria Inclusion Criteria: women booking at screening ultrasound in pregnancy week 17-20 native speaking women singleton pregnancies Exclusion Criteria: women with pregnancies with severe anomalies or other cause to consider termination Contacts and Locations Go to Information from the National Library of Medicine

2007 Clinical Trials

11943. Foot and Ankle Edema Post-Cesarean Delivery

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: Child, Adult, Older Adult Sexes Eligible for Study: Female Accepts Healthy Volunteers: No Sampling Method: Probability Sample Study Population Pregnant women booked for an elective Cesarean delivery will be recruited into the study. Criteria Inclusion Criteria: Women (...) to investigate whether the size and shape of women's ankles do change following an elective cesarean delivery. We plan to investigate, if possible, the cause of any foot swelling after a cesarean whether it be the volume of intra venous fluids or oxytocin use. Condition or disease Foot and Ankle Edema Detailed Description: Pregnant women booked for an elective Cesarean delivery will be recruited into the study. Their foot volumes, based on volumetry, and foot and ankle circumferences will be measured prior

2007 Clinical Trials

11944. 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

11945. Non-Pneumatic Anti-Shock Garment for Obstetrical Hemorrhage: Zambia and Zimbabwe

by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment No Intervention: Control Clinics will collect data on patients experiencing shock due to obstetrical hemorrhage. In the control arm, half of the study clinics will not use the NASG but the NASG will be available at the referral hospital for patients transported there. Intervention Clinics will collect data on patients experiencing shock due to obstetrical hemorrhage. In the intervention arm, half (...) Outcome Measures : Mean amount of blood loss in mL , frequency of emergency hysterectomy, time to recovery from shock. [ Time Frame: during hospital stay ] Blood loss as measured by the blood collection drape at the RH or pad between SHF and RH. 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

2007 Clinical Trials

11946. 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

11947. An RCT to Evaluate Incidence, Cost and Clinical Outcomes Using 75 vs 100g. Screening Methods for Gestational Diabetes

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 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 (...) methodology. Outline: Pregnant women referred as outpatients for glucose testing for GDM will be given a study information sheet by obstetrics staff. At the time of booking the test they will be reminded of the study and to arrive fasting. On the day of glucose testing, the research assistant will invite patients to participate, obtain consent and perform randomisation into one three groups: (1) 50g screen ± 100g 3h GTT; (2) 50g screen ± 75g 2h GTT; or (3) 75g 2h GTT. During the glucose test, study

2006 Clinical Trials

11948. Family Lifestyle Overweight Prevention Program

functioning eating behaviors 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: 10 Years to 16 Years (Child) Sexes (...) Eligible for Study: All Accepts Healthy Volunteers: Yes Criteria Inclusion Criteria: Enrolled in the 6th or 7th grade at the target school. Parent consent and child assent to participate. Exclusion Criteria: Taking medications for weight control. 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

2007 Clinical Trials

11949. Genetic Studies in the Amish and Mennonites

History and other genealogy books ordatabases will be included in the AGDB. Outcome Measures Go to Primary Outcome Measures : Database [ Time Frame: Ongoing ] To maintain, expand, and use an electronic database containing the Anabaptist genealogies to facilitate the generation of pedigrees and calculation of common ancestors between nuclear families. Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk (...) A: Patients and their families with known or suspected Mendelian or complex traits, who will be enrolled in the molecular genetics and phenotypic characterization study. Informed consent will be obtained from each of these subjects. Group B: Those individuals who are listed in the Fisher Family History and multiple other genealogy books will be included in the AGD database. Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may

2006 Clinical Trials

11950. 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

11951. 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

11952. 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

11953. Preoperative Assessment for Synchronous Carcinoma or Polyps With Magnetic Resonance (MR) Colonography

Sponsor: Herlev Hospital Collaborator: University Hospital, Gentofte, Copenhagen Information provided by: Herlev Hospital Study Details Study Description Go to Brief Summary: The purpose of this study is to diagnose possible synchronous carcinomas and polyps with magnetic resonance (MR) colonography in patients booked for operation because of carcinoma in the descending or sigmoid colon, where a preoperative full colonoscopy is not possible. Two days before colonography, patients ingest a 200 ml (...) synchronous cancer or larger polyps Outcome Measures Go to Primary Outcome Measures : Feasibility of MR colonography to diagnose possible synchronous carcinomas and polyps [ Time Frame: 3 ] Secondary Outcome Measures : Altered operative strategy due to findings on MR colonography [ Time Frame: 3 ] 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

2006 Clinical Trials

11954. 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

11955. 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

11956. Pacemaker Therapy in Adults With Congenital Heart Defects

With Congenital Heart Defects 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: NCT00303511 Recruitment Status : Completed First Posted : March 17, 2006 Results First Posted : August 8, 2014 Last Update Posted : August 8, 2014 Sponsor: Emory University Information provided by (Responsible Party): Wendy M. Book (...) : Retrospective Official Title: Pacemaker Therapy in Adults With Congenital Heart Defects Study Start Date : January 1996 Actual Primary Completion Date : August 2006 Actual Study Completion Date : August 2006 Resource links provided by the National Library of Medicine related topics: Groups and Cohorts Go to Outcome Measures Go to Primary Outcome Measures : Feasibility of Pacemaker Implant With Total Thoracoscopic Approach to Epicardial Pacing Lead [ Time Frame: 30 days ] The ability to place a pacemaker

2006 Clinical Trials

11957. Effect of Cemented Stem Design on Periprosthetic Bone Mass Following Primary Total Hip Arthroplasty

provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 60 Years and older (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: No Sampling Method: Non-Probability Sample Study Population Pre-assessment clinics at Sheffield Hospitals, patients booked for hip replacements. Criteria Inclusion Criteria: patients must be aged 60 yrs or more uncomplicated primary or secondary osteoarthritis of the hip undergoing unilateral cemented (...) Completion Date : April 2011 Resource links provided by the National Library of Medicine related topics: related topics: Groups and Cohorts Go to Group/Cohort Intervention/treatment 1 C-stem implant Procedure: Total Hip Replacement Implantation of one of 3 stem designs 2 Charnley Implant Procedure: Total Hip Replacement Implantation of one of 3 stem designs 3 Exeter Implant Procedure: Total Hip Replacement Implantation of one of 3 stem designs Outcome Measures Go to Primary Outcome Measures : Proximal

2006 Clinical Trials

11958. 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

11959. 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

11960. 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

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