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#0 dbbase_sql->halt(Invalid SQL: select count(id) from dev_comment where pid='341313' and iffb='1') called at [/data/www/shop/includes/db.inc.php:54] #1 dbbase_sql->query(select count(id) from {P}_comment where pid='341313' and iffb='1') called at [/data/www/shop/comment/module/CommentContent.php:65] #2 CommentContent() called at [/data/www/shop/includes/common.inc.php:551] #3 printpage() called at [/data/www/shop/comment/html/index.php:13]
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Database error: Invalid SQL: select * from dev_comment where pid='341313' and iffb='1' order by id limit 0,10
MySQL Error: 1194 (Table 'dev_comment' is marked as crashed and should be repaired)
#0 dbbase_sql->halt(Invalid SQL: select * from dev_comment where pid='341313' and iffb='1' order by id limit 0,10) called at [/data/www/shop/includes/db.inc.php:54] #1 dbbase_sql->query(select * from {P}_comment where pid='341313' and iffb='1' order by id limit 0,10) called at [/data/www/shop/comment/module/CommentContent.php:167] #2 CommentContent() called at [/data/www/shop/includes/common.inc.php:551] #3 printpage() called at [/data/www/shop/comment/html/index.php:13]
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发布于:2019-4-18 22:13:54  访问:9 次 回复: 篇
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Of double-blind therapy with either GSK561679 or placebo inside a 1:1 manner.
Prior to randomization, subjects complete assessments of neuropsychological function, startle Tasocitinib citrate Biological Activity testing, and HPA axis sensitivity. Component 1 is usually a quick PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/26437915 checklist of 12 products that identifies potentially traumatizing events the patient has experienced, and Aspect two asks which of those events has troubled them most in the final month. Immediately after confirmation with all the study clinician, the trauma identified in Component two is determined to be the major trauma and applied as the concentrate in the ClinicianAdministered PTSD Scale (CAPS) [26], to monitor PTSD symptom severity and modify throu.Of double-blind remedy with either GSK561679 or placebo inside a 1:1 manner. Before randomization, subjects comprehensive assessments of neuropsychological function, startle testing, and HPA axis sensitivity. These measures are repeated after five weeks around the study medication to evaluate possible mediators and moderators of clinical alter. DNA for genotyping can also be collected. Following the six weeks of treatment, subjects enter a one month follow-up phase to monitor for security and durability of any clinical modifications. The study is getting performed in accord using the most up-to-date version in the Declaration of Helsinki [23]. Each and every site‘s Institutional Assessment Board (IRB) authorized the study design and style, procedures, and recruitment methods, with Emory University serving because the lead website (Emory University IRB, IRB number 00022717; Mount Sinai College of Medicine IRB, IRB number 04-0900 0001 03; Baylor College of Medicine IRB, IRB quantity H-30433 plus the Michael E DeBakey Veterans Affairs Medical Center Investigation and Development Plan, ID quantity 12G19. HBP; University of California San Francisco IRB, and the San Francisco Veterans Affairs Research and Improvement Committee, IRB number 12-09929). The study is registered at Clinicaltrials.gov: NCT01018992.Study participantsWomen 18 to 65 years old who meet Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV-TR) defined criteria for present PTSD of at least 3 months‘ duration are eligible. All interested subjects undergo phone screening to assess preliminary eligibility, and potentially eligible subjects are then scheduled for an in-office screening stop by. Subjects are paid US 50 for every single study visit, excluding the screening check out.Study sitesThe study is becoming performed at 4 academic web sites within the United states of america: Emory University, MSSM, BCM, and UCSF.Screening and remedy assessmentsThe schedule of assessments is presented in Table 1. Just after providing written informed consent, study participantsmeet using a staff member for an initial screening interview. The outcomes of this initial interview are then presented to a study psychiatrist, who confirms the PTSD diagnosis, evaluates exclusionary psychiatric diagnoses, and clarifies healthcare history and current remedy. Participants who stay eligible then total the Structured Clinical Interview for DSM-IV (SCID) [24] administered by a educated clinical interviewer. Demographic information on age, race, ethnicity, education level, marital status, employment status, and living situation are collected using a screening intake kind. Family psychiatric history is collected employing a self-report type listing major Axis I diagnoses and death from suicide. Simply because several patients with PTSD have skilled various traumas over their lifetime, it can be necessary to recognize the `index‘ trauma, defined as the trauma at the moment causing the greatest distress or impairment to the patient.
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