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Estingpreviously documented cognitive testing, the WISC-IV, WNV, or another appropriate measure

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In addition, consent will be Rence in safety between the preoperative cylinder groups (P = 0.659, Mann- Whitney obtained from the parents and a cheekbrush sample will be collected for genetic analysis of the serotonin transporter PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/27196668 gene (SLC6A4). In addition, participant's levels of anxiety, anger/aggression, sadness/depression, excitability/overexcited, and ADHD were rated on a scale of 0 to 2 by the study doctor, psychologist, and/or research assistant. Following the second visit, the participant is randomized and study medication commencement is arranged.Post-treatment assessmentsParticipants in the study are required to meet the clinician on three occasions, two appointments for baseline assessment and one appointment to study sites for the post-trial assessment. During the first visit the study doctor will take a detailed medical history and conduct a physical examination. PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/25768400 For participants who do not haveTable 1 Summary of fluoxetine dosing schedule for participants <40 KgWeek of trial 1 2 3 4 5-16 17-20 Dose (per day) 4 mg 8 mg 14 mg 20 mg Maintain effective dose Wean off medication (at weekly intervals)At the completion of the 16-week treatment period, the participant and their parent(s) will be asked to return to the hospital for another study visit. During this visit ratings will be obtained for the CYBOCS-PDD, RBS-R, SCAS-parent version, ABC-community version, and the CGI. The participant's levels of anxiety, anger/aggression, sadness/depression, excitability/overexcited, and AD/HD were rated on a scale of 0 to 2 by the study doctor, psychologist, and/or research assistant. The participant is then weaned off the study medication over a four-week periodTable 2 Summary of fluoxetine dosing schedule for participants 40 KgWeek of trial 1 2 3 4 5-16 17-20 Dose (per day) 8 mg 14 mg 22 mg 30 mg Maintain effective dose Wean off medication (at weekly intervals)Mouti et al. Trials 2014, 15:230 http://www.trialsjournal.com/content/15/1/Page 6 ofand monitored weekly by either the research assistant or the study doctor.Treatment deliveryany given time should they be concerned about potential adverse side effects.Patient completion and withdrawalThe dosage schedule for the study medication, summarized in Tables 1 and 2, is based on previous research that highlights the importance of using lower doses and titrating doses slowly when treating children and adolescents with autism [13,28,29]. Dosages will be monitored using medication diaries provided to participants and their parents by the treating clinician. Participants will be given three medication diaries that outline the amount of medication to be taken at given periods: `Diary 1' for weeks 1 to 4, in which titration levels are increased; `Diary 2' for weeks 5 to 16, in which medication dosages are consistent and maintained; and `Diary 3' for weeks 17 to 22, in which medication is tapered. Parents are required to return each booklet at the required interval to monitor medication compliance.Monitoring, governance and wi.Estingpreviously documented cognitive testing, the WISC-IV, WNV, or another appropriate measure will be administered by a psychologist during the visit. In addition, consent will be obtained from the parents and a cheekbrush sample will be collected for genetic analysis of the serotonin transporter <a href="https://www.ncbi.nlm.nih.gov/pubmed/27196668" title=View Abstract(s)">PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/27196668 gene (SLC6A4).
asked خرداد 22 by turrethail9 (620 points)

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