statmate v.1.01i software (GraphPad Software Inc)
90
Structured Review
GraphPad Software Inc
statmate v.1.01i software
Statmate V.1.01i Software, supplied by GraphPad Software Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/statmate+v%2E1%2E01i+software/statmate+v+1+01i+software/pm40319829-51-7-7
Average 90 stars, based on 1 article reviews
Statmate V.1.01i Software, supplied by GraphPad Software Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/statmate+v%2E1%2E01i+software/statmate+v+1+01i+software/pm40319829-51-7-7
Average 90 stars, based on 1 article reviews
statmate v.1.01i software - by Bioz Stars,
2026-09
90/100 stars
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Sequencing:Article Title: Pharmacological interventions for the treatment of delirium in critically ill adults Article Snippet: Random sequence generation (selection bias) , Low risk , Participants were randomized by a clinical pharmacist in a 1:1 ratio via a Article Title: Pharmacological interventions for the treatment of delirium in critically ill adults Article Snippet: Haloperidol dose could be doubled every 24 hours until symptoms were controlled or the maximum dosage was attained Rescue medications were continued for 24 hours after a score of 0 was achieved on the ICDSC Assessment: s creening for subsyndromal delirium was done using the ICDSC, began 4 hours after extubation in the ICU, and was continued for every 8‐hour nursing shift thereafter, including after discharge to the cardiosurgical ward Non‐drug strategies: not reported Outcomes Primary (end of study) Incidence of delirium Secondary (end of study) Duration and severity of delirium Length of ICU and hospital stay Occurrence of adverse events (e.g. extrapyramidal symptoms) Notes Funding Support for the study was provided solely by institutional and/or departmental sources Registration No trial registration number was included in the manuscript Risk of bias Bias Authors' judgement Support for judgement Random sequence generation (selection bias) Low risk Participants were randomized by a clinical pharmacist in a 1:1 ratio via a Article Title: Pharmacological interventions for the treatment of delirium in critically ill adults Article Snippet: Bias Authors' judgement Support for judgement Random sequence generation (selection bias) Low risk Participants were randomized by a clinical pharmacist in a 1:1 ratio via a computer-generated random Article Title: Effect of early administration of inhaled heparin on outcomes of smoke inhalation injury: A randomized controlled trial. Article Snippet: Background: The present study aimed to examine the effects of early administration of inhaled heparin on the outcome of smoke inhalation injury.. Methods: Eighty-eight adults suffering smoke inhalation injury within 24 h were randomized to receive 5000 IU of heparin (n = 44) or normal saline (n = 44) by nebulization every 4 h until successful extubation or death, up to a maximum of 14 days.. The primary outcome was ventilator-free days (VFDs) and alive at 28 days. Selection:Article Title: Pharmacological interventions for the treatment of delirium in critically ill adults Article Snippet: Random sequence generation (selection bias) , Low risk , Participants were randomized by a clinical pharmacist in a 1:1 ratio via a Article Title: Pharmacological interventions for the treatment of delirium in critically ill adults Article Snippet: Haloperidol dose could be doubled every 24 hours until symptoms were controlled or the maximum dosage was attained Rescue medications were continued for 24 hours after a score of 0 was achieved on the ICDSC Assessment: s creening for subsyndromal delirium was done using the ICDSC, began 4 hours after extubation in the ICU, and was continued for every 8‐hour nursing shift thereafter, including after discharge to the cardiosurgical ward Non‐drug strategies: not reported Outcomes Primary (end of study) Incidence of delirium Secondary (end of study) Duration and severity of delirium Length of ICU and hospital stay Occurrence of adverse events (e.g. extrapyramidal symptoms) Notes Funding Support for the study was provided solely by institutional and/or departmental sources Registration No trial registration number was included in the manuscript Risk of bias Bias Authors' judgement Support for judgement Random sequence generation (selection bias) Low risk Participants were randomized by a clinical pharmacist in a 1:1 ratio via a Article Title: Pharmacological interventions for the treatment of delirium in critically ill adults Article Snippet: Bias Authors' judgement Support for judgement Random sequence generation (selection bias) Low risk Participants were randomized by a clinical pharmacist in a 1:1 ratio via a computer-generated random Article Title: Effect of early administration of inhaled heparin on outcomes of smoke inhalation injury: A randomized controlled trial. Article Snippet: Background: The present study aimed to examine the effects of early administration of inhaled heparin on the outcome of smoke inhalation injury.. Methods: Eighty-eight adults suffering smoke inhalation injury within 24 h were randomized to receive 5000 IU of heparin (n = 44) or normal saline (n = 44) by nebulization every 4 h until successful extubation or death, up to a maximum of 14 days.. The primary outcome was ventilator-free days (VFDs) and alive at 28 days. Software:Article Title: Pharmacological interventions for the treatment of delirium in critically ill adults Article Snippet: Random sequence generation (selection bias) , Low risk , Participants were randomized by a clinical pharmacist in a 1:1 ratio via a Article Title: Pharmacological interventions for the treatment of delirium in critically ill adults Article Snippet: Haloperidol dose could be doubled every 24 hours until symptoms were controlled or the maximum dosage was attained Rescue medications were continued for 24 hours after a score of 0 was achieved on the ICDSC Assessment: s creening for subsyndromal delirium was done using the ICDSC, began 4 hours after extubation in the ICU, and was continued for every 8‐hour nursing shift thereafter, including after discharge to the cardiosurgical ward Non‐drug strategies: not reported Outcomes Primary (end of study) Incidence of delirium Secondary (end of study) Duration and severity of delirium Length of ICU and hospital stay Occurrence of adverse events (e.g. extrapyramidal symptoms) Notes Funding Support for the study was provided solely by institutional and/or departmental sources Registration No trial registration number was included in the manuscript Risk of bias Bias Authors' judgement Support for judgement Random sequence generation (selection bias) Low risk Participants were randomized by a clinical pharmacist in a 1:1 ratio via a Article Title: Pharmacological interventions for the treatment of delirium in critically ill adults Article Snippet: Bias Authors' judgement Support for judgement Random sequence generation (selection bias) Low risk Participants were randomized by a clinical pharmacist in a 1:1 ratio via a computer-generated random Article Title: Effect of early administration of inhaled heparin on outcomes of smoke inhalation injury: A randomized controlled trial. Article Snippet: Background: The present study aimed to examine the effects of early administration of inhaled heparin on the outcome of smoke inhalation injury.. Methods: Eighty-eight adults suffering smoke inhalation injury within 24 h were randomized to receive 5000 IU of heparin (n = 44) or normal saline (n = 44) by nebulization every 4 h until successful extubation or death, up to a maximum of 14 days.. The primary outcome was ventilator-free days (VFDs) and alive at 28 days. |