CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 177 enrolled
Drug / intervention
Donor pain managementbehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02073435
NCT02073435N/ACompleted

A2ALL-Patients Safety System Improvements in Living Donor Liver Transplant

Northwestern University·observational·Posted Feb 27, 2014·Updated Dec 5, 2018

In Brief

An observational study evaluating Donor pain management for Liver Diseases and 3 related conditions. Completed, enrolled 177 participants across 4 sites.

Detailed Summary

Living donor liver transplantation (LDLT), involves complex systems and processes of care that are particularly vulnerable to medical errors and preventable complications. This ancillary study of the Adult-to-Adult Living Liver Transplantation Cohort Study (A2ALL) will focus on conducting a proactive, systematic, and comprehensive assessment of the vulnerabilities in the systems and process of LDLT care to reduce medical errors and preventable complications thereby improving the safety of LDLT care. This project will address an important gap in the knowledge needed to achieve high quality and safe LDLT care of patients by developing a process to: 1) proactively, systematically and comprehensively identify areas of vulnerabilities in LDLT care that can result in medical errors, 2) design and implement solutions to mitigate these weaknesses, and 3) evaluate the effectiveness of these solutions to improve the safety of LDLT care by measuring clinical and process outcomes before and after solution implementation across four A2ALL participating transplant centers

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedFeb 27, 2014
Enrollment StartOct 1, 2010
Primary CompletionMay 1, 2015
Study CompletionApr 1, 2018
TodayJul 2, 2026
Enrollment to primary: 4.6 yearsPosted 12.3 years ago

Interventions

Donor pain managementbehavioral

The evidence-based donor pain management solution entails the following elements: Preoperative Assessment and Management: * Assessment of Patient Risk factors for Respiratory Depression (e.g. OSA Assessment: STOP BANG Questionnaire) * Bowel preparation (e.g. Colace or Golytely) * Patient Postoperative Pain Education - Educational handout on postoperative pain At the end of the case in OR: * Local Anesthetic (TAP block, OnQ device, intrathecal, local infiltration) * I.V. Ketorolac (when adequate hemostasis is determined by surgeon and urine output is \> 500cc) * I.V. Steroids (Dexamethasone or Solumedrol) Postoperative Management: * NSAIDS x 72 hours followed by po cox-inhibitor until discharge (e.g. Celecoxib) * Opioids (Dilaudid PCA followed by oral opioids (e.g., Tylenol #3)) Postoperative Assessment: o CO2 monitoring in PACU/ICU for early monitoring of respiratory depression