Pecha Kucha-Based ERAS Education in Cardiovascular Surgery: Effects on Nursing Students' Knowledge and Attitudes
NCT07606144
ERAS, Nursing Students
Ankara, Söğütözü/Çankaya, Turkey (Türkiye)
View Trial DetailsNCT Number: NCT07242924
Cesarean section (CS) remains one of the most common major surgical procedures worldwide, with emergency CS accounting for approximately 30% of cases. Emergency CS presents unique challenges including increased maternal stress, higher complication rates, and prolonged recovery compared to elective procedures . Enhanced Recovery After Surgery (ERAS) protocols offer a promising approach to optimize outcomes in this population.
Originally developed for colorectal surgery, ERAS principles have been successfully adapted to obstetric practice over the past decade. These evidence-based protocols emphasize multimodal interventions including preoperative counseling, optimized analgesia, early mobilization, and timely nutrition. In obstetrics, ERAS implementation has demonstrated reduced length of stay, decreased opioid use, and improved patient satisfaction for elective CS .
Application of ERAS to emergency CS requires special considerations due to the urgent nature of the procedure. Modified protocols focus on rapid preoperative assessment, regional anesthesia with intrathecal opioids, and immediate postoperative care initiation . Emerging evidence suggests these adaptations maintain benefits while accommodating time constraints . Key outcomes include reduced postoperative pain, earlier return of bowel function, and improved breastfeeding rates .
Current research demonstrates ERAS protocols can be safely implemented in emergency CS with proper staff training and institutional support . Ongoing studies continue to refine optimal practices, particularly regarding fluid management and thromboprophylaxis . As evidence accumulates, standardized guidelines for emergency CS ERAS pathways are expected to emerge .
Trial opening soon.
Get Notified18 year–45 year
Female
Observational
The study is conducted on two phases. First phase study tools will be prepared. This is followed by the first and second audit cycles, preparatory phase is done to assess the intra-operative and post-operative care of women undergoing emergency cesarean section using the guidelines of Enhanced recovery after Surgery society. The quality of recovery score-11 translated into arabic. Permission is sought from adminstritive authorities.
First audit cycle : compliance with intraoperative measures is obtained by direct observation . post-operative information will be obtained by patient interview and record audit. The quiality of recovery will be assessed just before discharge using the quality of recovery score (ObsQoR-11).
Corrective action : gaps identified by first audit cycle is translated into defined corrrective measures.
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: From enrollment till discharge after 24 hours.
A data collection tool will be prepared for the study. After screening for eligibility, demographic factors, obstetric history. weight and gain, quality of previous cesarean scar if any, hemoglobin will be assessed for all patients. Observation of the outcomes will be recorded in the first phase of the study using a structured proforma and the Arabic version of ObQOR-11 score. Secondary outcomes measures include first oral intake, first abulation, first urination after catheter removal, passage of flatus and pain visual analog scale every 4 hours till discharge.
Time frame: During hospital stay up to discharge, typically within 24-48 hours postoperative
Time to first oral intake
Time frame: During hospital stay up to discharge, typically within 24-48 hours postoperative
Time to passage of flatus
Time frame: During hospital stay up to discharge, typically within 24-48 hours postoperative
Time to first ambulation
Time frame: During hospital stay up to discharge, typically within 24-48 hours postoperative
Time to first urination after catheter removal
Time frame: During hospital stay up to discharge, typically within 24-48 hours postoperative
Pain visual analog scale (VAS) scores every 4 hours until discharge
Assiut University
Other
Acronym: ERAS
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07606144
ERAS, Nursing Students
Ankara, Söğütözü/Çankaya, Turkey (Türkiye)
View Trial DetailsNCT07460310
Agnosia, Ankle (Ligaments); Instability (Old Injury)
View Trial DetailsNCT07017361
ERAS, Minimally Invasive Surgery
Daehak-ro, Jongno-gu, Seoul, South Korea
View Trial DetailsNCT06878079
ERAS, Gynecologic
View Trial Details