Perioperative/Postoperative Complications Clinical Trial
Official title:
Protocol for CAMUS Nurse Delphi Study: Active Involvement of Nursing Staff in Reporting and Grading Complication-Intervention Events - An Approach to Improve Patient Safety and Quality of Surgical Care
Multi-staged, international Nurse Delphi study that aims to validate the newly proposed CAMUS System and CAMUS CCI in an experienced nursing staff population.
Background: Comprehensive and reproducible assessment of post-operative complications are essential for reliable evaluation of quality of care and subsequent reformation of hospital safety infrastructure. At present, significant discrepancies exist in complication reporting and grading, and current complication systems lack holistic assessment of patient care by failing to consider and incorporate nursing insight and perception of patient burden. Objective: To gain experienced nursing perspective on current and future complication reporting and grading in Urology, validate the CAMUS-CCI, and quality control the use of the CDC in nurses. Design, Setting, and Participants: The 12 part REDCap-based Delphi survey was developed in conjunction with methodologist review, experienced nursing and urologist opinion. Certified local and international inpatient and outpatient nurses specialised in urology, perioperative nurses, and urology-specific advanced practice nurses/nurse practitioners will be included. A minimum sample size of 250 participants is targeted. Outcome Measurements and Statistical Analysis: The survey assesses participant demographics, nursing experience and opinion on complication reporting and the proposed CAMUS reporting recommendations, grading of intervention events using the existing Clavien-Dindo Classification and the proposed CAMUS Classification, and rating various clinical scenarios. Consensus will be defined as ≥75% agreement. If consensus is not reached, subsequent Delphi rounds will be performed under Steering Committee guidance. ;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Not yet recruiting |
NCT03994419 -
PErioperAtive CHildhood ObesitY
|
||
| Active, not recruiting |
NCT01681238 -
Goal-directed Therapy in High-risk Surgery
|
N/A | |
| Recruiting |
NCT05613439 -
The Fast-track Centre for Hip and Knee Replacement Database
|
||
| Recruiting |
NCT03740438 -
Modeling of the Hemoglobin Drop in the Uncomplicated Postoperative Course
|
||
| Completed |
NCT03269760 -
Multimodal Sleep Pathway for Shoulder Arthroplasty
|
Phase 1 | |
| Recruiting |
NCT05594199 -
Feasibility of a Virtual Smoking Cessation Program
|
N/A | |
| Completed |
NCT00538499 -
Fentanyl With or Without Bupivacaine in Reducing Pain in Patients Undergoing Video-Assisted Chest Surgery
|
N/A | |
| Recruiting |
NCT01690338 -
A Study of Residual Curarization Incidence in China
|
Phase 4 | |
| Recruiting |
NCT01110798 -
J-Pouch Colorectal Anastomosis or Straight Colorectal Anastomosis in Treating Patients With Rectal Cancer Who Have Undergone Surgery to Remove the Tumor
|
N/A | |
| Completed |
NCT00859157 -
Pain After Tumescent Mastectomy or Standard Mastectomy in Women With Stage I, Stage II, or Stage III Breast Cancer
|
N/A | |
| Withdrawn |
NCT03531268 -
Prospective Study to Evaluate the Clinical Utility of Perioperative Pharmacogenomic Testing
|
N/A | |
| Recruiting |
NCT04356638 -
a Phase III Trial of Safety and Efficacy of Premedication With Dexmedetomidine and Midazolam in Pediatric Patients
|
Phase 3 | |
| Completed |
NCT03579121 -
Genomic Opioid Optimization of Dosing and Selections (GOODS) Study
|
N/A | |
| Completed |
NCT03899441 -
Multimedia Aid Gynecologic Counseling and Consent
|
N/A | |
| Recruiting |
NCT06123039 -
Use of Heart-lung Interaction to Predict Haemodynamic Tolerance to the Open Lung Approach With Individualised PEEP
|
||
| Completed |
NCT01672892 -
Standard Versus Intensity-Modulated Pelvic Radiation Therapy in Treating Patients With Endometrial or Cervical Cancer
|
Phase 3 | |
| Completed |
NCT01510652 -
More Options Available With a Quadripolar LV Lead pRovidE In-clinic Solutions to CRT Challenges
|
N/A | |
| Completed |
NCT01680367 -
Wound Dressings For Split-Thickness Skin Graft Donor Sites in Patients Undergoing Surgery
|
N/A | |
| Active, not recruiting |
NCT00005600 -
Axillary Drainage Following Lymph Node Dissection in Women With Stage I or Stage II Breast Cancer
|
N/A | |
| Recruiting |
NCT05743673 -
SHAPE Test for Preoperative Risk Stratification
|