Perioperative/Postoperative Complications Clinical Trial
Official title:
The Impact of Advanced Age and High BMI on Short-term Outcomes in Live-donor Liver Transplant Recipients
Verified date | April 2023 |
Source | University of Pittsburgh |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Prospectively enrolled retrospective chart review and Liver Transplant database review to determine the modifiable and nonmodifiable risk factors specifically relating to Living Donor Liver Transplants. To observe the impact of age and BMI on graft outcomes and whether they impact the intraoperative management, post-operative length of stay, and complications.
Status | Completed |
Enrollment | 700 |
Est. completion date | November 30, 2022 |
Est. primary completion date | June 30, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - All patients who received a liver transplant at UPMC- Montefiore Hospital Age> 18 Exclusion Criteria: - Excludes Children (<18 years old) as they do not receive their operation under the same protocols Lost to follow-up prior to 1 year Participation in alternate research protocol that significantly altered the care they received in the perioperative period that may make their inclusion skew results. |
Country | Name | City | State |
---|---|---|---|
United States | UPMC Montefiore | Pittsburgh | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
University of Pittsburgh |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Graft Function 30 day | How well does the organ function | 30 day | |
Primary | Mortality | Mortality at 1 year | 1 year | |
Primary | Graft Survival 1 year | Survival of Organ at 1 year | 1 year | |
Secondary | Perioperative Complications | Any complications in the perioperative period | 30 day | |
Secondary | Length of Stay- Total and ICU | How long after surgery before patient is discharged from ICU and from Hospital | Up to 6 months | |
Secondary | Duration of Intubation/Ventilation | Time from Surgery End to Extubation or no longer requiring ventilatory support | Up to 6 months | |
Secondary | Postoperative Complications | Complications in the postoperative period- Renal, Infectious Disease, Pulmonary, Cardiac, Transplant related, Reintubation, Reoperation | Up to 6 months | |
Secondary | Blood Transfusion | Amount of blood transfusion required intraoperatively | Up to 2 days | |
Secondary | Vasoactive Medication | Amount and Type of Vasoactive Medication used at procedure end | Up to 2 days |
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
|