Wound Infection Clinical Trial
Official title:
Efficacy of Negative Pressure Wound Closure Therapy by PICO System in Prevention of Complications of Femoral Artery Exposure
Evaluate negative pressure wound closure therapy by PICO system in Prevention of complications of femoral artery exposure.
INTRODUCTION:
Wound infection is a very common complication in patients who undergo femoral artery
exposure. It can lead to prolonged hospital stays, increased healthcare expenditures,
admission times, graft failure, and limb loss and is recognized as a significant cause of
postoperative morbidity and mortality.
Negative pressure wound therapy (NPWT) has been developped as a method for reducing the risk
of wound complications and is the wound dressing of choice in many vascular procedures during
the arterial exposure.
The idea of NPWT is a therapeutic technique wherein subatmospheric pressure is applied to a
wound using a sealed wound dressing that is connected to a vacuum pump, which can be
continuously or intermittently applied.
The mechanism of NPWT, is that it facilitates wound healing by decreasing the bacterial
burden; promoting granulation tissue formation, capillary blood flow, endothelial
proliferation, and angiogenesis; and restoring the integrity of the capillary basement
membrane.
The clinical efficacy of NPWT for closed incisions has been extensively studied in surgical
disciplines such as orthopedics, cardiothoracic, and plastic surgery, and its use in
promoting wound healing and improving patient outcomes has been validated. The use of
vacuum-assisted closure dressings (PICO system) is currently no evidenced that supports the
use PICO system of for lower limb femoral incisions. Therefore, we aimed to evaluate the
outcomes of PICO system in preventing wound complication in patients with femoral artery
exposure.
Aim of the work Evaluate negative pressure wound closure therapy by PICO system in Prevention
of complications of femoral artery exposure.
Outcome
Primary outcomes:
Infection Hematoma seroma
Secondary outcomes:
Wound Dehiscence. Patients and methods Study location: The study will be conducted at the
department of vascular surgery in Mansoura university hospitals Type of study: Randomized
controlled Prospective study Study duration: 2 years: 2019-2021 Sample size: 250 patients
n=(Z^2 p(1-p))/d^2 Where: Z= 1.96 at 95% confidence level, P= expected prevalence, d=
precision (margin of error)
Study population: The study will be conducted in all patients suspected to femoral artery
exposure whatever the type of surgery Inclusion criteria: all patients suspected to femoral
artery exposure whatever the type of surgery Exclusion criteria who can't give consent
(unconscious)? Those with mental or behavioral disorders will be excluded. Consent: Patients
after signing informed consent that possible complication from the procedure ought to happen
and what are the alternatives.
Data collection: The demographics, Symptoms and preoperative clinical data will be collected
History Data: included patient's demographics, underlying medical conditions, any previous
associated morbidity.
Examination: Arterial assessments. Laboratory: Blood picture, Blood sugar level, Kidney
functions, Liver functions and Coagulation profile.
Imaging: Duplex US and CTA Method of Randomization: Block randomization: Two elements A for
Application of the device, B for conventional dressing A A B B A B A B A B B A B B A A B A B
A B A A B Technique After closure of Femoral wound the PICO system is applied for up to 5-7
days. PICO® is a disposable, single-use pump without a canister that generates an effective,
non-adjustable, negative pressure of -80 mmHg and that can be used for up to 7 days.(-1113)
It incorporates leak detection and low battery indicators and is connected to a 4-layer
absorbent dressing that primarily removes wound exudates through evaporative loss. The
mechanism of action has been postulated to occur because of the combined effects of a
reduction in the frequency of dressing changes, a reduction in stress concentration in the
tissue surrounding the incision, and an enhancement in the appositional strength of the
incision line, thus reducing dead space and minimizing the risk of wound contamination.(14)
PICO® has also been demonstrated to enhance lymphatic clearance and decrease the risk of
hematomas or seromas(15) Follow up Every patient will be followed every week till first
month, then every 3 months till 1 years.
Hemodynamic improvement was assessed by ankle brachial pressure index (ABI), performed before
and after the procedure and every 3 months.
Evaluation made to determine wound complications (Infection, Hematoma, seroma and wound
dehiscence)
Statistical analysis The data will be analyzed using Statistical Package for the Social
Sciences. The numerical outcomes e.g. age is calculated as mean. Gender will be recorded as
frequency and percentage. Chi Square test is applied to assess the association of various
parameters. The results will be considered statistically significant if the p-value is found
to be less than or equal to 0.05.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT02905955 -
Vacuumtherapy After Venous Hybrid Procedures
|
Phase 4 | |
Not yet recruiting |
NCT02868372 -
Swabbing of Subcutaneous Tissues of Cesarean Section Wounds With Povidone Iodine
|
N/A | |
Enrolling by invitation |
NCT02559453 -
Outcomes for 2 Operations Versus ≥ 3 Operations in Infected Wounds
|
N/A | |
Completed |
NCT02744144 -
Wound Bacterial Microbiota and Their Antibiotic Resistance
|
N/A | |
Active, not recruiting |
NCT01939145 -
Comparing Outcomes for Prontosan Versus Normal Saline for Negative Pressure Wound Therapy With Instillation
|
Phase 4 | |
Completed |
NCT01141335 -
Polypropylene Mesh Versus Polytetrafluoroethylene (PTFE) Mesh in Inguinal Hernia Repair
|
Phase 4 | |
Completed |
NCT00998907 -
PDS*Plus and Wound Infections After Laparotomy
|
N/A | |
Terminated |
NCT00654641 -
Prevention of Wound Complications After Cesarean Delivery in Obese Women Utilizing Negative Pressure Wound Therapy
|
N/A | |
Completed |
NCT00576745 -
A Comparison Of The 3M TM S Surgical Skin Closure System To The Standard Vicryl Suture Closure of Sternotomy Incisions During Cardiac Surgery
|
Phase 1 | |
Completed |
NCT00402727 -
Comparison of Sequential IV/PO Moxifloxacin With IV Piperacillin/Tazobactam Followed by PO Amoxicillin/Clavulanic Acid in Patients With a Complicated Skin and Skin Structure Infection
|
Phase 3 | |
Recruiting |
NCT00150852 -
Prevention of Gastrostomy-Related Wound Infection by Vancomycin in Carriers of Methicillin-Resistant Staphylococcus Aureus.
|
Phase 2 | |
Not yet recruiting |
NCT03872544 -
Short Term Status of Free Dermal Fat Autografts for Complex Craniofacial Wounds
|
||
Recruiting |
NCT04596124 -
Effectiveness and Tolerability of Fitostimoline Plus Cream and Gauze vs Connettivina Bio Plus Cream and Gauze
|
N/A | |
Active, not recruiting |
NCT04584957 -
Prophylactic Negative Pressure Wound Therapy (VAC) in Gynecologic Oncology (G.O.)
|
N/A | |
Recruiting |
NCT03960970 -
Two-drug Antibiotic Prophylaxis in Scheduled Cesarean Deliveries
|
Phase 2 | |
Enrolling by invitation |
NCT03880188 -
Long Term Status of Free Dermal Fat Autografts for Complex Craniofacial Wounds
|
||
Completed |
NCT02018094 -
The Amputation Surgical Site Infection Trial (ASSIT)
|
Phase 4 | |
Terminated |
NCT03269968 -
Use of Negative Pressure Wound Therapy in Morbidly Obese Women After Cesarean Delivery
|
N/A | |
Enrolling by invitation |
NCT02945761 -
High Concentration of Sugar Solution Irrigation Promotes the Healing of Infected Wound
|
N/A | |
Not yet recruiting |
NCT02882360 -
Kerlix for Pregnant Women With Elevated BMI to Prevent Wound Infection by 6 Weeks Post Partum
|
Phase 4 |