- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03996668
Effect of Compression Stockings on Cerebral Desaturation Events in Obese Patients Undergoing Shoulder Arthroscopy in the Beach Chair
June 21, 2019 updated by: Nickolas Garbis, Loyola University
The Effect of Compression Stockings on Cerebral Desaturation Events in Obese Patients Undergoing Shoulder Arthroscopy in the Beach Chair Position - A Randomized Prospective Study
The study compares the effect of thigh high compression stockings on cerebral desaturation events in patients undergoing shoulder arthroscopy in the beach chair position with a BMI greater than or equal to 30.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
On the day of surgery, enrolled patients whom have signed consent for participation in the study will be randomized to receive thigh high compression stockings with SCDs or SCDs alone.
The importance of the investigation, proposed methodology, and potential risks of participation will be addressed.
In the pre-operative holding area, a cerebral oximeter (INVOS 5100C, Covidien) will be placed on the skull as directed by the manufacturer.
The sensors will be placed on the skull bilaterally in order to assess perfusion in both hemispheres.
Cerebral oximeter is a non-invasive, transcutaneous tool that can be used to measure cerebral tissue oxygenation.
The tool uses nearinfrared spectroscopy to measure the percentage of hemoglobin saturated with oxygen in the microcirculation of tissue within approximately 2-3cm below the skin.
The technology is approved by the FDA in the anesthesia setting to monitor cerebral oxygenation and is commonly used in cardiothoracic surgery and its use has been validated in the surgical setting.11
A baseline cerebral tissue oxygen saturation (rSO2) will be recorded.
All patients will be anesthetized using a standardized protocol.
Once anesthesia has been induced, thigh high compression stockings will be applied to the appropriate group followed by SCDs.
All patients in the study will wear sequential compression devices on both legs for thrombosis prophylaxis regardless of randomization.
The patient will then be raised into the beach chair position and secured in the normal fashion and the planned surgery will begin.
Intraoperative rSO2 data will be continuously recorded throughout the case.
The system will be set to alarm when the rSO2 decreases greater than 20% from baseline.
These events will be recorded throughout the case as CDEs.
To avoid cerebral vascular injury, these events will be treated with a protocol by anesthesia including ephedrine, phenylephrine, and the patient may be returned to the supine position if needed.
When surgery is complete, patients will be recovered in the post-anesthesia care unit.
The study will be conducted at three facilities within the Loyola system: the Loyola Ambulatory Surgery Center at Oakbrook (LASCO), the Ambulatory Surgery Center at Loyola (ASC), and at Gottlieb Memorial Hospital (GMH).
Personnel will include the attending surgeon, orthopaedic surgery residents, and anesthesia staff assigned to each case, all of whom will be fully educated on the study and protocols.
Study Type
Interventional
Enrollment (Actual)
66
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Illinois
-
Maywood, Illinois, United States, 60153
- Loyola University Medical Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
• All patient over age 18
- BMI > 30
- Undergoing shoulder arthroscopy in beach chair position
Exclusion Criteria:
• Age < 18 years
- BMI < 30
- Known and documented >90% occlusion of carotid artery
- Prior neck surgery
- Women who are pregnant
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control
Subjects received standard operating room dress including sequential compression devices.
|
|
|
Experimental: Experimental
Subjects wore thigh high compression stockings in addition to standard operating room dress including sequential compression devices.
|
Thigh high compression stockings will be placed after induction of anesthesia and intubation.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cerebral Desaturation Events
Time Frame: Intraoperative measurement that begins the with upright positioning and ends with return to supine positioning. There are no postoperative measures.
|
Intraoperative Cerebral desaturation events is defined as a decrease of 20% or more in cerebral oxygenation percentage from a preoperative supine baseline and is measured by Near Infrared Spectroscopy
|
Intraoperative measurement that begins the with upright positioning and ends with return to supine positioning. There are no postoperative measures.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Nickolas Garbis, MD, Loyola University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Fischer GW, Torrillo TM, Weiner MM, Rosenblatt MA. The use of cerebral oximetry as a monitor of the adequacy of cerebral perfusion in a patient undergoing shoulder surgery in the beach chair position. Pain Pract. 2009 Jul-Aug;9(4):304-7. doi: 10.1111/j.1533-2500.2009.00282.x. Epub 2009 Mar 17.
- Pohl A, Cullen DJ. Cerebral ischemia during shoulder surgery in the upright position: a case series. J Clin Anesth. 2005 Sep;17(6):463-9. doi: 10.1016/j.jclinane.2004.09.012.
- Salazar D, Sears BW, Aghdasi B, Only A, Francois A, Tonino P, Marra G. Cerebral desaturation events during shoulder arthroscopy in the beach chair position: patient risk factors and neurocognitive effects. J Shoulder Elbow Surg. 2013 Sep;22(9):1228-35. doi: 10.1016/j.jse.2012.12.036. Epub 2013 Feb 15.
- Papadonikolakis A, Wiesler ER, Olympio MA, Poehling GG. Avoiding catastrophic complications of stroke and death related to shoulder surgery in the sitting position. Arthroscopy. 2008 Apr;24(4):481-2. doi: 10.1016/j.arthro.2008.02.005.
- Kwak HJ, Lee JS, Lee DC, Kim HS, Kim JY. The effect of a sequential compression device on hemodynamics in arthroscopic shoulder surgery using beach-chair position. Arthroscopy. 2010 Jun;26(6):729-33. doi: 10.1016/j.arthro.2009.10.001. Epub 2010 Mar 3.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 1, 2018
Primary Completion (Actual)
March 1, 2019
Study Completion (Actual)
March 1, 2019
Study Registration Dates
First Submitted
June 11, 2019
First Submitted That Met QC Criteria
June 21, 2019
First Posted (Actual)
June 25, 2019
Study Record Updates
Last Update Posted (Actual)
June 25, 2019
Last Update Submitted That Met QC Criteria
June 21, 2019
Last Verified
June 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 209868
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
IPD will not be shared
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Obese
-
King's College LondonGuy's and St Thomas' NHS Foundation TrustCompleted
-
National Science and Technology Council, TaiwanMinistry of Science and Technology, Taiwan; Fondation FondaMental; Fondation...Recruiting
-
Ain Shams UniversityNot yet recruitingBleeding | Obese Patients | Obese Patients With Bariatric SurgerySaudi Arabia
-
Second Affiliated Hospital, School of Medicine,...Completed
-
Aphaia Pharma US LLCRecruitingObese Patients (BMI ≥ 30 kg/m²) | Obese With ComorbiditiesGeorgia
-
Yongxin ZhouNot yet recruiting
-
Universitas PadjadjaranCompleted
-
University Hospital, GhentCompleted
-
University of AvignonInstitut Saint PierreRecruitingDiet Modification | Exercise | Dietary Supplement | Obese AdolescentsFrance
Clinical Trials on Thigh High Compression Stockings
-
Loyola UniversityCompletedObesity | Shoulder ImpingementUnited States
-
University of Maryland, BaltimoreNational Institute on Aging (NIA); University of Texas Southwestern Medical...RecruitingVenous Insufficiency | Leg Edema | Venous Ulcers | Heart Failure,CongestiveUnited States
-
University of WashingtonLake Washington Vascular; Sigvaris, IncUnknownVaricose VeinsUnited States
-
Imperial College LondonNational Institute for Health Research, United KingdomRecruitingSurgery | Venous ThromboembolismUnited Kingdom
-
Karbala UniversityCompleted
-
University Hospital ErlangenCompletedVascular Diseases | Vascular Malformations | Venous Malformation | Vascular Malformation PeripheralGermany
-
Federal University of São PauloUnknownQuality of Life | Cellulitis
-
Seçil YavaşCompletedMaternal Hypotension Associated With Spinal Anesthesia During Cesarean SectionTurkey (Türkiye)
-
Belarusian State Medical UniversityCompleted
-
University of Sao PauloFundação de Amparo à Pesquisa do Estado de São PauloCompletedObstructive Sleep Apnea | Renal Failure Chronic Requiring DialysisBrazil