search
Back to results

Intermittent Pneumatic Compression in Surgical Patients at Extremely-high Risk for Venous Thromboembolism (IPCSUPER)

Primary Purpose

Venous Thromboembolism, Venous Thrombosis

Status
Completed
Phase
Not Applicable
Locations
Russian Federation
Study Type
Interventional
Intervention
SCD
GCS
LMWH
Sponsored by
Pirogov Russian National Research Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Venous Thromboembolism focused on measuring venous thromboembolism, deep vein thrombosis, pulmonary embolism, prevention, intermittent pneumatic compression, sequential pneumatic compression, surgery, elastic compression, low-molecular weight heparin, prophylaxis

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age over 40
  • Major surgery undergone*
  • High risk of postoperative VTE according to a National guideline**
  • 11+ Caprini scores
  • Informed consent is given

Exclusion Criteria:

  • Acute deep vein thrombosis (DVT) at baseline
  • Performed inferior vena cava (IVC) plication or implanted IVC filter
  • Regular preoperative anticoagulation
  • Postoperative anticoagulation needed at therapeutic doses
  • Absence of anticoagulation for more than 5 days after surgery
  • Coagulopathy (not related to Disseminated intravascular coagulation syndrome)
  • Thrombocytopenia
  • Hemorrhagic diathesis
  • Lower limb soft tissue infection
  • Ankle-brachial index < 0.6

    • Major surgery - intervention under endotracheal anesthesia with duration of more than 60 min.

      • In accordance with a standard stratification system, high risk of VTE group includes patients over 60 years old after major surgery and patients 40-60 years old with additional risk factors after major surgery.

Sites / Locations

  • Clinical Hospital no.1 of the President's Administration of Russian Federation
  • Moscow Clinical Hospital no.24

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Experimental group (SCD + GCS + LMWH)

Control group (GCS + LMWH)

Arm Description

SCD: Intermittent pneumatic compression (IPC) with Kendall SCD™ Sequential Compression System 700 used continuously when the patient is in bed with 6-hours night interval free of compression: from 0 a.m. to 6 a.m. In the ICU SCD used continuously all day, and in surgery department - all time of bed resting. SCD used until discharge. GCS: Thigh-length graduated compression stockings with pressure of 18-21 mm. Hg at the ankle used all the time until discharge plus one month after discharge LMWH: LMWH enoxaparin (Clexane) 40 mg once a day subcutaneously started on 1st or 2-5th postoperative day according to the bleeding risk and used until discharge.

GCS: Thigh-length graduated compression stockings with pressure of 18-21 mm. Hg at the ankle used all the time until discharge plus one month after discharge LMWH: LMWH enoxaparin (Clexane) 40 mg once a day subcutaneously started on 1st or 2-5th postoperative day according to the bleeding risk and used until discharge.

Outcomes

Primary Outcome Measures

Number of Patients With Asymptomatic Venous Thrombosis of Lower Limbs as Detected by Duplex Ultrasound
Asymptomatic deep and/or superficial vein thrombosis of lower limbs detected by duplex ultrasound performed at baseline and then every 3-5 days after surgery until discharge.

Secondary Outcome Measures

Number of Patients With Proximal Deep Venous Thrombosis as Detected by Duplex Ultrasound
Proximal deep vein thrombosis defined as thrombus of popliteal, femoral, iliac veins and/or inferior vena cava. Detected by duplex ultrasound performed at baseline and then every 3-5 days after surgery until discharge.
Number of Patients With Isolated Calf Muscle Vein Thrombosis as Detected by Duplex Ultrasound
Isolated calf muscle vein thrombosis was defined as thrombosis of soleal, gastrocnemius or other calf muscle veins not extended into tibial, or peroneal, or popliteal veins. Detected by duplex ultrasound performed at baseline and then every 3-5 days after surgery until discharge.
Number of Patients With Pulmonary Embolism
Symptomatic pulmonary embolism (PE) that occurred during the inpatient period of treatment and confirmed by computed tomography pulmonary angiogram (CTPA) or single-photon emission computed tomography with computed tomography (SPECT/CT) or autopsy
Number of Patients Died From Any Reason
Inpatient postoperative mortality: number of patients died from any reason during the inpatient period of treatment
Number of Patients With Leg Skin Injury
Leg skin injury defined as any skin hyperemia, maceration, laceration, bubbles, erosion or ulceration in the zone of application for GCS and SCD on the lower limbs revealed by clinical inspection of the skin and soft tissues until discharge
Number of Patients With Symptomatic and Asymptomatic VTE Events at 30 Days After Surgery
Taking into account all VTE events: asymptomatic revealed by duplex ultrasound, symptomatic confirmed by duplex ultrasound, CTPA, SPECT/CT, autopsy in patients discharged from the hospital and still receiving inpatients care at 30 days after surgery.
Number of Patients Who Died From VTE at 30 Days After Surgery
VTE related deaths that occurred during inpatients and outpatient period of treatment and were confirmed by autopsy
Number of Patients With Symptomatic and Asymptomatic VTE Events at 180 Days After Surgery
Taking into account all symptomatic and asymptomatic VTE events confirmed by duplex ultrasound, CTPA, SPECT/CT, autopsy or other appropriate methods of diagnosis that occurred during the inpatient period of treatment and outpatient period of observation
Number of Patients Who Died From VTE at 180 Days After Surgery
VTE related deaths that occurred during inpatients and outpatient period of treatment and were confirmed by autopsy

Full Information

First Posted
February 1, 2017
Last Updated
January 13, 2021
Sponsor
Pirogov Russian National Research Medical University
Collaborators
Medtronic
search

1. Study Identification

Unique Protocol Identification Number
NCT03044574
Brief Title
Intermittent Pneumatic Compression in Surgical Patients at Extremely-high Risk for Venous Thromboembolism
Acronym
IPCSUPER
Official Title
Trial to Assess the Effectiveness of Intermittent Pneumatic Compression in the Prevention of Postoperative Venous Thromboembolism in Surgical Patients at Extremely High Risk
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
February 1, 2017 (Actual)
Primary Completion Date
September 30, 2018 (Actual)
Study Completion Date
December 31, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Pirogov Russian National Research Medical University
Collaborators
Medtronic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of the study is to evaluate efficacy and safety of venous thromboembolism prophylaxis by the combination of graduated compression stockings (GCS), standard doses of low-molecular-weight heparins (LMWH) and sequential compression device (SCD) in the mixed group of surgical patients at high and extremely high risk for venous thromboembolism.
Detailed Description
Venous thromboembolism (VTE) is the most common complication after major surgery, especially in high-risk patients. But the high-risk group is inhomogeneous. Some patients included in this group have an extremely high prevalence of postoperative venous thrombosis and pulmonary embolism, in whom the standard complex prophylaxis with elastic compression and standard anticoagulation is less effective. This is particularly so, in patients having a Caprini score of 11 and more, so that at the background of standard prophylaxis postoperative DVT is 10 times higher. This group of patients needs a more effective protocol for VTE prevention. Sequential compression devices (SCD) combined with graduated elastic compression stockings (GCS) or without them were found to be effective in the prevention of VTE in high-risk patients, especially after neurosurgical interventions, even without the administration of anticoagulants. However, their efficacy in patients at "extremely high risk", having 11+ Caprini scores has not been assessed yet. The aim of the current study is to evaluate efficacy and safety of VTE prophylaxis by the combination of graduated compression stockings (GCS), standard doses of low-molecular-weight heparins (LMWH) and sequential compression device (SCD) in the mixed group of surgical patients at high and extremely high risk for venous thromboembolism The expected outcome of the study is a reduction of asymptomatic postoperative venous thrombosis rate in the hospital and reduction in all VTE during 6 months after discharge.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Venous Thromboembolism, Venous Thrombosis
Keywords
venous thromboembolism, deep vein thrombosis, pulmonary embolism, prevention, intermittent pneumatic compression, sequential pneumatic compression, surgery, elastic compression, low-molecular weight heparin, prophylaxis

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A randomized clinical study to assess efficacy and safety of intermittent pneumatic compression device (SCD) application in combined prevention of postoperative VTE in surgical patients at high and extremely high risk receiving graduated compression stockings and early/delayed prophylactic anticoagulation with low-molecular weight heparins.
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
407 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Experimental group (SCD + GCS + LMWH)
Arm Type
Experimental
Arm Description
SCD: Intermittent pneumatic compression (IPC) with Kendall SCD™ Sequential Compression System 700 used continuously when the patient is in bed with 6-hours night interval free of compression: from 0 a.m. to 6 a.m. In the ICU SCD used continuously all day, and in surgery department - all time of bed resting. SCD used until discharge. GCS: Thigh-length graduated compression stockings with pressure of 18-21 mm. Hg at the ankle used all the time until discharge plus one month after discharge LMWH: LMWH enoxaparin (Clexane) 40 mg once a day subcutaneously started on 1st or 2-5th postoperative day according to the bleeding risk and used until discharge.
Arm Title
Control group (GCS + LMWH)
Arm Type
Active Comparator
Arm Description
GCS: Thigh-length graduated compression stockings with pressure of 18-21 mm. Hg at the ankle used all the time until discharge plus one month after discharge LMWH: LMWH enoxaparin (Clexane) 40 mg once a day subcutaneously started on 1st or 2-5th postoperative day according to the bleeding risk and used until discharge.
Intervention Type
Device
Intervention Name(s)
SCD
Intervention Description
Intermittent pneumatic compression (IPC) with Kendall SCD™ Sequential Compression System 700 used continuously when the patient is in bed with 6-hours night interval free of compression: from 0 a.m. to 6 a.m. In the ICU SCD used continuously all day, and in surgery department - all time of bed resting. SCD used until discharge.
Intervention Type
Device
Intervention Name(s)
GCS
Intervention Description
Thigh-length graduated compression stockings with pressure of 18-21 mm. Hg at the ankle used all the time until discharge plus one month after discharge
Intervention Type
Drug
Intervention Name(s)
LMWH
Intervention Description
LMWH enoxaparin (Clexane) 40 mg once a day subcutaneously started on 1st or 2-5th postoperative day according to the bleeding risk and used until discharge.
Primary Outcome Measure Information:
Title
Number of Patients With Asymptomatic Venous Thrombosis of Lower Limbs as Detected by Duplex Ultrasound
Description
Asymptomatic deep and/or superficial vein thrombosis of lower limbs detected by duplex ultrasound performed at baseline and then every 3-5 days after surgery until discharge.
Time Frame
time of discharge from the hospital or death, up to 45 days
Secondary Outcome Measure Information:
Title
Number of Patients With Proximal Deep Venous Thrombosis as Detected by Duplex Ultrasound
Description
Proximal deep vein thrombosis defined as thrombus of popliteal, femoral, iliac veins and/or inferior vena cava. Detected by duplex ultrasound performed at baseline and then every 3-5 days after surgery until discharge.
Time Frame
time of discharge from the hospital or death, up to 45 days
Title
Number of Patients With Isolated Calf Muscle Vein Thrombosis as Detected by Duplex Ultrasound
Description
Isolated calf muscle vein thrombosis was defined as thrombosis of soleal, gastrocnemius or other calf muscle veins not extended into tibial, or peroneal, or popliteal veins. Detected by duplex ultrasound performed at baseline and then every 3-5 days after surgery until discharge.
Time Frame
time of discharge from the hospital or death, up to 45 days
Title
Number of Patients With Pulmonary Embolism
Description
Symptomatic pulmonary embolism (PE) that occurred during the inpatient period of treatment and confirmed by computed tomography pulmonary angiogram (CTPA) or single-photon emission computed tomography with computed tomography (SPECT/CT) or autopsy
Time Frame
time of discharge from the hospital or death, up to 45 days
Title
Number of Patients Died From Any Reason
Description
Inpatient postoperative mortality: number of patients died from any reason during the inpatient period of treatment
Time Frame
time of discharge from the hospital or death, up to 45 days
Title
Number of Patients With Leg Skin Injury
Description
Leg skin injury defined as any skin hyperemia, maceration, laceration, bubbles, erosion or ulceration in the zone of application for GCS and SCD on the lower limbs revealed by clinical inspection of the skin and soft tissues until discharge
Time Frame
time of discharge from the hospital or death, up to 45 days
Title
Number of Patients With Symptomatic and Asymptomatic VTE Events at 30 Days After Surgery
Description
Taking into account all VTE events: asymptomatic revealed by duplex ultrasound, symptomatic confirmed by duplex ultrasound, CTPA, SPECT/CT, autopsy in patients discharged from the hospital and still receiving inpatients care at 30 days after surgery.
Time Frame
30 days
Title
Number of Patients Who Died From VTE at 30 Days After Surgery
Description
VTE related deaths that occurred during inpatients and outpatient period of treatment and were confirmed by autopsy
Time Frame
30 days
Title
Number of Patients With Symptomatic and Asymptomatic VTE Events at 180 Days After Surgery
Description
Taking into account all symptomatic and asymptomatic VTE events confirmed by duplex ultrasound, CTPA, SPECT/CT, autopsy or other appropriate methods of diagnosis that occurred during the inpatient period of treatment and outpatient period of observation
Time Frame
180 days
Title
Number of Patients Who Died From VTE at 180 Days After Surgery
Description
VTE related deaths that occurred during inpatients and outpatient period of treatment and were confirmed by autopsy
Time Frame
180 days
Other Pre-specified Outcome Measures:
Title
Duration of Inpatient Period of Treatment
Description
The inpatient period of treatment suggests time from surgical intervention to discharge from the hospital or death.
Time Frame
time of discharge from the hospital or death, up to 45 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age over 40 Major surgery undergone* High risk of postoperative VTE according to a National guideline** 11+ Caprini scores Informed consent is given Exclusion Criteria: Acute deep vein thrombosis (DVT) at baseline Performed inferior vena cava (IVC) plication or implanted IVC filter Regular preoperative anticoagulation Postoperative anticoagulation needed at therapeutic doses Absence of anticoagulation for more than 5 days after surgery Coagulopathy (not related to Disseminated intravascular coagulation syndrome) Thrombocytopenia Hemorrhagic diathesis Lower limb soft tissue infection Ankle-brachial index < 0.6 Major surgery - intervention under endotracheal anesthesia with duration of more than 60 min. In accordance with a standard stratification system, high risk of VTE group includes patients over 60 years old after major surgery and patients 40-60 years old with additional risk factors after major surgery.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kirill Lobastov, PhD
Organizational Affiliation
Pirogov Russian National Research Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinical Hospital no.1 of the President's Administration of Russian Federation
City
Moscow
ZIP/Postal Code
121352
Country
Russian Federation
Facility Name
Moscow Clinical Hospital no.24
City
Moscow
ZIP/Postal Code
127015
Country
Russian Federation

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32348101
Citation
Schastlivtsev I, Lobastov K, Barinov V, Kanzafarova I. Diosmin 600 in adjunction to rivaroxaban reduces the risk of post-thrombotic syndrome after femoropopliteal deep vein thrombosis: results of the RIDILOTT DVT study. Int Angiol. 2020 Oct;39(5):361-371. doi: 10.23736/S0392-9590.20.04356-4. Epub 2020 Apr 29.
Results Reference
result
PubMed Identifier
33201130
Citation
Lobastov K, Sautina E, Alencheva E, Bargandzhiya A, Schastlivtsev I, Barinov V, Laberko L, Rodoman G, Boyarintsev V. Intermittent Pneumatic Compression in Addition to Standard Prophylaxis of Postoperative Venous Thromboembolism in Extremely High-risk Patients (IPC SUPER): A Randomized Controlled Trial. Ann Surg. 2021 Jul 1;274(1):63-69. doi: 10.1097/SLA.0000000000004556.
Results Reference
derived

Learn more about this trial

Intermittent Pneumatic Compression in Surgical Patients at Extremely-high Risk for Venous Thromboembolism

We'll reach out to this number within 24 hrs