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Effectiveness of Combined Anticoagulation and Antithrombotic Therapy vs Antithrombotic Therapy Alone After Lower Extremity Revascularization for Peripheral Arterial Disease

Primary Purpose

Combined Anticoagulation and Antithrombotic Therapy, PAD - Peripheral Arterial Disease

Status
Recruiting
Phase
Early Phase 1
Locations
Pakistan
Study Type
Interventional
Intervention
Rivaroxaban 10 MG Oral Tablet [Xarelto]
Sponsored by
Armed Forces Post Graduate Medical Institute (AFPGMI), Rawalpindi
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Combined Anticoagulation and Antithrombotic Therapy focused on measuring rivaroxaban in PAD

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

- all patients with PAD candidates for revascularization procedures

Exclusion Criteria:

  1. planned long-term dual antiplatelet therapy (>6 months),
  2. clinical requirement for therapeutic anticoagulation,
  3. recent acute limb ischemia or acute coronary syndrome,
  4. medical condition that could increase the risk of major bleeding, significantly impaired renal function at baseline (estimated glomerular filtration rate <15 mL•min-1•1.73 m-2),
  5. any documented history of intracranial hemorrhage, stroke, or transient ischemic attack

Sites / Locations

  • Combined Military HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Group A(combined anticoagulation plus antithrombotic therapy group)

Group B( antithrombotic therapy alone group)

Arm Description

group A patients would be receiving rivaroxaban and aspirin as experimental group to see the efficacy of rivaroxaban in peripheral arterial disease.

group B patients would be those receiving traditional antithrombotic therapy as usually given n Peripheral Arterial Disease.

Outcomes

Primary Outcome Measures

ALI
acute limb ischemia
major amputation for vascular reasons
any type of major amputation after revascularivation for PAD
MI
myocardial infarction
ischemic stroke
ischemic stroke
cardiovascular death
death because of cardiovascular events

Secondary Outcome Measures

thrombolysis in myocardial infarction(TIMI)major bleeding
combined therapy effect may result in increased bleeding tendency

Full Information

First Posted
July 30, 2021
Last Updated
April 29, 2022
Sponsor
Armed Forces Post Graduate Medical Institute (AFPGMI), Rawalpindi
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1. Study Identification

Unique Protocol Identification Number
NCT04994223
Brief Title
Effectiveness of Combined Anticoagulation and Antithrombotic Therapy vs Antithrombotic Therapy Alone After Lower Extremity Revascularization for Peripheral Arterial Disease
Official Title
Effectiveness of Combined Anticoagulation and Antithrombotic Therapy vs Antithrombotic Therapy Alone After Lower Extremity Revascularization for Peripheral Arterial Disease
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 2, 2021 (Actual)
Primary Completion Date
December 30, 2022 (Anticipated)
Study Completion Date
December 30, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Armed Forces Post Graduate Medical Institute (AFPGMI), Rawalpindi

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
EFFECTIVENESS OF COMBINED ANTICOAGULATION AND ANTITHROMBOTIC THERAPY VS ANTITHROMBOTIC THERAPY ALONE AFTER LOWER EXTREMITY REVASCULARIZATION FOR PERIPHERAL ARTERIAL DISEASE.
Detailed Description
Anticoagulation and antithrombotic therapy is a crucial part of PAD management as it prolongs the patecy of grafts in open surgical revascularization procedures so its proper dosage and duration without increasing risks to the patient and maximizing the benefits is very important. Currently literature in Pakistan regarding this problem couldn't be found so this study would help assessing the outcomes of anticoagulation and antithrombotic therapy in this population with respect to treatment options available and presentation variability of the peripheral arterial disease. Patients with PAD would be enrolled for 6 months and would be followed upto 12 months and then upto 24 months. Eligible subjects will be randomized 1:1 to receive either rivaroxaban 5 mg twice daily plus aspirin 75 mg once daily or rivaroxaban-matching placebo twice daily plus aspirin 75 mg once daily stratified by type of procedure; the treatment assignment will be double-blinded. Randomization and study treatment will begin as soon as possible but no later than 10 days after a successfull lower extremity revascularization. Patients will be prohibited from taking any additional antithrombotic therapy other drugs, including anticoagulants, doses of aspirin >100 mg daily, vorapaxar, ticagrelor, prasugrel, or cilostazol. Enrolled subjects will be having symptomatic PAD defined by evidence of an abnormal ankle-brachial index ≤0.80 in either limb with an anatomy of occlusive disease of involving segments. Subjects would be randomized who had undergone a technically successful endovascular, hybrid, or surgical LER within 10 days and had achieved adequate hemostasis before randomization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Combined Anticoagulation and Antithrombotic Therapy, PAD - Peripheral Arterial Disease
Keywords
rivaroxaban in PAD

7. Study Design

Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Model Description
patients enrolled in the study would be taken informed consent and divided in two groups, group A receiving rivaroxaban plus aspirin and Group B receiving placebo plus aspirin
Masking
ParticipantInvestigator
Masking Description
participants enrolled in the study and the principal investigator would not be knowing the drug regimens used in group A and Group B participants
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group A(combined anticoagulation plus antithrombotic therapy group)
Arm Type
Experimental
Arm Description
group A patients would be receiving rivaroxaban and aspirin as experimental group to see the efficacy of rivaroxaban in peripheral arterial disease.
Arm Title
Group B( antithrombotic therapy alone group)
Arm Type
Active Comparator
Arm Description
group B patients would be those receiving traditional antithrombotic therapy as usually given n Peripheral Arterial Disease.
Intervention Type
Drug
Intervention Name(s)
Rivaroxaban 10 MG Oral Tablet [Xarelto]
Intervention Description
rivaroxaban has shown improved results after revascularization for PAD in terms of limb survival
Primary Outcome Measure Information:
Title
ALI
Description
acute limb ischemia
Time Frame
upto 1 year
Title
major amputation for vascular reasons
Description
any type of major amputation after revascularivation for PAD
Time Frame
upto 1 year
Title
MI
Description
myocardial infarction
Time Frame
upto 1 year
Title
ischemic stroke
Description
ischemic stroke
Time Frame
upto 1 year
Title
cardiovascular death
Description
death because of cardiovascular events
Time Frame
upto 1 year
Secondary Outcome Measure Information:
Title
thrombolysis in myocardial infarction(TIMI)major bleeding
Description
combined therapy effect may result in increased bleeding tendency
Time Frame
2, 30, 180 and 365 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: - all patients with PAD candidates for revascularization procedures Exclusion Criteria: planned long-term dual antiplatelet therapy (>6 months), clinical requirement for therapeutic anticoagulation, recent acute limb ischemia or acute coronary syndrome, medical condition that could increase the risk of major bleeding, significantly impaired renal function at baseline (estimated glomerular filtration rate <15 mL•min-1•1.73 m-2), any documented history of intracranial hemorrhage, stroke, or transient ischemic attack
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ayesha masood, MBBS, FCPS Surgery
Phone
+923059159699
Email
laparoscopy.6@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Muhammad Irfan, MBBS,FCPS Surgery,
Phone
+923339259643
Email
irfan1373@yahoo.com
Facility Information:
Facility Name
Combined Military Hospital
City
Rawalpindi
State/Province
Punjab
ZIP/Postal Code
46000
Country
Pakistan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
muhammad jamil, MBBS, FCPS General Surgery
Phone
+923216409020
First Name & Middle Initial & Last Name & Degree
muhammad irfan, MBBS,FCPS Surgery
Phone
+923339259643
Email
irfan1373@yahoo.com

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
title
IPD Sharing Time Frame
6 months from start of study

Learn more about this trial

Effectiveness of Combined Anticoagulation and Antithrombotic Therapy vs Antithrombotic Therapy Alone After Lower Extremity Revascularization for Peripheral Arterial Disease

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