Effects of Angiotensin Converting Enzyme Inhibitors on Patency of Arterio-Venous Fistulas: A Randomized Controlled Trial
NCT ID: NCT05132712
Last Updated: 2021-11-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
EARLY_PHASE1
100 participants
INTERVENTIONAL
2021-10-01
2022-09-30
Brief Summary
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Patients of CKD often have associated cardiovascular diseases as Ischemic heart disease, left ventricular failure and angina. They are often taking cardio-protective medicines as antiplatelets, angiotensin converting enzymes and calcium channel blockers. Intimal hyperplasia has been shown to be the most important cause of AVF failures.2 Angiotensin II promotes vascular smooth muscle proliferation through various growth factors. Various experimental models have clearly depicted that ACE inhibitors effectively stop smooth muscle growth and intimal hyperplasia in vessel walls. Literature review shows conflicting results in terms of AVF patency when ACE inhibitors are used in conjunction. A study by Jackson RS and colleagues showed that ACE inhibitor were associated with reduced hazard ratio \[HR\], 0.35; 95% confidence interval \[CI\], 0.16-0.76; P = .008). Whereas, another study showed no role of ACE inhibitors in preventing graft failure. The possible explanation can be study designs as most studies were retrospective and effects of possible confounders. Moreover, there is lack of research in Pakistan to see the effects of pharmacological drugs on primary patency of AVF among CKD patients.
The rationale of this study is to effectively establish the role of ACE inhibitors in achieving primary patency of AV fistulas while reducing the number of confounders. This will be the first randomized controlled trial conducted in Pakistan. The primary outcome is AVF patency at one year. Secondary outcomes will include graft complications and graft maturation time after surgery.
Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Use of ACE inhibitor
losartan potassium will be administered 25 mg daily
Losartan Potassium
ACE inhibitor
placebo group
matched for age and gender
multi-vitamins
placebo drug
Interventions
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Losartan Potassium
ACE inhibitor
multi-vitamins
placebo drug
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* In patients who are not expected to start dialysis in next 3 months
* Non-consenting patients
* Patients with diagnosed carcinoma whose life expectancy is less than a year.
* Patients with un-controlled hypertension on multiple regimes of antihypertensive
* Patients allergic to ACE inhibitors
20 Years
79 Years
ALL
No
Sponsors
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Armed Forces Post Graduate Medical Institute (AFPGMI), Rawalpindi
OTHER
Responsible Party
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Ayesha Masood
Registrar vascular surgery
Locations
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Anas Bin Saif
Rawalpindi, Punjab Province, Pakistan
Countries
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Facility Contacts
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Anas Saif
Role: primary
Other Identifiers
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105471
Identifier Type: -
Identifier Source: org_study_id