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Study identifier: NCT07559942 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Effect of Apiban Therapy on AVF Maturation in ESRD Patients

Condition: Endstage Renal Disease · Direct Oral Anticoagulants (DOACs) · Arteriovenous Fistula  ·  Sponsor: Combined military hospital lahore

PhaseNA
Planned participants190
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

End-stage renal disease (ESRD) is a growing global health burden, and the creation of a native arteriovenous fistula (AVF) is the gold standard for vascular access in patients requiring hemodialysis \[1\]. AVFs offer superior longevity, fewer infectious complications, and lower mortality rates compared to central venous catheters or synthetic grafts \[2\]. However, a significant limitation to their widespread success is the high rate of early failure, primarily due to failure to mature (FTM). FTM occurs in 20-40% of AVFs, rendering them unusable for dialysis \[3\]. Apixaban, a direct factor Xa inhibitor, offers a potential advantage by providing sustained anticoagulation throughout the critical maturation period \[7\]. Its predictable pharmacokinetics, oral administration, and favorable safety profile make it an attractive agent for short-term use in this setting \[8\]. By reducing microthrombotic events during the first 4-6 weeks following AVF creation, apixaban could potentially improve maturation rates. However, this potential benefit must be weighed against the increased risk of bleeding, hematoma formation, and wound complications that could negatively impact fistula maturation \[9\].

This description comes directly from the study's public registry record.

Talk to the study team

Muhammad Kashif, FCPS Surgery  ·  00923219698888  ·  kashiramzan@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Combined Military Hospital, LahoreLahore, Punjab Province, PakistanRecruiting

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Source record: clinicaltrials.gov/study/NCT07559942