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Ankaferd Blood Stopper for Hemostasis After Transradial Coronary Angiography

Ankaferd Blood Stopper as a New Strategy to Avoid Early Complication After Transradial Coronary Angiography: A Randomized, Placebo-Controlled Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02982733
Enrollment
600
Registered
2016-12-05
Start date
2016-11-30
Completion date
2017-12-31
Last updated
2016-12-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Radial Artery Injury, Hematoma, Bleed

Brief summary

In 2008 Goker et al, introduced Ankaferd Blood Stopper (ABS) as a new hemostatic drug. Recently, ABS has been shown to produce local hemostasis by implementing topically after major arterial vessel injury. Reducing the compression time during patent hemostasis by facilitating hemostasis may decrease RAO. To test this hypothesis the investigators planned a three arm randomized study to evaluate the safety and efficacy of Ankaferd blood stopper in adjunct to short-time compression, compared to either short-time compression with conventional sterile gauzes or with a TR band after transradial diagnostic procedures.

Interventions

OTHERABS

Ankaferd Blood Stopper

DEVICETR Band

Transradial band

OTHERCS

Sterile Gauze

Sponsors

Acibadem University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All consecutive patients undergoing transradial elective diagnostic coronary procedures between November 2016 and November 2017 at the catheterization laboratory of Acibadem University Kocaeli Hospital were considered to be enrolled in the study.

Exclusion criteria

* The only

Design outcomes

Primary

MeasureTime frame
Radial artery occlusion assessed by reverse Barbeau's test24 hours

Secondary

MeasureTime frameDescription
Bleeding2 hoursany kind of bleeding defined as ml after the removal of hemostatic dressings or devices
Hematoma24 hourshematomas larger then \>5cm

Countries

Turkey (Türkiye)

Contacts

Primary ContactSevket Gorgulu, Prof
sevket5@yahoo.com02623174121

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026