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Steri-strips for Reducing Radial Artery Compression Duration

Application of Steri-strips for Reducing the Duration of Post Procedure Radial Artery Compression Via Conventional Pneumatic Transradial Band: An Open-label Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04900987
Acronym
RACC
Enrollment
204
Registered
2021-05-25
Start date
2021-04-01
Completion date
2021-12-31
Last updated
2022-02-16

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

Conditions

Acute Coronary Syndrome

Keywords

Radial artery, TR Band, Steri-strips, Coronary angiogram, Radial patency

Brief summary

The duration of radial artery compression with the use of steri-strips may become much shorter than the duration of using the conventional pneumatic TR band alone for achieving hemostasis. Consequently, the frequency of radial artery occlusion (RAO) will be much lower and post procedure patency of radial artery will be higher along with significant alleviation of pain duration. Steri-strips is a kind of sterile adhesive tape used to approximate the clean and superficial wound or surgical incision as an alternate of stitch. Its ability to keep the radial puncture site incision approximated will lead to lesser chances of platelet plug disruption or displacement at the entry site and will hasten the process of hemostasis. The use of steri-strips unlikely to have adverse consequences as it is going to be used as an assist to the usual conventional method. In a study conducted by Faravash et al. in 2016, showed significant reduction in the area of post-rhinoplasty ecchymosis in lower lid, malar and cheek soft tissues with use of steri-strips with no reported safety concerns. Therefore, the aim of this study is to compare duration of radial artery compression by conventional method using the pneumatic TR band alone and with use of surgical steri-strips for achieving hemostasis with patency of radial artery after transradial coronary angiography along with reduction of pain duration due to arterial compression.

Detailed description

Study population: patients undergoing coronary angiography through transradial approach. Study groups: patients will be randomly assigned in a 1:1 manner to radial arterial compression with conventional pneumatic TR band alone and radial arterial compression with pneumatic TR band mechanical compression with use of clean sterile steri-strips. Treatment group. Pneumatic TR band compression with use of steri-strips Control group. Pneumatic TR band compression alone Method of radial artery compression after sheath removal: Conventional mechanical compression: Application of pneumatic TR band alone for 4 hours. Mechanical compression with use of steri-strips: After putting adequate manual pressure proximal to radial puncture site, dry and sterile application of steri-strip followed by pneumatic TR band for 1 hour. END POINTS: Primary endpoint will be the time duration of achieving hemostasis with radial artery patency Secondary endpoint will be Hematoma or Bleeding

Interventions

Pneumatic TR band compression with use of steri-strips

Sponsors

National Institute of Cardiovascular Diseases, Pakistan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

patients will be randomly assigned in a 1:1 manner to radial arterial compression with conventional pneumatic TR band alone and radial arterial compression with pneumatic TR band mechanical compression with use of clean sterile steri-strips.

Eligibility

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

Inclusion criteria

* Patients undergoing coronary angiography through transradial approach * Either gender with age ≥18 years * Positive Barbeau test (type A to C)

Exclusion criteria

* Patients refuse to give consent * Negative Barbeau test (type D) * Patients with bleeding diathesis or on oral anticoagulation

Design outcomes

Primary

MeasureTime frameDescription
Mean ofImmediately after removal of TR bandTime duration of achieving hemostasis
Number of Participants withAfter 24 hour of removal of TR bandRadial artery patency

Secondary

MeasureTime frameDescription
Number of Participants withImmediately after removal of TR bandHematoma

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026