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OpenTrials
Completed

NCT Number: NCT02614976

Incidences of Cuff-related Trauma After Noninvasive Blood Pressure Measurement Between With and Without Padding

Padding with cuff during blood pressure is expected to reduce number of skin crease or petechiae incidence.

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Key information

Conditions

Age range

19 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Siriraj hospital

Bangkoknoi, Bangkok, 10700, Thailand

About this study

Objective Primary Outcome : incidences of skin crease or petichiae after noninvasive blood pressure measurement ievery 5 minutes for 1 hour Secondary Outcome : factor related truma after noninvasive blood pressure measurement.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Health volunteer age > 18 or patients

Exclusion criteria

  • Peripheral vascular disease
  • Difference of blood pressure both arms > 15 mmHg
  • Acute dermal cappillary rupture
  • Phlebitis
  • Skin necrosis
  • Acute radial nerve injury
  • Deep vein thrombosis
  • Rumpel-Leede phenomenon
  • Compartment syndrome

Treatment and study plan

Padding

Device

Padding webrill (Covidian) TM 6"

Primary outcomes

  1. Complication of a non-invasive blood pressure cuff

    Time frame: 5 minutes after completion of non-invasive blood pressure measuring

    Petechiae and skin crease

Sponsors and collaborators

Lead sponsor

Siriraj Hospital

Other

Registry information

Important dates

Study start
2014
Primary completion
2017
Study completion
2018
First posted
Nov 25, 2015
Registry last updated
Feb 19, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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