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OpenTrials
Completed

NCT Number: NCT04943367

Effect of TEAS on Rocuronium Injection Pain

Pain from the injection of rocuronium is a common side effect during anesthetic practice, occurring in 50%-80% of patients. Several methods have been used to reduce this pain. This prospective, randomized study was designed to determine the efficacy of transcutaneous electrical acupuncture point stimulation in reducing the rocuronium injection pain.

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Betul Kozanhan

Konya, 42005, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • 18-65 year aged
  • ASA I-III
  • Who was to undergo various elective operations.

Exclusion criteria

  • Cardiovascular surgery
  • Patients with pacemakers
  • Patients requiring rapid sequential induction

Treatment and study plan

TEAS

Device

Transcutaneous electrical acupuncture stimulation

Primary outcomes

  1. Pain with rocuronium injection

    Time frame: 5 minutes

    pain will be graded as no pain; mild pain; moderate pain; severe pain following administration of a priming dose of rocuronium

Sponsors and collaborators

Lead sponsor

Konya Meram State Hospital

Other

Registry information

Official study title

Efficacy of TEAS On Prevention of Rocuronium Injection Pain

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Jun 29, 2021
Registry last updated
Jan 6, 2022

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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