Skip to main content
OpenTrials
Completed

NCT Number: NCT05706090

Effect of Neurostimulator Usage on Block Success

The need of a neurostimulator for a successful nerve block was questioned in different block types after ultrasound has become standard. The aim of this clinical study was to determine the effect of neurostimulator use on block success in costoclavicular block

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Gazoosmanpasa Education and Research Hospital

Istanbul, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Class I, II and III of American Society of Anesthesiologists (ASA) classification
  • being between 18 and 80 years of age,
  • body mass index (BMI) between 18 and 35 kg/m2

Exclusion criteria

  • Patients who did not give consent,
  • were above ASA III,
  • pregnant,
  • had a neuromuscular disease,
  • bleeding diathesis,
  • a local anesthetic allergy,
  • an infection in the area where nerve block would be applied, and
  • had previously operated from the infraclavicular fossa were not included in the study

Treatment and study plan

fentanyl will be added

Drug

If adequate anagesia is not provided with the block, 1 microgram/kg of fentanyl will be added

General Anesthesia

Procedure

If adequate anagesia is not provided with the block, general anesthesia will be administered.

Primary outcomes

  1. The block success rate (ratio of successful blocks to all blocks)

    Time frame: during procedure

    The block was considered unsuccessful in case of analgesic need during the surgery or transition to general anesthesia, otherwise, these patients were included in the successful block group.

Secondary outcomes

  1. Block application time

    Time frame: 30 minutes

    THE TIME BETWEEN THE NEEDLE ENTRY THROUGH THE SKIN AND THE OUTPUT OF THE NEEDLE AFTER LOCAL ANESTHETICS IS GIVEN, WAS RECORDED AS THE APPLICATION TIME

  2. time to readiness for surgery

    Time frame: 30 minutes

    Sensory and motor block levels were evaluated in the median, radial, ulnar and musculocutaneous nerve traces at 5-minute intervals for 30 minutes. An ice pack was used for sensory block evaluation. It was scored as follows; 0: completely felt; 1: has a sense of touch; no cold; 2: no sense of touch. Lateral surface of the forearm for the musculocutaneous nerve, the surface of the thumb facing the palm for the median nerve, the inner surface of the 5th finger for the ulnar nerve, and the posterior surface of the hand for the radial nerve were used for sensorial evaluation. Motor block was scored as follows; 0: full motion; 1: paresis; 2: complete block. Elbow flexion for the musculocutaneous nerve, thumb opposition for the median nerve, 5th finger abduction for the ulnar nerve, and wrist extension for the radial nerve were used to evaluate motor block. The block was considered successful if the total score was 14 or higher, with a total sensory score of at least 7.

  3. number of needle passes

    Time frame: 30 minutes

    . The number of needle passes was calculated by adding each needle advancement exceeding 10 mm to the first needle insertion.

Sponsors and collaborators

Lead sponsor

Gaziosmanpasa Research and Education Hospital

Other Gov

Registry information

Official study title

Effect of Neurostimulator Usage on Block Success in Costoclavicular Block: a Randomized Controlled Trial

Important dates

Study start
2020
Primary completion
2020
Study completion
2021
First posted
Jan 31, 2023
Registry last updated
Jan 31, 2023

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.