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Search / Trial NCT04921852

The Comparation of Lateral Sagittal Infraclavicular and Costoclavicular Block

Launched by ANKARA CITY HOSPITAL BILKENT · Jun 4, 2021

Trial Information

Current as of May 07, 2025

Unknown status

Keywords

Costoclavicular Block Lateral Sagittal Infraclavicular Block Brachial Plexus Block Block Onset Time

ClinConnect Summary

Participants between the ages of 18-70 with the American Society of Anesthesiology (ASA) score I-II-III will be included in the study. All participants will be evaluated preoperatively and information will be given about the anesthetic method to be applied. Demographic data and ASA scores of the participants will be recorded.

All of the participants included in the study will be taken to the regional anesthesia application room in the operating room approximately 1 hour before the operation. After standard anesthesia monitoring (electrocardiography, pulsoximetry, non-invasive blood pressur...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • American Society of Anesthesiologists physical status 1 to 3
  • 18-70 age
  • hand , wrist , forearm and elbow surgery
  • Exclusion Criteria:
  • refusal to participate,
  • pregnancy,
  • body mass index of 30 kg/m2 or greater
  • history of allergy to local anesthetic drugs
  • prior surgery over the infraclavicular fossa,
  • preexisting neurological deficit
  • coagulopathy
  • infection over infraclavicular fossa.

About Ankara City Hospital Bilkent

Ankara City Hospital Bilkent is a leading healthcare institution in Turkey, dedicated to advancing medical research and improving patient outcomes through innovative clinical trials. Equipped with state-of-the-art facilities and a multidisciplinary team of experienced professionals, the hospital fosters a collaborative environment for conducting rigorous scientific investigations. Its commitment to ethical standards and patient safety ensures that all clinical trials are conducted with the highest level of integrity, ultimately contributing to the development of new therapies and enhancing the quality of care provided to patients.

Locations

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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