Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
60 participants
INTERVENTIONAL
2020-02-01
2021-01-02
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
OTHER
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Group USP
The group using ultrasound and injection pressure manometer was named USP
fentanyl will be added
If adequate anagesia is not provided with the block, 1 microgram/kg of fentanyl will be added
general anesthesia
If adequate anagesia is not provided with the block, general anesthesia will be administered.
Group USPN
The group using ultrasound , injection pressure manometer , and neurostimulator was named USPN
fentanyl will be added
If adequate anagesia is not provided with the block, 1 microgram/kg of fentanyl will be added
general anesthesia
If adequate anagesia is not provided with the block, general anesthesia will be administered.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
fentanyl will be added
If adequate anagesia is not provided with the block, 1 microgram/kg of fentanyl will be added
general anesthesia
If adequate anagesia is not provided with the block, general anesthesia will be administered.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* being between 18 and 80 years of age,
* body mass index (BMI) between 18 and 35 kg/m2
Exclusion Criteria
* 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
18 Years
80 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Gaziosmanpasa Research and Education Hospital
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Döndü Genc Moralar
Associate Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Gazoosmanpasa Education and Research Hospital
Istanbul, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Neurostimulator Usage
Identifier Type: -
Identifier Source: org_study_id