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Superior Trunk Block Applied for Upper Arm Surgery

Investigation of the Effectiveness of Superior Trunk Block Applied for Upper Arm Surgery Operation Analgesia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05474014
Enrollment
60
Registered
2022-07-26
Start date
2022-07-20
Completion date
2023-12-01
Last updated
2024-01-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Operative Pain

Brief summary

Nerve blocks applied with ultrasonography are currently used for many post-operative pain and operations. Providing adequate area analgesia is the primary goal of clinicians, as early mobilization is suggested after shoulder and arm surgery. In this study aimed to investigate the effect of superior trunk block application on postoperative analgesic and motor functions.

Interventions

Local anesthetic injection will be applied to the superior trunk of the brachial plexus accompanied by ultrasonography.

Analgesics will be given using a patient-controlled analgesia device.

Sponsors

Bursa Yuksek Ihtisas Training and Research Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patients who were in the American Society of Anesthesiologists (ASA) I-III class * Underwent upper arm surgery

Exclusion criteria

* Previous local anesthetic allergy, * Having a bleeding diathesis disorder, * Mental disorder, * Allergic to the drugs used, * Patients who did not consent to participate in the study, * Presence of infection in the block area, * Patients with a body mass index above 30

Design outcomes

Primary

MeasureTime frameDescription
Visual Analog ScalePostoperative 24 hoursVisual Analog Scale was used for pain.Pain intensity was measured using 0-10 cm visual analogue scale (VAS). (0=no pain, 10=intolerable pain)

Secondary

MeasureTime frameDescription
tramadol consumption amountPostoperative 24 hourstramadol consumption amount with patient-controlled analgesia device
additional analgesic use amountPostoperative 24 hoursThe amount of paracetamol (intravenous, 1 g) or non-steroidal anti-inflammatory drug to be administered to patients with a Visuel analog scale above 5 after the operation.
postoperative complicationsPostoperative 24 hoursshortness of breath, hiccups, hoarseness
Horner syndromePostoperative 24 hoursHorner syndrome is a rare condition classically presenting with partial ptosis (drooping or falling of upper eyelid), miosis (constricted pupil), and facial anhidrosis (loss of sweating) due to a disruption in the sympathetic nerve supply

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026