ULTRASOUND GUIDED INFRACLAVICULARY BLOCK FOR PAIN CONTROL AFTER UPPER EXTREMITY SURGERY

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

TCTR

Registry ID

TCTR20180814001

Enrollment

Unknown

Registered

2018-08-14

Start date

2015-07-01

Completion date

Unknown

Last updated

2026-03-30

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

Conditions

ultrasound&#45

Interventions

Ultrasound&#45

guided infraclavicular block with 30 mL of 0.25 % bupivacaine+fentanyl 50 mcg ,Ultrasound&#45

guided infraclavicular block with 30 mL of 0.25 % bupivacaine+fentanyl 100 mcg

Active Comparator Drug,Active Comparator Drug

Group I,Group II

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients admitted to the Department of Orthopedics and Traumatology of Fatih Sultan Mehmet Education and Research Hospital for elbow or forearm surgery between July 2015 - July 2016

Exclusion criteria

Exclusion criteria: Patients with a history of allergy to drugs used in the study, obesity (BMI> 35 kg/m2), patients using continuous narcotic analgesics due to chronic pain, upper extremity neurological dysfunction, infection along the injection site and coagulopathy

Design outcomes

Primary

Measure	Time frame
pain at admission to PACU, 15th-30th mn in PACU, po 2nd, 6nd 12th and 24 hours. Visual Analog Scale	—

Secondary

Measure	Time frame
first analgesic requirement time postoperative minute	—

Countries

turkey

Contacts

Public ContactDilek Ari

Fatih Sultan Mehmet Education and Research Hospital

dilekerdoganari@gmail.com905325429022

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026