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Clinical Trials in Egypt / NCT07028957
Active, not recruiting Not applicable

Effectiveness of Low Volume Versus High Volume of Local Anesthetic in Ultrasound Guided Combined Supraclavicular and Interscalene Block for Upper Limb Surgery

NCT07028957 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-06-30
Last updated
2025-07-23

Condition(s) studied

Analgesia, PostoperativeComplications of Treatment

Investigational drug(s) / intervention(s)

Group A; Low volume local anesthetic in Ultrasound guided combined Supraclavicular and Interscalene block for Upper limb surgeryGroup B; High volume local anesthetics (30-40ml) ultrasound guided combined Supraclavicular Block (SCB) and Interscalene Block (ISB)

Group A; Low volume local anesthetic in Ultrasound guided combined Supraclavicular and Interscalene block for Upper limb surgery: Group A; will receive ultrasound guided combined Supraclavicular Block (SCB) with 7-10 ml (3.5-5 ml bupivacaine 0.5% plus 3.5-5 ml lidocaine 2%) and Interscalene Block (ISB) with 7-10 ml (3.5-5 ml bupivacaine 0.5% plus 3.5-5 ml lidocaine 2%).

Group B; High volume local anesthetics (30-40ml) ultrasound guided combined Supraclavicular Block (SCB) and Interscalene Block (ISB): Group B; High volume local anesthetics in ultrasound guided combined Supraclavicular Block (SCB) with 15-20 ml (7.5-10ml bupivacaine 0.5% plus 7.5-10 ml lidocaine 2%) and Interscalene Block (ISB) with 15-20 ml (7.5-10 ml bupivacaine 0.5% plus 7.5-10 ml lidocaine 2%).

Study summary

The aim of this study is to evaluate the effectiveness of low versus high volumes of local anesthetic in ultrasound-guided combined supraclavicular block (SCB) and interscalene block (ISB) for upper limb surgery. This randomized, controlled trial will assess the analgesic effectiveness of low-volume local anesthetic in these blocks.

We hypothesize that a low volume will provide similar analgesic effects to a high volume, with fewer complications. The study will involve 40 adult ASA I and ASA II patients undergoing upper limb surgery, divided into two groups: Group A (low volume) and Group B (high volume).

The primary outcome will compare intraoperative and postoperative analgesic effects of different volumes.

The secondary outcome will evaluate complications related to local anesthetics (toxicity) and injection techniques (e.g., phrenic nerve palsy, pneumothorax, hematoma).

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Patients aged 18 to 65 of both sexes * ASA classification I or II * Scheduled for upper limp surgery * Will be randomized 1:1 into two groups; group A; low volume local anesthetics (15-20ml) and group B; high volume local anesthetics (30-40 ml). Exclusion Criteria: * Patients who refuse participation. * Have allergies to local anesthetics. * Phrenic nerve dysfunction. * Chronic opioid use. * ASA III or higher classification. * Coagulopathy (bleeding disorders with INR \> 1.5 and/or platelets \< 50 000) * Severe chronic obstructive pulmonary disease. * Local infection at the injection site

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Souad Kafafi University Hospital (SKUH), faculty of medicine, Misr University for Science and Technology (MUST) Giza Giza Governorate

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07028957 on ClinicalTrials.gov ↗ ← All trials in Egypt