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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03377985
Other study ID # FWA 000017585
Secondary ID
Status Completed
Phase N/A
First received December 7, 2017
Last updated December 17, 2017
Start date January 1, 2016
Est. completion date December 30, 2016

Study information

Verified date December 2017
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The current study focused on ultrasound guided brachial plexus block (BPB) which plays an important role in patients with hand trauma either in pain control or for surgical intervention. The brachial plexus can be blocked by several techniques but the most commonly used are the supraclavicular (SCB) and axillary (AXB) blocks. Aim of this study is to compare between the two techniques as regard performance time, needling time, anesthesia related time, block related complications, number of needle pass, and block related pain. 80 patients were allocated randomly into two equal groups, under ultrasound guidance the SCB and AXB were done for the two groups respectively. The needling time, performance time, anesthesia related time, onset time, number of 1st needle pass in each group and block related complications were noted.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date December 30, 2016
Est. primary completion date December 30, 2016
Accepts healthy volunteers No
Gender All
Age group 40 Years to 70 Years
Eligibility Inclusion Criteria:

- patients with ASA physical status II and III, and body mass index (BMI) between 20 and 35, aged 40-70, undergoing emergency crushed hand surgery

Exclusion Criteria:

- Patients with significant coagulopathy, infection or trauma at the injection site of local anesthetics, allergy to local anesthetics, refusal to participate, known neuropathies patients, mentally retarded patients, severely trauma patients who required general anesthesia from the start in the pre-induction room, and unconscious patients due to the accident. Also, shocked patients and patients with chronic obstructive airway disease

Study Design


Related Conditions & MeSH terms

  • Emergencies
  • the Study Focuses on Comparing Between Supraclavicular and Axillary Blocks

Intervention

Procedure:
brachial plexus block


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Outcome

Type Measure Description Time frame Safety issue
Primary block related complications failed block, motor weakness 24 h after the block, vascular puncture, Horner syndrome, paresthesia and pneumothorax 24 hours after the block
Secondary number of first needle pass how many times the needle is inserted till we can inject local anesthesia in a proper site 10-20 min