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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04729868
Other study ID # aswu/125/4/17
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2017
Est. completion date October 1, 2020

Study information

Verified date January 2021
Source Aswan University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate the efficacy of levo-bupivacaine alone and with dexmedetomidine in Ultrasound guided infraclavicular brachial plexus block for hand and forearm surgeries as regard: Onset of sensory and motor blockade. Duration of sensory and motor blockade. Analgesic pain scores using the verbal rating scale (VRS) for pain. Duration of analgesia postoperative complications.


Description:

Technique for ultrasound guided infraclavicular brachial plexus block: Preliminary scan - The patient is positioned supine with the arm abducted to 90°(or resting by their side if unable to do so). - The probe is placed immediately medial to the coracoid process in the parasagittal plane. - Identify the pectoralis major and minor muscles superficially and the axillary artery and vein(s) deep to this. The vein is usually caudad relative to the artery. - The cords of the brachial plexus are seen as either hypoechoic or hyperechoic structures positioned around the axillary artery. The lateral cord is lateral (cephalad) to the artery, the medial cord medial (caudad),and the posterior cord posterior (deep). They can be difficult to visualize but are usually positioned closely to the artery. Ultrasound settings - Probe: high-frequency (>10MHz) linear broadband probe. - Settings: MB-resolution/general. - Depth: 3-6cm. - Orientation: parasagittal. - Needle: 50-100mm depending on depth of plexus. Technique - An in-plane approach is recommended, inserted from the cephalad end of the transducer. - Needle tip visualization may be challenging as the needle angle can be quite steep. - Prepare the skin with 0.5% chlorhexidine in 70% alcohol. Wait until the skin is dry. - Anaesthetize the skin with a subcutaneous injection of 1% lidocaine at the point of needle insertion. - The needle is first advanced posterolateral to the artery to deposit local anesthetic around the posterior cord, 5 o'clock position on artery. - After careful aspiration LA is injected in small aliquots, observing the spread of the LA which ideally occurs behind and up both sides of the artery forming a 'U' shape around the artery, 1-9 o'clock around the artery. - If medial (caudad) spread is not observed then reinsertion of the needle between the axillary artery and vein, adjacent to the medial cord may be required.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date October 1, 2020
Est. primary completion date April 1, 2020
Accepts healthy volunteers No
Gender All
Age group 20 Years to 65 Years
Eligibility Inclusion Criteria: - Age: 20-65 years old. - American society of anesthesiologist physical status (ASA): I-II. - Operation: forearm & hand surgeries. Exclusion Criteria: - Patients with chronic pain - Those using chronic analgesic medications - History of brachial plexus injury - Allergy to the study drugs - Hepatic or renal insufficiency or infection at the site of injection

Study Design


Intervention

Drug:
Levobupivacaine(chirocaine) plus dexmedetomidine(precedex)
evaluate the efficacy of levo-bupivacaine alone and with dexmedetomidine in Ultrasound guided infraclavicular brachial plexus block for hand and forearm surgeries

Locations

Country Name City State
Egypt Zaher Cairo

Sponsors (1)

Lead Sponsor Collaborator
Aswan University Hospital

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Onset time of sensory block in minutes After the injection of the solution, every patient was checked for the onset of sensory blockade using goose soaked with iced normal saline by the following scale (three-point scale): Grade 0= perceived as normal sensation, Grade 1 = loss of cold sensation (analgesia), Grade 2= loss of sensation of touch (anesthesia). 45 minutes
Primary onset time of motor blockade in minutes using the modified Bromage scale (Three-point scale) the modified Bromage scale (Three-point scale): Grade 0: Normal motor function, Grade 1: Decreased motor strength with the ability to move the fingers only, Grade 2: Complete motor block with an inability to move the fingers. 24 hours
Primary Duration of sensory block in hours It's the time from sensory block onset to the time of restoration of sensation at the surgical site 24 hours
Primary Duration of motor block in hours It's the time from motor block onset to the restoration of global mobility in the hand and the wrist. 24 hours
Secondary Visual analog scale (VAS) the VAS consisted of a straight, vertical 10-cm line; the bottom point represented "no pain" = (0 cm) and the top "the worst pain you ever have" = (10 cm) 24 hours
Secondary Postoperative first analgesic request time in hours was taken from the time of complete sensory block to the request to rescue analgesia when VAS > 4 cm. 24 hours
Secondary Mean blood pressure in mmHg was measured before the block (0 min) and at 5, 10, 15, 30 min then 1, 2, 3, 6, 12,18and 24 h after the block 24 hours
Secondary heart rate in beats / minute was measured before the block (0 min) and at 5, 10, 15, 30 min then 1, 2, 3, 6, 12,18and 24 h after the block. 24 hours
Secondary peripheral oxygen saturation was measured before the block (0 min) and at 5, 10, 15, 30 min then 1, 2, 3, 6, 12,18and 24 h after the block. 24 hours
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