Regional Anesthesia Morbidity Clinical Trial
Official title:
Randomized Comparative Study Between Single-injection , Intra- Cluster -Injection and Double-injection Ultrasound-guided Supraclavicular Block of Brachial Plexus
Verified date | June 2017 |
Source | Cairo University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Supraclavicular block of brachial plexus is a type of regional anesthesia sometimes employed
as an alternative to general anesthesia for surgery of the forearm. Many approaches have
been described for ultrasound-guided supraclavicular block of the brachial plexus , Double-
injection technique , single-injection and intra- cluster-injection technique. In intra-
cluster-injection technique.The comparison between the 3 techniques may allow detecting the
most beneficial one. the investigators hypothesized that intra-cluster-injection technique
will be associated with more rapid onset, longer duration and the least complications.
(because the trunks and divisions of the brachial plexus are relatively close as they travel
over the first rib, the onset and quality of anesthesia will be faster and complete) Methods
: This study will be conducted at kasr al ainy Hospital Cairo university After obtaining
ethics committee approval and written informed consent 36 patients (who will undergo surgery
for forearm)included in the study classified into three groups Gs single injection technique
,Gic intra- cluster injection technique, Gd double injection technique After block will be
done, a second investigator will examine the patient for sensory and motor block (every 10
minutes for 30 minutes) and for occurrence of complications. The patient will be ready for
surgery when the score ≥14 point. At this point the onset will be determined and so the
patient can be transferred to the operating room .
If the patient experienced anxiety, propofol infusion (80-250 ug/kg/min) can be started. If
the patient experienced pain during surgery the block considered failed and induction of
general anesthesia should be started.
After end of the surgery the second investigator will continue to assess the patient for
post operative pain every one hour for 24 hours to determine duration of the block.
Status | Enrolling by invitation |
Enrollment | 36 |
Est. completion date | September 2017 |
Est. primary completion date | September 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility |
Inclusion Criteria: 1. Age ( 18 -60 years) 2. ASA l & ASA II 3. Body mass index(20-35 Kg/m2) Exclusion Criteria: 1. Pre-existing neuropathy 2. ASA lll & ASA lV 3. Previous operation in supraclavicular fossa 4. Coagulopathy 5. Allergy to local anesthetic 6. Pregnancy 7. Inability to visualize the brachial plexus during ultrasound scanning. |
Country | Name | City | State |
---|---|---|---|
Egypt | Faculty of medicine CAIRO UNIVERISTY | Cairo |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Complications | intravascular injection , pneumothorax or horner syndrome | from injection till 24 hours postoprative | |
Other | Time of first postoperative rescue analgesic | the first time the patient ask for analgesia | from injection till 24 hours postoprative | |
Primary | onset of the block onset of anesthesia ( time in minutes from introduction of needle to appearance of 14 point score for motor and sensory block ) onset of the block | time in minutes from introduction of needle to appearance of 14 point score for motor and sensory block ) | from 0- 25 minutes after complete injectio | |
Secondary | Duration of the block | from onset to appearance of pain in surgery site | 25 minutes after injection till 6 hours post oprative |
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