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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03409068
Other study ID # 0174363/2017
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 28, 2018
Est. completion date January 18, 2019

Study information

Verified date April 2019
Source San Salvatore Hospital of L'Aquila
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

C2-C4 compartment block compared to the Costaiola block, in the control of persistent postoperative pain (somatic and neuropathic) in patients undergoing carotid thromboendarterectomy


Description:

A comparative analysis will assess the somatic pain (scores ≥4 on the NRS scale) and neurapathic pain (by the Lindblom roller and Von Frei hair tests) between group A (block group of the C2-C4 compartment ) and the control group B (block group according to Costagliola), during the 3 months after surgery.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date January 18, 2019
Est. primary completion date November 28, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- patients undergoing to carotid thromboendarterectomy

Exclusion Criteria:

- ASA status: 4

- pregnancy

- BMI > 39,99

- neurological impairment

- neck anatomical abnormalities

- status of sepsis

- coagulopathy

- neck cancer

- neck infections

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
C2-C4 compartment anesthetic block
C2-C4 compartment anesthetic block is performed by injecting levobupivacaine 0.375% 20 mL between the posterior face of the middle scalenus muscle, the anterior face of the posterior scalene muscle and the lower plane of the sternoscleidomastoid muscle.
Costagliola block
Costagliola block is performed by injected by injecting levobupivacaine 0.375% 20 mL along the anterior and the posterior border of sternocleidomastoid muscle

Locations

Country Name City State
Italy SS Filippo and Nicola Academic Hospital of Avezzano Avezzano L'Aquila

Sponsors (1)

Lead Sponsor Collaborator
San Salvatore Hospital of L'Aquila

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary somatic pain Somatic pain assessed by Numeric Pain Rating Scale for pain (the 11-point numeric scale ranges from '0' representing "no pain" to '10' representing the "worst pain imaginable" 3 mounths after surgery
Secondary Opiates request Request of opiates, assessed in mg of equianalgesic dose of morphine after 3 mouths from surgery 3 mounths after surgery
Secondary Pregabalin request Pregabalin request in mg, 3 months after surgery 3 months
Secondary Neuropathic pain Presence of neuropathic disturbances, assessed with von Frey hair test and Lindblom test 3 months
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