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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04644562
Other study ID # FMBSUREC/05072020/Abd El Badei
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 20, 2020
Est. completion date January 30, 2021

Study information

Verified date November 2020
Source Beni-Suef University
Contact doaa rashwan, md
Phone 00201011270763
Email doaa_rashwan@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the investigatots hypothesized that by injection a larger volume and higher concentration of local anesthetic in lumbar erector spinae plane block could result in successful anesthesia in patient undergoing lower limb vascular surgery. ultrasound-guided lumbar erector spinae plane block in patient undergoing lower limb vascular surgery with higher concentration of local anesthetic to asses it is efficacy as a sole anesthetic technique, it is safety and efficacy in maintaining intraoperative hemodynamics, intra and postoperative pain control .


Description:

The patients will placed in lateral position. After aseptic preparation of the skin and probe, a high-frequency linear ultrasound transducer will move about 3 cm laterally on the parasagittal plane to visualize the transverse process of the (L2) vertebra. An 18-guage tuohy needle will be approached in-plane lateral to medial. When the needle initially touched the transverse process of L3 vertebrae, the needle will be gently withdrawn and hydrodissection of the plane achieved, lifting the erector spinae muscle. A 20-guage catheter will be introduced through the needle and total length inserted will be 3 cm more than the tip of needle (. 25 mL of 0.5% bupivacaine ( in increments slowly after negative aspiration will be injected in the interfascial plane observing the anesthetic spread. Sensory and motor block will be evaluated and surgery will begin only after adequate block , if failed, general anesthesia will induced by injecting 1.5-2 mg/kg propofol, 2 μg/kg fentanyl & 0.5 mg/kg atracurium. The patients will be ventilated via face mask with 100 % oxygen at a rate of 4 L/min and isoflurane 1.2 %. After 3 minutes, the patients will be intubated using appropriate sized cuffed oral tube lubricated with lidocaine jelly 2 % . Maintenance of anesthesia will done using isoflurane 1.2 % in 100 % O2. Muscle relaxation will be continued by atracurium 0.1 mg/kg every 20 min. All patients will be mechanically ventilated to maintain end-tidal carbon dioxide between 35-40 mmHg. For 5 minutes, no surgical interventions will be allowed in the subjects to assess target blood pressure.


Recruitment information / eligibility

Status Recruiting
Enrollment 5
Est. completion date January 30, 2021
Est. primary completion date January 30, 2021
Accepts healthy volunteers No
Gender All
Age group 40 Years to 65 Years
Eligibility Inclusion Criteria: - ASA II and III male and female patients undergoing lower limb vascular surgery Exclusion Criteria: - Contraindications for regional blocks (eg. Patient refusal Infection at the injection site, coagulopathy) - allergic reaction to drugs. - opium addiction, any drug or substance abuse and chronic treatment with opium, non-steroidal anti-inflammatory drugs

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Erector Spinae plane block
Ultrasound-guided lumbar Erector Spinae plane block in patients undergoing Lower Limb vascular Surgery

Locations

Country Name City State
Egypt Benisuef univercity Bani Suwayf, Benisuef

Sponsors (1)

Lead Sponsor Collaborator
Beni-Suef University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary motor block block level motor power baseline, pre-intervention/procedure/surgery
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