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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06208774
Other study ID # N-403-2023
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 20, 2023
Est. completion date May 30, 2024

Study information

Verified date January 2024
Source Cairo University
Contact Nagy malak, MD
Phone 01552480258
Email nagymalak1234@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to compare PENG block and LV-ISBP block in the incidence of phrenic nerve block, duration of postoperative analgesia, time to first analgesic request (VAS > 30 mm), pain scores, and side effects.


Description:

This randomized, controlled, double-blinded trial will be conducted in a Cairo University hospital.On arrival of the patients in the regional anesthesia room, they will be secured with a 20-gauge intravenous cannula. Monitoring will include ECG, non-invasive arterial blood pressure, and pulse oximetry (SpO2). Before receiving the blocks, patients will be randomly assigned to one of the two study groups for diaphragmatic movement assessment: The diaphragmatic excursion will be measured in the supine position before the block and after surgery by a blinded operator. A curvilinear ultrasound probe (5-7 MHz) will be placed at the subcostal area in the anterior axillary line, below the costal margin of the eighth and ninth ribs. The probe will be directed medially, cephalad, and dorsally to make the ultrasound beam reach the posterior third of the diaphragm perpendicularly. The probe will then be scanned along the long axis of the intercostal spaces, using the liver as the acoustic window on the right side and the spleen as the acoustic window on the left side. The M-mode sampling line will be positioned perpendicularly to the diaphragm, and the diaphragmatic excursions could be measured during quiet and deep breathing. The distance between the resting expiratory position and the maximum deep inspiration position will be measured. The measurement will be repeated three times, and the average value will be taken. After measurement of diaphragmatic excursion, patients will receive either a PENG block or an LV-ISBP block before induction of general anesthesia, and to achieve double blinding, patients will receive the block by consultant anesthesiologists who have experience in regional anesthesia. Another doctor not involved in the block procedure will evaluate the patient intraoperatively and postoperatively. PENG block group (n = 40): this group will receive an ultrasound-guided pericapsular nerve group block for the shoulder with a total volume of 20 mL and 0.5% bupivacaine. LV-ISBP block group (n = 40): this group will receive ultrasound-guided low-volume interscalene brachial plexus block with a total volume of 5 mL and 0.5% bupivacaine. Technique of PENG Block: The technique of ultrasound-guided PENG block will be performed with the patient's arm placed in external rotation and abducted at 45 degrees. A linear ultrasound probe (4-12 MHz) will be placed longitudinally between the coracoid and the humeral head, visualizing the deltoid muscle and subscapularis tendon. A 22-gauge needle will be advanced in-plane, into the fascial plane between the deltoid muscle and subscapularis tendon. The location of the needle tip will be confirmed by hydrodissection of inter-fascial planes with 3 ml of normal saline. After negative aspiration, a total of 20 mL of bupivacaine 0.5% will be injected in the fascial plane incrementally, aspirating every 5 ml. Technique of the LV-ISBP block: The technique of ultrasound-guided LV-ISBP will be performed with the patient in a semi-sitting position with the head tilted to the opposite side of the injection site. A linear ultrasound probe (4-12 MHz) will be placed parallel to the clavicle in the supraclavicular fossa, and the subclavian artery will be seen beating above the first rib. Then the probe will be moved cranially to identify the transverse process of the C7 vertebra at the level of the brachial plexus roots between the scalenus anterior and medius muscles. A volume of 2 mL of 2% lignocaine will be infiltrated subcutaneously before the block. The needle will be inserted in a plane approach from lateral to medial to scalenus medius and C5-C6 brachial plexus roots. The location of the needle tip will be confirmed by hydrodissection with 1 ml of normal saline. After negative aspiration, a total of 5 mL of bupivacaine 0.5% will be injected incrementally, aspirating every 2.5 mL. To ensure blind assessment, a dressing will be placed to cover a standard area that will cover the puncture sites regardless of which block is performed. In the operating room, induction of general anesthesia will be induced after adequate preoxygenation using 1 µg/kg fentanyl, 2 mg/kg propofol, and 0.5 mg/kg atracurium, in addition to 8mg IV dexamethasone for the prevention of postoperative nausea and vomiting. Endotracheal intubation will be established. Anesthesia will be maintained by 1.2% MAC of isoflurane with oxygen (50%) in the air, and 0.1 mg/kg of atracurium will be administered every 20 minutes as maintenance anesthetic drugs. Volume-controlled ventilation will be maintained, and the respiratory rate will be adapted to maintain ET CO2 between 35 and 40 mmHg. Monitoring through ECG, NIBP, pulse oximetry, and capnography (ETCO2) continued throughout the surgeries. Each portal skin of the arthroscopy will be infiltrated by the surgeon with approximately 4 mL of 0.25% bupivacaine. Intraoperative inadequate analgesia, indicated by an increase in HR or mean arterial blood pressure (MAP) more than 20% above preinduction baseline values, will be managed using incremental 50-microgram doses of fentanyl. Intraoperative fentanyl consumption will be calculated. All patients will receive ketorolac 30mg IV and paracetamol 1 mg for postoperative analgesia. At the end of surgery, muscle relaxants will be reversed using neostigmine 0.05 mg/kg and atropine 0.02 mg/kg. Awake extubation will be established after adequate reversal of the neuromuscular block. Patients will be transported to the post-anesthesia care unit (PACU) for one hour before being shifted to the ward. In the PACU, after the patient regains full consciousness, the diaphragmatic movement will be reassessed in the exact same manner as preoperatively. Phrenic nerve block is defined as failure of the diaphragm to achieve 25% of the pre-block excursion value. Postoperative pain will be assessed using VAS (where 0 corresponds to no pain and 100 mm to the worst pain) at 2, 4, 6, 12, 18, and 24 hours postoperatively. Postoperatively, in the ward, all patients will receive 1 g paracetamol every 6 h and 30 mg ketorolac every 12 h. If the VAS score is > 30 mm, IV morphine increments (2 mg) will be given to maintain VAS ≤ 30 mm with a maximum total 24-hour morphine consumption of 10 mg, and total morphine consumption will be recorded.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date May 30, 2024
Est. primary completion date May 30, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Patients scheduled for shoulder arthroscopy - American Society of Anesthesiologists (ASA) status I and II - Ages between 18 and 60 years. Exclusion Criteria: - Coagulopathy - Infection at the injection site. - Allergy to local anesthetics - Severe cardiopulmonary disease (=ASA III) - Diabetic or other neuropathies - Motor disorders - Patients receiving opioids for chronic analgesic therapy. - Inability to comprehend visual analogue scale (VAS).

Study Design


Intervention

Procedure:
Ultrasound-guided PENG or ISBP block
The diaphragmatic excursion will be measured in the supine position before the block and after surgery. A curvilinear US probe (5-7 MHz) will be placed at the subcostal area in the anterior axillary line, below the costal margin of the eighth and ninth ribs. The probe will be directed medially, cephalad, and dorsally to make the US beam reach the posterior third of the diaphragm perpendicularly. The probe will then be scanned along the long axis of the intercostal spaces, using the liver as the acoustic window on the right side and the spleen as on the left side. M-mode sampling line will be positioned perpendicularly to the diaphragm, and the diaphragmatic excursions could be measured during quiet and deep breathing.The measurement will be repeated three times, and the average value will be taken. After measurement of diaphragmatic excursion, patients will receive either a PENG block or an LV-ISBP block before induction of general anesthesia.

Locations

Country Name City State
Egypt Cairo university Hospitals. kasralainy Cairo Governorate

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of phrenic nerve block Incidence of phrenic nerve block 24 hours
Secondary First analgesic request Time to first analgesic request (Visual analogue pain> 40 mm) 24 hours postoperative
Secondary Visual analogue pain score Visual analogue pain score for pain assessment (from 0 the Best to 100 the worst) at 2, 4, 6, 12, 18, and 24 hours postoperatively 24 hours postoperatively.
Secondary Total morphine requirements Total morphine requirements 24 hours postoperatively. 24 hours
Secondary Type and time of surgery Type and time of surgery up to 4 hours
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