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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04544228
Other study ID # MS-101-2020
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 5, 2020
Est. completion date March 1, 2021

Study information

Verified date March 2021
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to Investigate the analgesic efficacy of adding ketamine compared to neostigmine to local anesthetic in Ultrasound guided Serratus anterior plane block for patients undergoing Modified Radical Mastectomy.


Description:

Breast cancer is the most common malignancy among females with incidence of 18,660 patients each year in Egypt. Modified Radical Mastectomy is considered the main surgical management for breast cancer accounting for 31% of all breast surgery cases. Ultrasound guided Serratus anterior plane block provides analgesia for breast and lateral thoracic wall surgeries by blocking nerves that are located in a compartment between the serratus anterior and the latissimus dorsi muscles ( the intercostobrachial nerve, lateral cutaneous branches of the intercostal nerves (T3-T9), long thoracic nerve and thoracodorsal nerve). A previous study demonstrated the analgesic efficacy of ketamine in patients undergoing modified pectoral nerve block in breast cancer surgery as evidenced by prolonged time to first rescue analgesia and reduced total opioid consumption. Neostigmine has been used as an additive to local anesthetics to prolong the analgesic effect. Although there is good evidence for a spinal action of neostigmine, its analgesic efficacy as an adjuvant to local anesthetic is still unclear. The aim of this study is to Investigate the analgesic efficacy of adding ketamine compared to neostigmine to local anesthetic in Ultrasound guided Serratus anterior plane block for patients undergoing Modified Radical Mastectomy.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date March 1, 2021
Est. primary completion date February 20, 2021
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - ? Female patients - Type of surgery; Modified Radical Mastectomy (MRM). - Physical status ASA II, III. - Age = 21 and = 65 Years. - Body mass index (BMI): > 20 kg/m2 and < 35 kg/m2. Exclusion Criteria: - ? Patients with Known sensitivity or contraindication to drug used in the study (local anesthetics, opioids). - History of psychological disorders and/or chronic pain. - Contraindication to regional anesthesia e.g. local sepsis, pre- existing peripheral neuropathies and coagulopathy. - Infection of the skin at the site of needle puncture area - Patient refusal. - Severe respiratory or cardiac disorders. - Advanced liver or kidney disease. - Pregnancy. - Patient with surgery duration more than two hours

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Serratus Anterior Plane Block Technique
The patient will be placed in Lateral Decubitus with a surgical side upwards with arm abduction. A linear ultrasound transducer (6-13 MHz) will be placed on the patient's midaxillary line in the transverse plane, at the level of the fifth rib, with the indicator oriented toward the operator's left. With the rib, pleural line, and overlying serratus anterior and latissimus dorsi muscles visualized, local infiltration of the skin and subcutaneous tissue will be applied by 2-3ml of lidocaine 2%. Then, using ultrasound guidance, A 38-mm 22-gauge regional block needle will be advanced in-plane at an angle of approximately 45 degrees towards the fifth rib. The expecting depth for this block is 1-4 cm. After aspiration, injection 30ml local anesthetic mixture will be injected anteriorly to the rib and deep to the serratus anterior muscle.
General anesthesia
Induction of general anaesthesia will be performed using a regimen of IV 2 µg/kg fentanyl and propofol IV 2 mg /kg. Tracheal intubation will be facilitated using 0.5 mg/kg IV of rocuronium. Anaesthesia will be maintained with inhaled sevoflurane 2-2.5% in oxygen enriched air (FiO2=0.5). Maintenance doses of rocuronium 0.1 m\kg will be provided every 30 minutes. The residual neuromuscular blockade will be reversed using neostigmine (0.05 mg/kg) and atropine (0.02 mg/kg), and extubation will be performed after complete recovery of the airway reflexes.
Drug:
bupivacaine +ketamine
30 ml bupivacaine 0.25% + 1 ml ketamine (50mg) in Serratus Anterior Plane Block.
bupivacaine + neostigmine
30 ml bupivacaine 0.25% + 1 ml neostigmine (500 µg)in Serratus Anterior Plane Block.
bupivacaine +saline
30 ml bupivacaine 0.25% + 1 ml normal saline in Serratus Anterior Plane Block.

Locations

Country Name City State
Egypt Faculty of medicine-Cairo University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

References & Publications (3)

Blanco R, Parras T, McDonnell JG, Prats-Galino A. Serratus plane block: a novel ultrasound-guided thoracic wall nerve block. Anaesthesia. 2013 Nov;68(11):1107-13. doi: 10.1111/anae.12344. Epub 2013 Aug 7. — View Citation

El Mourad MB, Amer AF. Effects of adding dexamethasone or ketamine to bupivacaine for ultrasound-guided thoracic paravertebral block in patients undergoing modified radical mastectomy: A prospective randomized controlled study. Indian J Anaesth. 2018 Apr;62(4):285-291. doi: 10.4103/ija.IJA_791_17. — View Citation

Pandey V, Mohindra BK, Sodhi GS. Comparative evaluation of different doses of intrathecal neostigmine as an adjuvant to bupivacaine for postoperative analgesia. Anesth Essays Res. 2016 Sep-Dec;10(3):538-545. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Time of first request of analgesia it will be calculated from the time of complete injection of local anesthetics till the numerical rating scale (NRS) is =3. 24 hours postoperative
Secondary The total amount of morphine consumption Rescue analgesia will be provided in the form of IV morphine 3 mg boluses if the patient indicates Numeric Pain Rating Scale = 3. The total amount of morphine given in 24 hours will be recorded for the three groups. 24 hours postoperative
Secondary Total amount of intraoperative fentanyl. Rescue analgesia of fentanyl 1 µg/kg will be given if the mean arterial blood pressure or heart rate rises above 20% of baseline levels. 2 hours
Secondary Numeric Pain Rating Scale A numerical rating scale (NRS) requires the patient to rate their pain on a defined scale. For example, 0-10 where 0 is no pain and 10 is the worst pain imaginable 24 hours
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