AzTrials
AzTrials

Breast CancerNCT04606147

Effectiveness of Ultrasound Guided Erector Spinae Plane Block Against Ultrasound Guided Serratus Anterior Block in Modified Radical Mastectomy

A study testing Serratus Anterior Plane Block and Erector spinae plane block in people with Breast Cancer and Postoperative Pain, run by National Cancer Institute, Egypt at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The aim of this study is to compare and evaluate the safety and analgesic efficacy of ultrasound guided ESP block and ultrasound guided serratus anterior plane block in patients undergoing modified radical mastectomy. Read more about this study

Who is it for?
Ages 18 to 65 years, women onlyHealthy volunteers can take part
Conditions the study is for
Breast Cancer, Postoperative Pain
What is being tested?
Serratus Anterior Plane Block and Erector spinae plane block
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteEgypt
Study dates
10 Jan 2020to 20 May 2020
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • Women only
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Female patients
  • Type of surgery; Modified Radical Mastectomy MRM
  • Physical status ASA II, III.
  • Age ≥ 18 and ≤ 65 Years.
  • Body mass index (BMI): ≥ 20 kg/m2 and ≤ 35 kg/m2.

Who cannot join

  • Age: ≤18 years or ≥65 years
  • BMI: ≤20 kg/m2 or ≥ 35 kg/m2
  • Known sensitivity or contraindication to drugs used in the study (local anaesthetics, opioids).
  • History of psychological disorders and/or chronic pain syndrome.
  • Contraindication to regional anaesthesia e.g. local sepsis, pre-existing peripheral neuropathies and coagulopathy.
  • Patient refusal.
Show all 11Show fewer
  • Severe respiratory or cardiac disorders.
  • Advanced liver or kidney disease.
  • Pregnancy.
  • Physical status ASA IV
  • Male patients.

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • National Cancer Institute - Cairo University

    Cairo

Other trials in Egypt

About this study

Official title: Comparison of Effectiveness of Ultrasound Guided Erector Spinae Plane Block With Ultrasound Guided Serratus Anterior Block in Modified Radical Mastectomy, Randomized Single Blinded Comparative Study.

The aim of this study is to compare and evaluate the safety and analgesic efficacy of ultrasound guided ESP block and ultrasound guided serratus anterior plane block in patients undergoing modified radical mastectomy.

Read the detailed description

Methodology:

This Randomised Comparative Single Blinded Study was conducted at National Cancer Institute Cairo University after approval by the institutional review board, scientific committee of Anesthesia department Kasr Alainy Cairo University (02/10/2019 Code: N - 65\2019 ms) and Ethical committee at Kasr Alainy Cairo University (1\ 12 \2019 code: MS-268-2019)

Type of consent of study participants: Written and verbal

Study Methods:

Population of study: 60 Female patients ASA II, III scheduled for modified radical mastectomy under general anaesthesia.

Methodology in details:

Randomization:

The patients were randomly assigned into two equal comparable groups using computer- generated random numbers in opaque closed envelopes, each of which included 30 patients.

Randomization was done by a statistician and group of the patient was revealed only when the included patient is transferred to the preanesthetic room.

Study Protocol:

Patient assessment; History, physical exam, laboratory and radiological investigations at preoperative assessment clinic National Cancer Institute Cairo University.

Preoperative assessment at night of surgery. The patients were instructed how to report pain by means of Numeric Pain Rating Scale, in which 0 = no pain and 10 =worst possible pain. Informed consent was obtained.

Preoperative fasting; minimum of 6 hours for food and minimum of 2 hours for water and clear fluids. 20G IV cannula was inserted. All patients premedicated with IV midazolam 0.01-0.02mg\kg 30 minutes preoperatively. Both blocks were done preoperative with the patients at lateral position.

After allocation of the patient to a study group patients of group 1 received serratus anterior plane block and patients of group 2 received erector spinae plane block.

Serratus Anterior Plane Block Technique;

The block is performed with full aseptic precautions. Lateral Decubitus with arm abduction is preferred. Ultrasound probe should 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, the skin and subcutaneous tissue can be topicalized with 3 ml of lidocaine 1%. Then, using ultrasound guidance, A 38-mm 22-gauge regional block needle is advanced in-plane at an angle of approximately 45 degrees towards the fifth rib.

Correct location of the needle tip in the fascial plane deep to serratus anterior muscle will be confirmed by injecting 0.5-1 ml normal saline and seeing hydrodissection of fascial plane between SAM and 5th rib. After aspiration to avoid intravascular injection 30 ml of levobupivacaine 0.25% is injected anteriorly to the rib and deep to the serratus anterior muscle. The entirety of the needle should be visualized at all times throughout the procedure, and care should be taken to avoid any vessels while traversing the soft tissue.6-13-MHz, linear transducer set for small parts and a depth of 1-4 cm was used for this block.

Erector spinae plane block Technique; The block is performed with full aseptic precautions. Block level at T5. Ultrasound probe placed on the back in a transverse orientation to identify the tip of the T5 transverse process; these are recognizable as flat, squared-off acoustic shadows with only a very faint image of the pleura visible. If the transducer is too lateral, the ribs will be visualized instead; these are recognizable as rounded acoustic shadows with an intervening hyperechoic pleural line. The tip of the transverse process centered on the ultrasound screen and the probe will then be rotated into a longitudinal orientation to produce a parasagittal view, in which the following layers will be visible superficial to the acoustic shadows of the transverse processes: skin and subcutaneous tissue, trapezius, erector spinae muscle and T5 transverse process. A skin wheal using 3ml of 1% lidocaine is made , then echogenic block needle will be inserted in- plane to the ultrasound beam in a cranial-to-caudal direction until contact is made with the T5 transverse process. Correct location of the needle tip in the fascial plane deep to erector spinae muscle will be confirmed by injecting 0.5-1 ml normal saline and seeing the fluid lifting the erector spinae muscle off the transverse process without distending the muscle. After aspiration to avoid intravascular injection 30 ml levobupivacaine 0.25% was injected and separation was seen. 6-13-MHz, linear transducer set for small parts and a depth of 4-6 cm was used (59-62).

In both blocks Fujifilm Sonosite M-Turbo Ultrasound system was used.

After performing blocks lung ultrasound was performed to exclude pneumothorax, chest was divided to 6 quadrants with the patient semi sitting:

Anterior upper and lower quadrants Lateral upper and lower quadrants Posterior upper and lower quadrants All quadrants scanned especially upper quadrants was scanned looking for signs of pneumothorax such as absence of lung sliding, presence of B lines, barcode or stratosphere sign and lung-point sign. 6-13-MHz, linear transducer set for small parts and a depth of 4-6 cm was used.

Lung us was done after performing block and post operative at PACU

Patients transferred to the post-anaesthesia care unit (PACU) where the Numeric Pain Rating Scale score, MAP and heart rate were noted immediately on arrival, where they will be observed for 2 hours then discharged to the ward. Lung ultrasound was done once again at PACU looking for signs of pneumothorax. Rescue analgesia was provided in the form of IV morphine 3 mg boluses when the patient indicates Numeric Pain Rating Scale score ≥ 4. The total amount of morphine given in 24 hours was recorded for the two groups. A maximum dose of 0.5 mg/kg/24hours of morphine was allowed.

After that Modified Radical Mastectomy is performed under GA.

After the patients were transferred to their respective ward, Multimodal analgesia was provided as the following:

IV paracetamol 500 mg \6 hours IV ketorolac 30mg\8 hours.

Sample size:

The investigators plan was to study continuous response variable (post operative morphine consumption in the1 st 24 hours) from independent control and experimental with 1 control per 1 experimental subject. The experimental group is Erector spinae plane block (ESPB) versus control group Serratus Anterior Plane Block (SAP). In a previous randomized controlled trial by Gupta et al (2017), comparing Analgesic efficacy of ultrasound-guided paravertebral block with serratus anterior plane block for modified radical mastectomy mean postoperative morphine consumptions in (SAP) group was found to be 9.2 ± 2.1 mg. In another study by Singh et al (2019), which compares analgesic efficacy of Erector spinae plane block (ESPB) with opioid based anaesthesia mean postoperative morphine consumptions in (ESPB) was 1.9 ± 2.01 mg. If the true difference in the control and experimental means is7.8, A sample size of 14 experimental subjects and 14 control subjects was needed to be able to reject the null hypothesis that the experimental and control groups are equal with probability(power) of 0.9. Type 1 error probability associated with this test of this null hypothesis is 0.01. To ensure normal distribution of response variables 30 patients per group were recruited.

Statistical analysis:

SPSS version 23.0 was used in data analysis. Mean and standard deviation described quantitative data with median and range when appropriate. Quantitative variables were tested for normality to select appropriate statistical tests. Comparison of means (or medians) of two independent groups was done using t test (parametric or non- parametric). To show the effect of time on vitals, parametric repeated measures ANOVA (or non-parametric Friedman tests) were used to show changes overtime both intra and post-operative. Post-hoc test were used for pairwise comparisons and were Bonferroni adjusted. Chi-square and Fisher Exact were used for testing proportion independence. P value was always two tailed and set significant at 0.05 level.

Sources of funding: National Cancer Institute Cairo University No conflict of interest.

Being tested
Serratus Anterior Plane Block, Erector spinae plane block
Keywords
Modified Radical Mastectomy MRM, ESPB ,SAPB , Regional anesthesia and postoperative analgesia.
Medical subject headings
Breast Neoplasms, Pain, Postoperative

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Serratus Anterior Plane BlockProcedure or surgery

    The block is performed with full aseptic precautions.in lateral position \&arm abduction. US probe placed on the patient's midaxillary line in the transverse plane, at the level of the fifth rib.With the rib, pleural line, and overlying serratus anterior and latissimus dorsi muscles visualized, the skin and subcutaneous tissue can be topicalized. Then, using ultrasound guidance, A regional block needle is advanced in-plane at an angle of approximately 45 degrees towards the fifth rib.Correct location of the needle tip in the fascial plane deep to serratus anterior muscle will be confirmed by injecting 0.5-1 ml normal saline and seeing hydrodissection of fascial plane between SAM and 5th rib. After aspiration to avoid intravascular injection 30 ml of levobupivacaine 0.25% is injected anteriorly to the rib and deep to the serratus anterior muscle. The entirety of the needle should be visualized at all times throughout the procedure.

  • Erector spinae plane blockProcedure or surgery

    The block is performed with full aseptic precautions at T5 level. T5 transverse process is identified by us as flat, squared-off acoustic shadows with only a very faint image of the pleura.In longitudinal us view following layers will be visible superficial to transverse processes: skin and subcutaneous tissue, trapezius, erector spinae muscle.Skin is topicalised , then echogenic block needle inserted in- plane to the ultrasound beam in a cranial-to-caudal direction until contact is made with the T5 transverse process. After aspiration to avoid intravascular injection 30 ml levobupivacaine 0.25% was injected and separation was seen. 6-13-MHz, linear transducer set for small parts and a depth of 4-6 cm was used

Study groups in NCT04606147
Study groupRoleWhat they receive
Group 1 ((Serratus Anterior Plane Block SAPB)) N=3oExperimentalPatients received Ultrasound guided Serratus Anterior Plane Block preoperative with injection of 30 ml levobupivacaine 0.25%. Then patients were transferred to the operating room.
Receives: Procedure: Serratus Anterior Plane Block
Group 2 ((Erector Spinae Plane Block ESPB)) N=3oExperimentalPatients received Ultrasound guided erector spinae plane block with injection of 30 ml levobupivacaine 0.25%. Then patients were transferred to the operating room.
Receives: Procedure: Erector spinae plane block

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Total amount of postoperative morphine consumption in 24 hours. (mg)

    Total amount of postoperative morphine consumption in 24 hours. (mg)

    Measured: 24 hours

Secondary outcomes (8)
  1. Total amount of intraoperative fentanyl consumption (mcg)

    Total amount of intraoperative fentanyl consumption (mcg)

    Measured: duration of surgery

  2. Change in heart rate intraoperatively

    Introperative measurement of HR at 30 minutes interval in comparison to baseline reading.

    Measured: duration of surgery

  3. The degree of postoperative sedation according to Ramsay scores.

    Post operative sedation according to Ramsay scores at 0,2,4,8,12,16,20,24 hours:

    (1 = anxious or restless or both; 2 = cooperative, orientated, and tranquil; 3= responding to commands; 4 = brisk response to stimulus; 5 = sluggish response to stimulus; and 6 = no response to stimulus). A Ramsay score of 5 or 6 considered excessively high sedation levels; a Ramsay score of 2 to 4 considered adequate sedation levels needing observation; a Ramsay score of 1 considered inadequate or insufficient sedation Levels.

    Measured: 24 hours

  4. Time to first rescue analgesia (hours)

    duration of analgesic effect until the time of 1st rescue analgesia

    Measured: postoperative

  5. Numeric Pain Rating Scale score, both at rest and during movement

    Numeric Pain Rating Scale score, both at rest and during movement at PACU, and every 4 hours until 24 hours postoperatively.The patients were instructed how to report pain by means of Numeric Pain Rating Scale, in which 0 = no pain and 10 =worst possible pain.

    Measured: 24 hours

  6. Block related complications

    Complications related to blocks such as local anaesthetic systemic toxicity, pneumothorax and arterial puncture.

    Measured: 24 hours

  7. Patient satisfaction

    the patients will be classified in this group to: satisfied or not.

    Measured: 24 hours

  8. Change in mean arterial blood pressure intraoperatively

    ntroperative measurement of MAP at 30 minutes interval in comparison to baseline reading.

    Measured: duration of surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Oct 2020
  2. Study start10 Jan 2020
  3. Primary completion20 May 2020
  4. Study completion20 May 2020

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Investigator
Enrolment
60 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04606147
Sponsor's protocol ID
MS-268-2019
Status last verified
Oct 2020
First submitted
21 Oct 2020
Last updated
28 Oct 2020
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Garg R, Bhan S, Vig S. Newer regional analgesia interventions (fascial plane blocks) for breast surgeries: Review of literature. Indian J Anaesth. 2018 Apr;62(4):254-262. doi: 10.4103/ija.IJA_46_18.

    PubMed 29720750
  • De Cassai A, Bonvicini D, Correale C, Sandei L, Tulgar S, Tonetti T. Erector spinae plane block: a systematic qualitative review. Minerva Anestesiol. 2019 Mar;85(3):308-319. doi: 10.23736/S0375-9393.18.13341-4. Epub 2019 Jan 4.

    PubMed 30621377
  • Blanco R. The 'pecs block': a novel technique for providing analgesia after breast surgery. Anaesthesia. 2011 Sep;66(9):847-8. doi: 10.1111/j.1365-2044.2011.06838.x. No abstract available.

    PubMed 21831090
  • Smith WC, Bourne D, Squair J, Phillips DO, Chambers WA. A retrospective cohort study of post mastectomy pain syndrome. Pain. 1999 Oct;83(1):91-5. doi: 10.1016/s0304-3959(99)00076-7.

    PubMed 10506676
  • Forero M, Adhikary SD, Lopez H, Tsui C, Chin KJ. The Erector Spinae Plane Block: A Novel Analgesic Technique in Thoracic Neuropathic Pain. Reg Anesth Pain Med. 2016 Sep-Oct;41(5):621-7. doi: 10.1097/AAP.0000000000000451.

    PubMed 27501016
  • 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.

    PubMed 23923989
  • Gupta K, Srikanth K, Girdhar KK, Chan V. Analgesic efficacy of ultrasound-guided paravertebral block versus serratus plane block for modified radical mastectomy: A randomised, controlled trial. Indian J Anaesth. 2017 May;61(5):381-386. doi: 10.4103/ija.IJA_62_17.

    PubMed 28584346
  • Singh S, Kumar G, Akhileshwar. Ultrasound-guided erector spinae plane block for postoperative analgesia in modified radical mastectomy: A randomised control study. Indian J Anaesth. 2019 Mar;63(3):200-204. doi: 10.4103/ija.IJA_758_18.

    PubMed 30988534

Questions about this trial

What is this clinical trial studying?

A study testing Serratus Anterior Plane Block and Erector spinae plane block in people with Breast Cancer and Postoperative Pain, run by National Cancer Institute, Egypt at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 28 Oct 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Total amount of postoperative morphine consumption in 24 hours. (mg) (time frame: 24 hours). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04606147, which also lists 8 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Oct 2020.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in