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CompletedNCT04841564Updated Aug 27, 2024

Open Versus Ultrasound Approach for Serratus Anterior Block

An interventional study of ultrasound approach of serratus anterior block and open approach of serratus anterior block in Analgesia, sponsored by Mansoura University. Completed at 1 site in Egypt. Open to female participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2024-08-27.

Sponsored by Mansoura University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
46
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
Female
01

Study summary

Ultrasound-guided Serratus anterior plane (SAP) block is an interventional technique that recently gained popularity in the context of postoperative analgesia after breast surgery. Some limitations may be encountered during the use of ultrasound, such as obesity, tumor invasion of the surrounding muscles, which may lead to poor ultrasound image quality. The investigators hypothesized that an open approach to serratus anterior block by infiltration of local anesthetic between serratus anterior muscle and ribs after tumor excision during surgery would be non-inferior to ultrasound-guided approach where the primary endpoint of this prospective randomized blind controlled study will be the total dose of morphine consumed in the 1st postoperative 24 h. The patients will be randomly allocated to an open approach group and ultrasound approach group to serratus anterior block using computer-generated random numbers and sealed opaque envelops. For any statistical tests used results will be considered as statistically significant if P-value ≤0.05.

Read the detailed description

Modified radical mastectomy (MRM) is one of the most common surgeries performed, and one that may be associated with significant acute postoperative pain in breast surgery. Acute postoperative pain is an independent risk factor in the development of chronic post-mastectomy pain.

Various regional anesthetic procedures have been tried to provide better acute pain control and, consequently, less chronic pain. They can reduce perioperative opiates requirement and thereby decreasing their possible side effects. These regional procedures include local wound infiltration, thoracic epidural, and thoracic paravertebral block (PVB). pectoral nerves block type-1 (PECSI), pectoral nerves block type-2 (PECS II), and serratus plane block.

Ultrasound-guided Serratus anterior plane (SAP) block is an interventional technique that recently gained popularity in the context of breast surgery. SAP block resulted in better hemodynamic stability, early ambulation, and reduced duration of hospitalization as well as hospital costs in postoperative breast patients.

Some limitations may be encountered during the use of ultrasound, such as obesity, tumor invasion of the surrounding muscles, which may lead to poor ultrasound image quality. Also, ultrasound use depends on equipment quality and investigator experience.

The investigators hypothesized that an open approach to serratus anterior block by infiltration of local anesthetic between serratus anterior muscle and ribs after tumor excision during surgery would be non-inferior to ultrasound-guided approach in providing analgesia to female patients undergoing modified radical mastectomy. The primary endpoint will be the total dose of morphine consumed in the 1st postoperative 24 h. secondary outcomes will be the time of the first analgesic request (duration of the pain-free periods after surgery in the1st postoperative 24 hours), postoperative visual analog score (VAS), postoperative modified Ramsay sedation score, and PONV (post-operative nausea and vomiting).

02

Conditions studied

  • Analgesia

Keywords

  • serratus anterior block
  • ultrasound
  • open
  • mastectomy
03

In context

Lead sponsor

Mansoura University is the lead sponsor of 1,077 studies on the registry; 183 are open to participants now.

Of its 9 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • American Society of Anesthesiologists (ASA) physical status scores of I and II
  • Elective unilateral breast surgery (modified radical mastectomy)

Exclusion criteria

Exclusion Criteria:

  • Patient refusal to participate in the study.
  • Allergy to any medications used in the study.
  • Patients with coagulopathy
  • patients with psychiatric disorders.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
46 participants (actual)

Study arms

  • Active comparator
    ultrasound group

    serratus anterior plane block will be done through ultrasound guidance

    Procedure: ultrasound approach of serratus anterior block

  • Experimental
    Open group

    serratus anterior plane block will be done after mastectomy through the open wound

    Procedure: open approach of serratus anterior block

Interventions

  • Procedureultrasound approach of serratus anterior block

    After induction of general anesthesia, the ultrasound probe will be placed longitudinally oblique just below the mid-clavicle. After identifying the second rib, the probe will be moved caudally and laterally (obliquely), towards the mid-axillary line to identify the 3rd, 4th and 5th ribs.. The fascial plane between the serratus anterior muscle and latissimus dorsi muscle will be identified over the 4th rib in the mid-axillary region. The block will be performed with a needle (22-G, 50-mm) introduced in-plane to enter deep to the serratus anterior muscle, and 30 ml 0.25 bupivacaine will be injected.

    Also known as: ultrasound approach

  • Procedureopen approach of serratus anterior block

    After resection of the breast and identification of the serratus anterior muscle, the surgeon will be asked to palpate the ribs below the clavicle and localize the fourth rib. A 22-G, 50-mm needle will be introduced deep to the serratus anterior muscle contacting the rib, and 30 ml 0.25 bupivacaine will be injected.

    Also known as: open approach

06

What researchers measure

Primary outcomes

  1. Morphine consumption given as a rescue analgesia

    The amount of morphinel consumption in milligrams given as a rescue analgesia to patients when the vas score is more than 3

    Time frame: Up to 24 hours after the procedure

Secondary outcomes

  1. The period for the first analgesic required

    duration of analgesia in minutes

    Time frame: Up to 24 hours after the procedure

  2. Mean arterial blood pressure

    Mean arterial blood pressure in mmHg will be recorded at baseline before surgical incision and postoperatively at 1, 4, 8, 12, 24 hours

    Time frame: Up to 24 hours after the procedure

  3. visual analogue score (VAS) at rest

    pain intensity will be assessed at rest with the 10 point visual analogue score (VAS) where 0 =no pain and 10 = the worst imaginable pain and the time points of measurements will be at 0, 1, 4, 8, 12 and 24 hours post-operatively.

    Time frame: Up to 24 hours after the procedure

  4. postoperative complications

    Any postoperative events like nausea, vomiting, respiratory depression( respiratory rate less than 12), urine retention, pruritis, local anesthetic toxicity and pneumothorax will be recorded.

    Time frame: Up to 24 hours after the procedure

  5. Heart rate

    Heart rate in beats per minute will be recorded at baseline before surgical incision and postoperatively at 1, 4, 8, 12, 24 hours

    Time frame: Up to 24 hours after the procedure

  6. visual analogue score (VAS) at shoulder movement

    pain intensity will be assessed at shoulder movement with the 10 point visual analogue score (VAS) where 0 =no pain and 10 = the worst imaginable pain and the time points of measurements will be at 0, 1, 4, 8, 12 and 24 hours post-operatively.

    Time frame: Up to 24 hours after the procedure

07

Study locations

1 site
  • Department of Anesthesia, Mansoura University Hospitals
    Mansoura, Dakahlia 35511, Egypt
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 27, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04841564
Lead sponsor
Mansoura University
Responsible party
Mahmoud Mohammed Alseoudy (Lecturer of anesthesia, ICU & pain management; Faculty of Medicine, Mansoura University) — Principal investigator
First posted
Apr 12, 2021
Start date
Apr 10, 2021
Primary completion
Jun 15, 2024
Completion
Jul 20, 2024
Last update
Aug 27, 2024

Study contacts

Mahmoud M Alseoudy, MD
principal investigator · mansoura university, faculty of medicine

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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