Magnesium Sulfate With Standard Combined Costoclavicular-Suprascapular Block for Pain Relief After Shoulder Arthroscopy.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-50
SponsorAssiut University

About this trial

This study aims to evaluate whether adding magnesium sulfate to a combined costoclavicular and suprascapular nerve block improves postoperative pain control in patients undergoing shoulder arthroscopy. The study will compare pain management outcomes between patients receiving the nerve block with magnesium sulfate and those receiving the nerve block without magnesium sulfate. The main outcome will be the time to first rescue analgesia after surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age between 18-50 years

American Society of Anesthesiologists (ASA) physical status I-II.

Scheduled for elective outpatient shoulder arthroscopy.

Ability to understand the study protocol and use the NRS scale.

Disqualifiers

Refusal to participate.

Known allergy or hypersensitivity to local anesthetics or magnesium sulphate.

Coagulopathy or anticoagulant therapy contraindicating regional anesthesia.

Local infection at the block site.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Bupivacaine

    Drug

    "Bupivacaine 0.5% will be used as the local anesthetic for ultrasound-guided costoclavicular and suprascapular nerve blocks. A total of 25 mg (5 mL) will be administered for the costoclavicular nerve block and 50 mg (10 mL) for the suprascapular nerve block, for a total dose of 75 mg per participant."

  • Magnesium sulfate (MgSO4)

    Drug

    "Magnesium sulfate 150 mg (1.5 mL) will be used as an adjuvant to bupivacaine in each ultrasound-guided nerve block. A total of 300 mg (3 mL) of magnesium sulfate will be administered per participant, with 150 mg added to the costoclavicular nerve block and 150 mg added to the suprascapular nerve block."

  • Normal Saline (NS)

    Drug

    "Normal saline (0.9% sodium chloride) will be used as the control adjuvant, with 1.5 mL added to the local anesthetic solution for the costoclavicular nerve block and 1.5 mL added to the local anesthetic solution for the suprascapular nerve block, for a total volume of 3 mL per participant."

  • Costoclavicular Nerve Block

    Procedure/Surgery

    "A single-shot ultrasound-guided costoclavicular nerve block will be performed using 5 mL of 0.5% bupivacaine (25 mg), with either 1.5 mL of magnesium sulfate (150 mg) or 1.5 mL of 0.9% normal saline, according to the assigned study group."

  • suprascapular nerve block

    Procedure/Surgery

    "A single-shot ultrasound-guided suprascapular nerve block will be performed using 10 mL of 0.5% bupivacaine (50 mg), with either 1.5 mL of magnesium sulfate (150 mg) or 1.5 mL of 0.9% normal saline, according to the assigned study group."

Treatment groups

84 Participants
are divided into 3 treatment groups
Group A: Costoclavicular-Suprascapular Block with Normal SalineExperimental treatment 4 interventions
Group B: Costoclavicular-Suprascapular Block with regional Magnesium SulfateExperimental treatment 4 interventions
Group C: Costoclavicular-Suprascapular Block with Intravenous Magnesium SulfateExperimental treatment 5 interventions

Trial outcomes

Primary outcomes

1

Time to first rescue analgesia after discharge from PACU.

Time to first rescue analgesia will be measured from the time of discharge from the Post-Anesthesia Care Unit (PACU) until the first administration of rescue analgesic medication for 24 hour due to postoperative pain. Numeric Rating Scale (NRS): Pain intensity was assessed using the 11-point Numeric Rating Scale (NRS), in which 0 = no pain and 10 = the worst pain imaginable.

Time frame
From discharge from PACU until 24 hours postoperatively.

Secondary outcomes

1

Postoperative Pain Score Using the Numeric Rating Scale

Postoperative pain intensity will be assessed from the end of surgery for 24 hours postoperatively using the Numeric Rating Scale (NRS), ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst pain imaginable. Higher scores indicate worse pain.

Time frame
At predetermined time points after surgery at ( 2h,6h,12h,18h,24h) during the first 24 hours postoperatively.
2

Total Postoperative analgesic Consumption

The total amount of rescue analgesia consumed during the first 24 hours after surgery will be recorded.

Time frame
First 24 hours postoperatively (one day).
3

Duration of sensory block

Duration of sensory block will be assessed as the time interval from completion of the nerve block to the first administration of rescue analgesia 24 hours postoperatively.

Time frame
From completion of the nerve block until the first administration of rescue analgesia24 hours postoperatively.
4

Heart rate

Heart rate will be recorded at predefined perioperative time points to assess hemodynamic stability from baseline before surgery until end of surgery.

Time frame
From baseline before the nerve block until the end of surgery.

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: