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Postoperative AnalgesiaPhase 1/2NCT07240402

Compare Morphine and Dexmedetomidine as Adjuvants to Bupivacaine in Ultrasound-guided ACB for Postoperative Analgesia After Knee Surgeries

A Phase 1/2 study testing Adductor Canal Block (ACB) Only in people with Postoperative Analgesia and Morphine and Dexmedetomidine, run by Kafrelsheikh University.

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Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

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Official record

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Trial summary

This study aims to compare morphine and dexmedetomidine as adjuvants to bupivacaine in ultrasound-guided ACB for postoperative analgesia after knee surgeries Read more about this study

Who is it for?
Any age
What is being tested?
Adductor Canal Block (ACB) Only
Could I receive a placebo?
No, everyone receives an active treatment
How many people
15 participants
Where
No sites listed yet
Study dates
17 Nov 2025to 1 Feb 2026
Phase
Phase 1/2

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 Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Both sexes.
  • American Society of Anesthesiologists (ASA) physical status I-II.
  • Body mass index (BMI) of 20-35 kg/m2.
  • Undergoing knee surgeries under spinal anesthesia.

Who cannot join

  • Any known allergy or contraindication to local anesthetic.
  • History of substance abuse.
  • Decompansated cardiac, pulmonary, hepatic, renal disease.
  • Obese patients with BMI>35kg/m2.
  • Pregnant and lactating mothers.
  • Coagulopathies.
  • Local skin infections at the site of injection.

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Ashraf Abd El-Nasser Abd El-Hamid kamel El Rewany Anesthesia KafrElsheikh University Faculty of Medicine Anesthesia, Surg, MBBCH contact

+201061195395

ashraf.elrewany2@gmail.com

About this study

Official title: Comparative Study of Morphine and Dexmedetomidine as Adjuvants to Bupivacaine in Ultrasound-Guided Adductor Canal Block for Postoperative Analgesia After Knee Surgeries

This study aims to compare morphine and dexmedetomidine as adjuvants to bupivacaine in ultrasound-guided ACB for postoperative analgesia after knee surgeries

Read the detailed description

Knee surgeries are frequently performed operations that can lead to intense pain after the procedure (1). Early mobilization following knee surgery is associated with improved functional outcomes and a reduction in postoperative complications. As a result, achieving effective pain relief while preserving motor function is a primary goal in postoperative care for knee procedures (2).

A variety of strategies are employed for managing postoperative pain, including systemic opioid administration, epidural anesthesia, peripheral nerve blocks, and local infiltration of anesthetics (3).

However, systemic opioids are linked to several undesirable side effects such as nausea, vomiting, itching, sedation, and respiratory depression, which may hinder rehabilitation.

Similarly, epidural analgesia often results in complications like hypotension, urinary retention, and pruritus. The use of long-acting intrathecal opioids has also been associated with adverse events including bilateral motor blockade, tremors, and hypotension. Due to these issues, the reliance on systemic and intrathecal methods for postoperative pain control has been declining (4).

The adductor canal block (ACB), which targets the Hunter's canal, anesthetizes the saphenous and vastus medialis nerves, along with partial coverage of other sensory nerves like the femoral nerve, medial cutaneous nerve, and branches of the obturator nerve as they traverse the distal canal (5). ACB is largely considered a sensory block, affecting only the motor nerve to the vastus medialis, making it advantageous in preserving quadriceps strength during recovery (6, 7). Bupivacaine, a widely used long-acting amide local anesthetic, is frequently employed in peripheral nerve blocks such as the ACB due to its favorable pharmacokinetics.

Nonetheless, its analgesic duration may be insufficient for managing postoperative pain in surgeries with high nociceptive intensity (8). To extend its efficacy and enhance analgesic quality, several adjunctive agents have been explored, including opioids and α2-adrenergic agonists (9).

Morphine, a traditional opioid analgesic, acts on μ-opioid receptors to prolong analgesia and reduce local anesthetic requirements. Despite its effectiveness, its use is limited by opioid-related adverse effects like nausea, vomiting, pruritus, and respiratory depression. Furthermore, some studies report that morphine may not significantly improve postoperative pain control or functional recovery after knee surgery (10-12).

Dexmedetomidine, a highly selective α2-adrenergic receptor agonist, has been increasingly studied as an adjuvant in peripheral nerve blocks. When administered

perineurally, it has demonstrated potential to accelerate onset, prolong analgesia, reduce postoperative pain intensity, and minimize systemic opioid use, all while producing fewer systemic side effects (13). Its peripheral analgesic properties are thought to result from direct binding to α2-receptors at the nerve site (14).

Currently, there is limited research directly comparing the efficacy of morphine versus dexmedetomidine as adjuvants to bupivacaine in ultrasound-guided ACB for postoperative analgesia following knee surgeries.

Being tested
Adductor Canal Block (ACB) Only
Keywords
Adductor Canal Block

What participants receive

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

  • Adductor Canal Block (ACB) OnlyDrug

    Also called adductor canal block

    This study aims to compare morphine and dexmedetomidine as adjuvants to bupivacaine in ultrasound-guided ACB for postoperative analgesia after knee surgeries. Primary outcome:

    • Time to first rescue analgesia .

    Secondary outcomes:

    • Total opioid consumption in 24 hours postoperatively.
    • Degree of pain using visual analogue scale (VAS).
    • Degree of patient satisfaction.
    • Incidence of complication A) Related to block Nerve Injury Vascular Puncture Hematoma B) Related to drug Local Anesthetic Systemic Toxicity (LAST)
Study groups in NCT07240402
Study groupRoleWhat they receive
Group DExperimentalPatients will receive ACB using 20 ml of bupivacaine 0.25%+ 0.5 µg/kg dexmedetomidine.
Receives: Drug: Adductor Canal Block (ACB) Only
Group MExperimentalPatients will receive ACB using 20 ml of bupivacaine 0.25% +0.1 mg/kg morphine.
Receives: Drug: Adductor Canal Block (ACB) Only
Group CExperimentalPatients will receive ACB using 20 ml of bupivacaine 0.25% alone as a control group.
Receives: Drug: Adductor Canal Block (ACB) Only

What is being measured

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

  1. Primary outcome:

    • Time to first rescue analgesia .

    Measured: 24 hours postoperatively.

Timeline

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

  1. First posted20 Nov 2025
  2. Study start17 Nov 2025 (estimated)
  3. Primary completion1 Jan 2026 (estimated)
  4. Study completion1 Feb 2026 (estimated)

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 1/2
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
15 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07240402
Sponsor's protocol ID
KafrelsheikhU
Status last verified
Nov 2025
First submitted
16 Nov 2025
Last updated
20 Nov 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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