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NCT Number: NCT05723406

The Immunomodulatory Effect of Sugammadex After Total Hip Replacement Surgery Under Neuraxial Anaesthesia: a Pilot Study

Monocenter randomized controlled proof of principle study to investigate the effect of sugammadex at the end of total hip replacement surgery on the postoperative innate immune function

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Radboudumc

Nijmegen, 6500HB, Netherlands

About this study

Rationale: With infections being the number one complication after surgery, more research is aimed at therapeutic strategies that positively influence the postoperative immune dysregulation. In the search for reducing surgical stress by a deep neuromuscular block (NMB), our group recently found evidence that sugammadex, used to antagonize a deep NMB, may have an immunomodulatory effect. Ex vivo analysis showed that sugammadex counteracted the immunosuppressive effect of rocuronium, but even in absence of rocuronium it had a positive effect on cytokine production capacity.

Therefore, we now propose a clinical pilot study in patients planned for total hip surgery under neuraxial anaesthesia to further investigate whether sugammadex has beneficial immunomodulatory effects.

Primary objective: To investigate the effect of sugammadex on the postoperative innate immune function.

Study design: A blinded, randomized controlled pilot study

Study population: 20 adults scheduled for primary hip replacement surgery under neuraxial anaesthesia.

Intervention: Patients will be randomized between a group receiving sugammadex at the end of surgery and a group receiving placebo.

Primary endpoint: Postoperative innate immune function as reflected by ex vivo mononuclear cell cytokine production capacity upon whole blood lipopolysaccharide (LPS) stimulation.

Secondary endpoint: Postoperative innate immune function as reflected by DAMP release and circulating inflammatory cytokines, Quality of Recovery score (QoR-40) postoperative day 1, postoperative pain and analgesia consumption, 30-day postoperative (infectious) complications

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age of 18 years or older
  • Scheduled for total hip replacement surgery under neuraxial anesthesia
  • Scheduled for primary hip replacement surgery
  • Informed consent obtained

Exclusion criteria

  • Insufficient control of the Dutch language to read the patient information and to fill out the questionnaires
  • Mentally incapacitated patients
  • Known or suspected hypersensitivity to sugammadex
  • Deficiency of vitamin K dependent clotting factors or coagulopathy
  • Severe renal disease (creatinine clearance <30 ml/min), including patients on dialysis)
  • Severe liver disease (Child-Pugh Classification C)
  • Women who are or may be pregnant or currently breastfeeding
  • Women of childbearing potential who don't use adequate method of contraception
  • Severe vertebral column disorder
  • Chronic use of psychotropic drugs
  • Known hypertrophic obstructive cardiomyopathy, severe aortic valve stenosis or severe mitral valve stenosis
  • Chronic use of NSAID's, steroids or immunosuppressive drugs

Treatment and study plan

Sugammadex 100 MG/ML [Bridion]

Drug

8 mg/ml

Other names: Bridion

Placebo

Other

Sodium 0.9% 5 ml

Primary outcomes

  1. Postoperative innate immune function

    Time frame: Postoperative day 1

    Ex vivo cytokine production capacity (TNF-α, IL-6, IL-10, IL-1β) of mononuclear cells upon whole blood Lipopolysaccharide(LPS) stimulation

Secondary outcomes

  1. Postoperative innate immune function

    Time frame: 2 timepoints: At the start of surgery (±30 minutes after administration neuraxial anesthesia) and at the end of surgery (15 minutes after administration intervention/placebo medication)

    Ex vivo cytokine production capacity (TNF-α, IL-6, IL-10, IL-1β) of mononuclear cells upon whole blood Lipopolysaccharide(LPS) stimulation

  2. Postoperative innate immune function

    Time frame: 3 timepoints: Postoperative day 1, at the start of surgery (±30 minutes after administration neuraxial anesthesia) and at the end of surgery (±15 minutes after administration intervention/placebo medication)

    Circulating inflammatory cytokines (TNF-α, IL-6, IL-10)

  3. Postoperative innate immune function

    Time frame: 3 timepoints: Postoperative day 1, at the start of surgery (±30 minutes after administration neuraxial anesthesia), and at the end of surgery (±15 minutes after administration intervention/placebo medication)

    Danger associated molecular pattern (DAMP) release (Heat shock protein 70 (HSP 70), High mobility group box 1 (HMGB1))

  4. Pain and total analgesia consumption

    Time frame: During hospital admission up to 3 days postoperative

    Pain scores by numeric rating scale (NRS 0-10)

  5. Quality of Recovery

    Time frame: Postoperative day 1

    Quality of Recovery 40 (QoR-40) validated questionnaire score. 40 points (minimum: extremely poor quality of recovery) to 200 points (maximum: excellent quality of recovery)

  6. Postoperative complications

    Time frame: Postoperative day 30

    postoperative complications scored by Clavien-Dindo classification; grade 0 (no deviation from ideal) grade 5 (death of patient)

  7. Postoperative infectious complications

    Time frame: Postoperative day 30

    Postoperative infectious complications scored the definitions of the StEP-COMPAC group initiative

Sponsors and collaborators

Lead sponsor

Radboud University Medical Center

Other

Registry information

Acronym: MAGIC

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Feb 10, 2023
Registry last updated
Nov 28, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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