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Sugammadex vs Neostigmine/Glycopyrrolate on Urinary Retention After Spine Surgery

Phase 4
Conditions
Spine Surgery
Reversal of Neuromuscular Blockade
Urinary Retention Postoperative
Interventions
Registration Number
NCT05887375
Lead Sponsor
University of Missouri-Columbia
Brief Summary

This is an active-comparator controlled study to evaluate the effect of sugammadex compared to neostigmine/glycopyrrolate for reversal of rocuronium on the incidence of urinary retention after subjects undergo elective ambulatory spine surgery.

Detailed Description

Subjects requiring elective ambulatory posterior lumbar laminectomy, will receive either an intravenous infusion bolus of Sugammadex (2 mg/kg dosed by actual body weight) or intravenous infusion bolus of Neostigmine (50 μg/kg, up to 5 mg maximum dose) plus Glycopyrrolate (10 μg/kg, up to 1 mg maximum dose). Additionally, all subjects will receive hospital standard of care therapy for their surgery and hospital stay.

Recruitment & Eligibility

Status
ENROLLING_BY_INVITATION
Sex
All
Target Recruitment
118
Inclusion Criteria
  • Age ≥ 18 years
  • ASA Physical Status I-III
Exclusion Criteria
  • Inability to obtain written informed consent
  • Allergy to medications used in the protocol
  • Known or suspected neuromuscular disorders
  • Significant renal disease with a serum creatinine ≥ 2 mg/dL
  • Significant liver disease
  • A family history of malignant hyperthermia
  • History of genitourinary surgery, cancer, or radiation within the last year
  • Currently prescribed urological medications or diuretics
  • BPH or symptoms of BPH (interrupted or weak urine stream or wake up to urinate more than two times per night)
  • History or diagnosis of urinary incontinence or urinary retention
  • History of PONV with use of scopolamine
  • Use of Foley catheter pre- or intra- operatively
  • Perioperative medications that influence micturition (e.g., diuretics or intraoperative anticholinergic medication use other than NMB reversal)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Sugammadex 2 mg/kgRocuroniumSugammadex 2 mg/kg administered as a single intravenous (IV) dose.
Sugammadex 2 mg/kgSugammadexSugammadex 2 mg/kg administered as a single intravenous (IV) dose.
Neostigmine + GlycopyrrolateNeostigmineNeostigmine 50 μg/kg (up to 5 mg maximum dose) plus glycopyrrolate 10 μg/kg (up to 1 mg maximum dose) administered as a single IV dose.
Neostigmine + GlycopyrrolateRocuroniumNeostigmine 50 μg/kg (up to 5 mg maximum dose) plus glycopyrrolate 10 μg/kg (up to 1 mg maximum dose) administered as a single IV dose.
Neostigmine + GlycopyrrolateGlycopyrrolateNeostigmine 50 μg/kg (up to 5 mg maximum dose) plus glycopyrrolate 10 μg/kg (up to 1 mg maximum dose) administered as a single IV dose.
Primary Outcome Measures
NameTimeMethod
Incidence of urinary retentionUp to 6 hours after administration of study intervention

The difference between sugammadex and neostigmine/glycopyrrolate on the incidence of urinary retention defined as no void more than 6 hours after posterior lumbar spine surgery in ambulatory/short stay patients.

Secondary Outcome Measures
NameTimeMethod
MicturitionUp to 1 day after administration of study intervention

Between patients who received sugammadex and neostigmine/glycopyrrolate. To compare actual times of micturition we will analyze the proportion of patients (percentages) voided at 6, 9, 12 and 24 hours.

Length of hospital stayUp to 7 Days after administration of study intervention

Between patients who received sugammadex and neostigmine/glycopyrrolate. To compare length of hospital stay.

Urinary retention symptomsUp to 1 day after administration of study intervention

Between patients who received sugammadex and neostigmine/glycopyrrolate. To compare urinary retention symptoms, we will administer a questionnaire at 6 hours postoperatively and on postoperative day 1.

Bladder catheterizationUp to 1 Day after administration of study intervention

Between patients who received sugammadex and neostigmine/glycopyrrolate. To compare need for bladder catheterization (straight or Foley).

Bladder urine volumeUp to 6 hours after administration of study intervention

Between patients who received sugammadex and neostigmine/glycopyrrolate. To compare bladder urine volumes in milliliters (mL) we will perform bladder ultrasound scan at 6 hours postoperatively if patients did not void.

Trial Locations

Locations (1)

University Hospital

🇺🇸

Columbia, Missouri, United States

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