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Reversal With Low Doses of Sugammadex in Patients Undergoing Non-cardiac Surgery

A Randomized Double Blind Trial Comparing Reversal With Low Doses Of Sugammadex aFter Rocuronium-induced Neuromuscular Block Under General Anesthesia in Patients Undergoing Non-cardiac Surgery(TOF TRIAL)

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03460509
Enrollment
144
Registered
2018-03-09
Start date
2018-08-31
Completion date
2019-12-31
Last updated
2018-05-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neuromuscular Block, Postoperative Residual Curarization

Brief summary

Neuromuscular blocking agents (NMBA) are among the most commonly used drugs during general anesthesia and may induce complete muscle paralysis.They are used clinically to facilitate endotracheal intubation and to optimize surgical working conditions. Incomplete recovery from non-depolarising NMBAs continues to be a common problem in modern postoperative care unit and is associated with significant risk of microaspiration and hypoventilation which leads to pulmonary complications.Recently effective reversal of neuromuscular blockade has been described by use of lower dose of sugammadex the recommended without providing adequate answer to whether the lower dose is safe enough to avoid recurrent block. Hypotheses: 1. Administration of sugammadex 0.25 mg/kg at TOF ratio 0.3 will successfully reverse (TOF=0.9) rocuronium induced neuromuscular block within 10 min. 2. Recurrent block (TOF ratio \< 0.9) does not occur after reversal with low dose sugammadex 0.25 mg/kg. The primary objective of this trial is to assess the dose-response characteristics of sugammadex in reversing rocuronium induced neuromuscular block and to identify the minimal effective dose Secondary objective is to assess the safety of different doses of sugammadex (recurrent block (TOF ratio \< 0.9) after reversal and the occurrence of adverse reactions) Sugammadex is a very expensive drug which limits its use i anaesthesia department. By optimising drug dosage it may have economic impact and contribute to a wider use of sugammadex to reverse neuromuscular block before extubation and thus avoid incomplete recovery. This may lead to less risk for postoperative pulmonary complications and thereby reduce morbidity and mortality after surgery.

Detailed description

Doses of study drug will be 0 mg/kg Ideal Body Weight (IBW), 0.25 mg/kg IBW, 0.50 mg/kg IBW, 1.0 mg/kg IBW and 2.0 mg/kg IBW. TOF will be measured every 10th second until full reversal.

Interventions

DRUGSugammadex

Dose-response

Sponsors

The Hospital of Vestfold
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Patient, both genders, undergoing any elective in-hospital surgical procedure under general anesthesia requiring rocuronium neuromuscular block. * ASA I-IV * Signed informed consent

Exclusion criteria

* Patient less than 18 years of age * Patient participating in another clinical study which could interfere with TOF trial. * Patient with neuromuscular disease * Patient from ICU * BMI \> 30.0 kg/m2 * Patient scheduled for local or regional anesthesia only * Patient undergoing general anesthesia without rocuronium * Patient with hypersensitivity to NMBAs or sugammadex. Also hypersensitivity to any active substance or to any of the following excipient: Hydrochloric acid 3.7% (to adjust pH) and/or sodium hydroxide (to adjust pH) Water for injections . * Renal dysfunction (GFR\<30 mL/min/1,73m2) * Hepatic dysfunction * Patient who have received sugammadex in the last 24 h. * Pregnant or breastfeeding woman. Women in childbearing age must have a negative pregnant test before inclusion. * Bradycardia (puls \<40) * Hypotension (Systolic BP \<90 mmHg)

Design outcomes

Primary

MeasureTime frame
The time from study drug administration to reaching a TOF ratio of 0.9.10 minutes

Secondary

MeasureTime frameDescription
Number of patient with reoccurrence of neuromuscular block after initial reversal to TOF ratio 0.9.20 minutes
Number of patients with adverse reactions in each groupuntil discharge - 3 daysAdverse reactions (anaphylactic reaction, flushing, urticaria, erythematous rash, (severe) hypotension (BPsyst\> 75 mmHg), tachycardia (heart rate\> 120 beats/min), bradycardia (heart rate \<40 beats/min), swelling of tongue, swelling of pharynx, bronchospasm)

Contacts

Primary ContactTayyba Aslam, MD
tayybaaslam@gmail.com004798097489
Backup ContactEspen Lindholm, MD, PHD
espen.lindholm@siv.no004792213346

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026