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Depth of Neuromuscular Blockade and the Perioperative Conditions in Laparoscopic Surgery in Pediatric Population

Deep Neuromuscular Blockade During Laparoscopic Surgery in Pediatric Patient and the Impact of the Depth of the Blockade on the Surgery Conditions, Perioperative Complications and Surgeon Satisfaction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02546843
Acronym
PedLapBlock
Enrollment
66
Registered
2015-09-11
Start date
2015-12-31
Completion date
2019-05-31
Last updated
2019-05-20

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

Conditions

Neuromuscular Blockade

Keywords

rocuronium, sugammadex, pediatric anesthesia, cisatracurium, surgical conditions

Brief summary

This randomized study prospectively evaluates our experience with administration of cisatracurium and rocuronium antagonized by sugammadex and evaluates the effects of various depths of neuromuscular blockage on providing optimal surgical conditions during laparoscopy with low-pressure capnoperitoneum.

Detailed description

This randomized study prospectively evaluates our experience with administration of cisatracurium and rocuronium antagonized by sugammadex and evaluates the effects of various depths of neuromuscular blockage on providing optimal surgical conditions during laparoscopy with low-pressure capnoperitoneum. After meeting inclusion criteria the patients will be randomized - - use of opaque envelopes, randomization into groups A and B in an operating theatre, study blinded for the patient (or his/her legal guardian) and surgeon. Group A - muscle relaxation using rocuronium followed by sugammadex reversal (in a dose according to TOF - (train-of-four) 2-4mg/kg), depth of muscle relaxation TOF 0 PTC (post-tetanic count) 0-1 Group B - muscle relaxation using cisatracurium followed by decurarization (neostigmine 0.03 mg/kg and atropine 0.02 mg/kg) Anesthesia management: * intravenous cannulation, preoxygenation, sufentanil 0.2 μg/kg intravenously, propofol 2.0mg/kg and in Group A - rocuronium 0.6 mg/kg (1 mg/kg only in a case of a rapid sequence induction), in Group B - cisatracurium 0.15mg/kg * orotracheal intubation, combined anesthesia using sevoflurane - MAC (minimal alveolar concentration) 1.0 with respect to the age of the patient * ventilation: PCV (pressure-controlled ventilation ), PEEP (positive end-expiratory pressure) +5 cm H2O (aqua), normocapnia, FiO2 (fraction of inspired oxygen ) 1.0 until the intubation, afterwards 0.4 + AIR * nasogastric tube placement Management of neuromuscular blockade: Group A - maintaining of deep muscular blockage - according to TOF 0, PTC 0-1, boluses of rocuronium 0.3 mg/kg are allowed Group B - maintaining of muscular relaxation TOF 1, boluses of cisatracurium 0.03 mg/kg are allowed Laparoscopy - capnoperitoneum pressure - 10 mmHg with a reduction to 8 mmHg if possible During the surgery the surgical conditions will be scored by using Surgical scoring system: (1-2 surgeons involved): 1. Optimal conditions: there is a wide laparoscopic field, no movements or contractions 2. Good conditions: there is a wide laparoscopic field with singular movements or muscle contractions 3. Acceptable conditions: there is a wide laparoscopic field but muscle contractions and/or movements occur regularly. Additional neuromuscular blocking agent is required. 4. Poor conditions: the same as in grade 3 and in addition, there is a hazard of tissue damage. 5. Extremely poor conditions: the surgeon cannot work because of weak muscle relaxation, the patient is coughing. Additional neuromuscular blocking agent is essential. Recovery from anesthesia: * extubation - TOF 0.9 - using sugammadex in Group A (2-4 mg/kg according to the depth of muscle relaxation) or decurarization in Group B (atropine 0.02 mg/kg and neostigmine 0.03mg/kg) * after standard 2-hour monitoring in the recovery room (heart rate, blood pressure, SpO2 (oxygen saturation by pulse oximetry), level of consciousness, PONV), patients will be observed in the intensive care unit for at least 24 hours Statistical analysis: (provided by IBA MUNI - Institute of biostatistic and analyses by Masaryk University Brno, Czech Republic) * demographic parameters - age, gender, type and duration of surgery * induction to general anesthesia - time until intubation (recognition of the capnogram curve) * ventilation - changes in the inspiratory pressure during capnoperitoneum, increase of EtCO2 (end-tidal CO2) * capnoperitoneal pressure * surgical scoring system

Interventions

DRUGRocuronium

rocuronium 0.6 mg/kg intravenously (1 mg/kg only in a case of a rapid sequence induction)

DRUGCisatracurium

cisatracurium 0.15mg/kg intravenously

DRUGNonspecific Neuromuscular Blockade reversal

neostigmine 0.03 mg/kg and atropine 0.02 mg/kg intravenously

DRUGSpecific Neuromuscular Blockade reversal

Sugammadex intravenously aimed to reverse the neuromuscular blockade.According to neuromuscular blockade monitoring: at TOF - (train-of-four) 2m g/kg, if TOF 0 and PTC(post-tetanic count) 0-1 4mg/kg of sugammadex will be administered

DRUGmaintaining the depth of neuromuscular blockade - rocuronium

repeated boluses of rocuronium 0.3 mg/kg will be administered to maintain the muscular blockage - according to TOF 0, PTC 0-1

DRUGmaintaining the depth of neuromuscular blockade - cisatracurium

repeated boluses of cisatracurium 0.03 mg/kg will be administered to maintain the muscular blockage - according to TOFmaintaining of muscular relaxation TOF 1

Sponsors

KDCHOT FN Brno
CollaboratorUNKNOWN
Brno University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* pediatric patients aged 2 to 17 years (+ 364 days) eligible for laparoscopy (diagnostic laparoscopy, appendectomy, cholecystectomy, nephrectomy, splenectomy, tumor biopsy, varicocele correction, testicular retention) * fasting of at least 6 hours * ASA (American Society of Anesthesiology score) score 1 or 2 * signed informed consent of the legal guardian of the patient

Exclusion criteria

* disagreement of the patient or his/her legal guardian * serious comorbidities - renal or hepatic disorders * ASA score ≥ 3

Design outcomes

Primary

MeasureTime frameDescription
Surgical scoring systemintraoperativelyDuring the surgery the blinded surgeon will grade surgical conditions due to surgical scoring system

Secondary

MeasureTime frameDescription
Number of adverse eventsintraoperativelyThe adverse events will be monitored

Countries

Czechia

Outcome results

None listed

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