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Comparison of Two Ways of Administration of the Neuromuscular Blockade in Thoracic Surgical Patients

Comparison of Two Ways of Administration of the Neuromuscular Blockade in Thoracic Surgical Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00018968
Enrollment
72
Registered
2019-10-10
Start date
2020-01-09
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Neuromuscular blockade

Interventions

Group 1: Continuous administration of Rocuronium, aiming a deep neuromuscular blockade (no answer to TOF-stimulation, number of twitches after PTC-stimulation between 1-5). When needed (for example b

Sponsors

Klinik für Anästhesiologie, Intensivmedizin und SchmerztherapieKrankenhaus Martha-Maria Halle Dölau
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - age over 18 years - elective thoracical surgery with resection of lung parenchyma (at least anatomical resection) - written informed consent to participate in the study

Exclusion criteria

Exclusion criteria: - age under 18 years - known allergy to rocuronium sugammadex - severe kidney impairment (GFR under 30) - significant liver disfunction - neuromuscular disorders - BMI above 35 kg/m2 - current use of antiepileptic agents, lithium or medication containing quinine - refusal to participate and the absence of written informed consent

Design outcomes

Primary

MeasureTime frame
Rating of surgical conditions using a rating scale

Secondary

MeasureTime frame
- overall dose of administrated rocuronium (mg/kg/min Operation) - the need and total number of additional boli of rocuronium - time elapsed between end of neuromuscular blockade and end of the operation - TOF/PTC-Count at the end of the operation, need of administration of the reversing agent sugammadex, dosis of administrated sugammadex (mg/kg) - the ability of the surgeon to tell to which group the operated patient belongs - practicability of the continuous administration of the neuromuscular blockade

Countries

Germany

Contacts

Public ContactKatalin Szentannai

Klinik für Anästhesiologie, Intensivmedizin und SchmerztherapieKrankenhaus Martha-Maria Halle Dölau

katalin.szentannai@martha-maria.de0345-5591416

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026