About this trial

This randomized controlled study aims to evaluate the effects of deep versus moderate neuromuscular blockade on intraoperative driving pressure and the development of postoperative critical respiratory events in patients undergoing abdominal surgery under general anesthesia.

Eligibility criteria

Qualifiers

Elective abdominal surgery under general anesthesia that is expected to last longer than one hour

ASA I-II-III

Age ≥18 years

Written informed consent

Disqualifiers

Refusal to participate in the study

ASA ≥ IV

Age <18

Obesity (BMI>30) and cachexia (BMI <18)

Trial design

Treatments tested in this trial

  • Rocuronium

Treatment groups

128 Participants
are divided into 2 treatment groups

Locations

1
Ankara Bilkent City Hospital06530, AnkaraÇankaya, Turkey (Türkiye)

Sponsors and collaborators

Ankara City Hospital Bilkent

Lead sponsor