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Completed

NCT Number: NCT07003061

Sarcopenia and Neuromuscular Block in Gastrointestinal Cancer Surgery

This prospective observational study aims to evaluate the effects of sarcopenia on intraoperative neuromuscular block (NMB) in patients undergoing gastrointestinal cancer surgery. Adult patients scheduled for elective gastrointestinal cancer surgery will be grouped as sarcopenic or non-sarcopenic based on preoperative abdominal CT scans. Neuromuscular block parameters, including onset time, depth, duration, and recovery, will be objectively measured using TOF (Train-of-Four) monitoring. The study seeks to determine whether sarcopenia influences sensitivity to muscle relaxants and to contribute to individualized anesthesia management and patient safety.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Dr. Abdurrahman Yurtaslan Ankara Oncology Education and Research Hospital Clinic of Anesthesiology and Rea

Ankara, Yenimahalle, 06200, Turkey (Türkiye)

About this study

Sarcopenia, characterized by the loss of skeletal muscle mass and function, is a significant clinical parameter affecting both prognosis and perioperative management in patients with gastrointestinal (GI) cancer. It may alter the pharmacokinetic and pharmacodynamic properties of anesthetic agents, particularly neuromuscular blocking agents. This prospective observational study will be conducted at Dr. Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital between June 1, 2025, and September 1, 2025.

Adult patients (aged 18 and above) scheduled for elective GI cancer surgery who have undergone preoperative abdominal computed tomography (CT) will be included. Patients with neuromuscular diseases, those on chronic steroid or immunosuppressive therapy, or those with significant organ failure will be excluded. Preoperative CT images at the L3 vertebral level will be evaluated by a radiologist to determine sarcopenia status, and patients will be divided into sarcopenic and non-sarcopenic groups according to established cut-off values.

All patients will receive standard anesthesia monitoring, including TOF (Train-of-Four) neuromuscular monitoring. The study will not alter any treatment protocols. After administration of muscle relaxants during anesthesia induction, neuromuscular block parameters such as onset time, depth, duration, need for reversal agents, and recovery time will be recorded. Demographic data, comorbidities, laboratory findings, type of surgery, and details of muscle relaxant use will also be collected.

The primary objective is to compare intraoperative neuromuscular block parameters between sarcopenic and non-sarcopenic patients. Statistical analysis will be performed using appropriate parametric or non-parametric tests for continuous variables and chi-square tests for categorical variables. The study aims to provide evidence for individualized dosing of muscle relaxants and to improve patient safety in anesthesia practice for GI cancer surgery.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged between 18 and 75 years
  • Patients diagnosed with gastrointestinal system (GIS) cancer and scheduled for elective surgery
  • Patients who have undergone preoperative abdominal computed tomography (CT) imaging
  • Patients classified as American Society of Anesthesiologists (ASA) physical status I-III

Exclusion criteria

  • Patients with a history of neuromuscular diseases
  • Patients receiving chronic steroid or immunosuppressive therapy
  • Patients with electrolyte imbalance
  • Patients using medications that affect neuromuscular transmission
  • Patients with severe organ failure in the preoperative period (e.g., liver or renal failure)
  • Patients who refuse to participate in the study
  • Patients requiring emergency surgery
  • Patients using muscle relaxants in the preoperative period

Treatment and study plan

Standard anesthesia management

Procedure

All patients will receive standard anesthesia care as per institutional protocols. No experimental intervention will be applied.

Primary outcomes

  1. Onset Time of Neuromuscular Block

    Time frame: Intraoperative (from induction until adequate block is achieved)

    Time from administration of the muscle relaxant to achievement of adequate neuromuscular block, measured by Train-of-Four (TOF) monitoring.

  2. Depth of Neuromuscular Block (TOF Ratio)

    Time frame: Intraoperative (from induction to end of surgery)

    Intraoperative depth of neuromuscular block, continuously monitored using TOF ratio.

  3. Duration of Neuromuscular Block

    Time frame: Intraoperative (from muscle relaxant administration to recovery)

    Time from administration of the muscle relaxant to recovery of neuromuscular function (TOF ratio ≥ 0.9).

  4. Dose and Duration of Reversal Agent

    Time frame: Intraoperative (from administration of reversal agent to recovery)

    Total dose and time required for the reversal agent to achieve recovery from neuromuscular block.

Sponsors and collaborators

Lead sponsor

Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital

Other

Registry information

Official study title

The Effects of Sarcopenia on Neuromuscular Block in Gastrointestinal Cancer Surgery

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jun 4, 2025
Registry last updated
Apr 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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