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Search / Trial NCT06334562

The Clinical Effect of Sugammadex Sodium (Domestic) for Antagonizing Neuromuscular Blockade After Thoracic Surgery

Launched by THE FOURTH AFFILIATED HOSPITAL OF ZHEJIANG UNIVERSITY SCHOOL OF MEDICINE · Mar 27, 2024

Trial Information

Current as of July 23, 2025

Recruiting

Keywords

Sugammadex Sodium Postoperative Neuromuscular Block Antagonism Thoracic Surgery

ClinConnect Summary

This clinical trial is studying two medications, sugammadex and neostigmine, to see which one is better at reversing muscle relaxation after lung surgery. When patients have surgery, they often receive muscle relaxants to help with anesthesia, but these need to be reversed afterward so patients can breathe normally again. The goal of the trial is to find out if sugammadex (a domestic version) works more effectively than neostigmine for this purpose.

To participate in this trial, patients must be 18 years or older, undergoing elective lung surgery that requires general anesthesia and a breathing tube, and will be given a muscle relaxant called rocuronium. Certain patients will not be eligible, such as those with specific allergies, severe health issues, or any factors that might complicate the surgery or recovery. If you join the trial, you can expect to receive either sugammadex or neostigmine after your surgery, and the results will help improve how muscle relaxants are managed in the future.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Patients who undergo elective lung surgery under general anesthesia and require endotracheal intubation;
  • 2. Age\>18 years old, gender not limited;
  • 3. American Society of Anesthesiologists ASA Level I-III;
  • 4. Use rocuronium bromide for neuromuscular blockade;
  • 5. The patient voluntarily participated in the trial.
  • Exclusion Criteria:
  • 1. The patient explicitly refused to participate in this trial;
  • 2. Family history of malignant hyperthermia, patients with allergies to sodium sulbactam, neostigmine ingredients and their excipients, and patients with allergies to drugs used during general anesthesia;
  • 3. Patients with tracheal malformations or suspected difficult airways, coagulation dysfunction, severe liver and kidney dysfunction, and severe lung disease;
  • 4. Patients who are not extubated and sent to the ward or ICU after surgery;
  • 5. The researchers believe that patients with any other unfavorable factors to participate in this trial.

About The Fourth Affiliated Hospital Of Zhejiang University School Of Medicine

The Fourth Affiliated Hospital of Zhejiang University School of Medicine is a leading clinical research institution dedicated to advancing medical knowledge and improving patient care through innovative clinical trials. With a strong emphasis on collaboration and interdisciplinary research, the hospital integrates cutting-edge technology and expert clinical practices to support a wide range of medical studies. Its commitment to ethical standards and patient safety ensures the highest quality of research outcomes, making it a trusted partner in the medical community for both national and international clinical trials.

Locations

Yiwu, Zhejiang, China

Patients applied

0 patients applied

Trial Officials

JianHong Xu

Principal Investigator

The Fourth Affiliated Hospital of Zhejiang University School of Medicine

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported