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The antagonistic effect of deep muscle relaxation anesthesia combined with britine on perioperative complications of thyroid surgery

The antagonistic effect of deep muscle relaxation anesthesia combined with britine on perioperative complications of thyroid surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061475
Enrollment
Unknown
Registered
2022-06-26
Start date
2022-06-13
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Thyroid cancer

Interventions

Group 1:Deep muscle relaxation + britine antagonism
Group 2:Moderate muscle relaxation + neospermine antagonism

Sponsors

Fudan University Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18 to 65 years with no gender limitation; 2. ASA grade I or II; 3. Body mass index (BMI) <30kg/m^2; 4. Thyroid cancer patients; 5. Voluntarily participate and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Known allergy to the main drug or any excipient of the product; 2. The patient did not agree to receive recurrent laryngeal nerve monitoring; 3. Patients receiving medication that affects the effect of neuromuscular blockers; 4. Increased intracranial pressure or head injury; 5. Patients with low blood pressure, asthma (avoid using during the attack), epilepsy, neurological disease or neuromuscular disease; 6. Patients with expected difficult airway; 7. Preoperative liver and kidney function: abnormal alanine aminotransferase (ALT), aspartate aminotransferase (AST), urea nitrogen (BUN), creatinine (Cr) (ALT and AST were 1.5 times higher than the upper limit of normal, BUN and Cr were higher than the upper limit of normal); 8. Coronary heart disease, bronchial asthma, improperly controlled or difficult to control hypertension: systolic blood pressure (SBP) >=160mmHg or diastolic blood pressure (DBP) >=100mmHg; 9. Respiratory insufficiency and respiratory failure; 10. Patients who cannot express their wishes correctly; Poor compliance, unable to complete the experiment according to the study plan; 11. Participated in other drug trials within 30 days prior to enrollment; 12. Abnormal coagulation function; 13. The investigator did not consider it appropriate to participate in this study.

Design outcomes

Primary

MeasureTime frame
Postoperative sore throat;Swallowing time operation;Postoperative bleeding;The second step;Postoperative nausea and vomiting;

Secondary

MeasureTime frame
Rocuronium dosage;Visual analogue scale score;Satisfaction;Other adverse events;Sedation scores;

Countries

China

Contacts

Public ContactHou Wenting

Fudan University Cancer Hospital

13651873791@163.com+86 13651873791

Outcome results

None listed

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