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Effects of sugammadex on early postoperative recovery and pulmonary complications in patients undergoing thoracoscopic-laparoscopic radical esophagectomy

Effects of sugammadex on early postoperative recovery and pulmonary complications in patients undergoing thoracoscopic-laparoscopic radical esophagectomy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054381
Enrollment
Unknown
Registered
2021-12-16
Start date
2021-12-31
Completion date
Unknown
Last updated
2022-11-20

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

Conditions

Esophageal cancer

Interventions

Control group1:Intravenous neostigmine 0.04 mg/kg in combination with atropine 0.5 mg, while stopping intravenous pumping of anaesthetic drugs
Control group2:Intravenous neostigmine 0.04 mg/kg in combination with atropine 0.5 mg, with continued pumping of anaesthetic drugs
Experimental group:Intravenous sugammadex 2 mg/kg

Sponsors

Affiliated Cancer Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Select patients undergoing thoracoscopic laparoscopy combined with radical esophagectomy under general anesthesia; 2. Gender is not limited; 3. Aged 40 to 75 years; 4. ASA I-II grade.

Exclusion criteria

Exclusion criteria: 1. Body Mass Index (BMI) 25 kg/m2; 2. Systemic diseases such as coronary heart disease, asthma, nervous system diseases; 3. Severe cardiopulmonary insufficiency, American Heart Association (NYHA) cardiac function class >= grade III, severe dyspnea, cyanosis, abnormal respiratory rate; 4. Severe liver and kidney dysfunction; 5. Those who are allergic to sugammadex sodium, rocuronium bromide and neostigmine; 6. Pulmonary infection and atelectasis have been confirmed before surgery; 7. Patients with recurrent laryngeal nerve injury were identified before surgery; 8. Pregnant or lactating women; 9. Those who have used various oral contraceptives containing estrogen or progesterone within 1 month before surgery; 10. Patient refuses.

Design outcomes

Primary

MeasureTime frame
Residual neuromuscular block conditions;Time of extraction;Incidence of postoperative pulmonary complications;

Secondary

MeasureTime frame
Incidence of patients being transferred to ICU for observation and treatment;Post-operative recovery at 24H and 48H;Time of first post-operative bowel movement and defecation;Occurrence of postoperative bradycardia, nausea and vomiting and other adverse effects;Occurrence of complications such as paralytic intestinal obstruction;

Countries

China

Contacts

Public ContactLyu Shuaiguo

Affiliated Cancer Hospital of Zhengzhou University

lvshuaiguo1981@126.com+86 13623821823

Outcome results

None listed

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