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A clinical study on magnesium sulfate in preventing perioperative atrial fibrillation in elderly patients undergoing anatomic pulmonary resection

A clinical study on magnesium sulfate in preventing perioperative atrial fibrillation in elderly patients undergoing anatomic pulmonary resection

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068046
Enrollment
Unknown
Registered
2023-02-05
Start date
2023-02-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

peri-operative new onset atrial fibrillation

Interventions

Control:intravenous 100ml N.S. before operation
Magnesium (M):ivgtt 80mg/kg magnesium diluted to 100ml N.S.

Sponsors

Shanghai Pulmonary Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients undergoing anatomic pulmonary resection under general anesthesia; 2. ASA class I~III; 3. Age is over or equal to 65 years old; 4. Blood routine, liver and kidney function, blood coagulation, electrocardiogram, cardiac ultrasound, blood gas analysis have been monitored; 5. Those who signed the informed consent form were approved by the hospital ethics committee.

Exclusion criteria

Exclusion criteria: 1. Renal insufficiency; 2. Have experienced any type of arrhythmia in the past 6 months or the patient is currently taking any antiarrhythmic drugs; 3. Hypermagnesaemia (> 1.25 mmol/L); 4. Allergy to magnesium sulfate; 5. FEV1<=1L; 6. The patient had undergone thoracic surgery; 7. Bilateral lung resection; 8. For other reasons, the researchers find it unsuitable to participate in the clinical trial.

Design outcomes

Primary

MeasureTime frame
incidence of peri-operative new onset atrial fibrillation;

Secondary

MeasureTime frame
hypotension;bradycardia;hypertension;Other types of arrhythmias;blush;Postoperative respiratory depression (< 8 beats/min);Gastrointestinal reactions (bloating, constipation, nausea, vomiting);Length of stay in ICU (hours) and total length of stay (days);Patients who visited any health care facility for arrhythmia within 3 months after surgery;In-hospital mortality and all-cause mortality at 3 months after surgery;

Countries

China

Contacts

Public ContactJin Shuqing

Shanghai Pulmonary Hospital

jinshuqing1@163.com+86 158 0210 8819

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026