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Effect of peri-operative magnesium sulfate infusion on inflammatory factors in patients with lung cancer

The effect of peri-operative magnesium sulfate infusion on inflammatory factors in patients with lung cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120305009213N5
Enrollment
44
Registered
2022-04-14
Start date
2020-09-22
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

Lung cancer. Malignant neoplasm of bronchus and lung

Interventions

Intervention 1: Control group: Standard protocol of anesthesia and surgery. Intervention 2: Intervention group: MgSO4 administration
in addition to standard cares, administration of MgSO4 made by Karmania Pars gene (KPG) company is added during induction of anesthesia (40 mg/kg within 10 minutes) and then infusion of maintenance do

Sponsors

Cancer institute
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with stage I (cT1N0 and cT2N0), stage II (cT1N1, cT2N1 and cT3N0) lung cancer Age 18 to 65 years old Candidate for lobectomy or pneumoectomy surgery Informed consent

Exclusion criteria

Exclusion criteria: History of severe heart disease, severe systemic and functional lung disease (asthma, COPD) Electrolyte disturbance BMI below 16 concurrent history of other cancers Albumin level less than 5.2 stage IIIA (cT3N1 and cT1–3N2) lung cancer and above Small cell carcinoma HIV positive or any immunodeficiency Patients undergoing clinical trial studies at the same time as this study Dissatisfaction with participating in the study Incomplete tumor resection (potential effect on cytokine levels) Long incision on chest wall, diaphragm or mediastinum Prescribing corticosteroids Pulmonary fibrosis (affected IL-8) History of chemotherapy and radiotherapy during the past month Patients with severe chronic renal failure (creatinine clearance less than 30 ml / min) Patients with acute renal failure and anuria Patients treated with drugs that produce hypermagnesemia (such as spironolactone, eplerenone)

Design outcomes

Primary

MeasureTime frame
Evaluation of blood levels of inflammatory (IL6, IL8) and anti-inflammatory (IL10, TGF-B) factors in the study groups. Timepoint: A blood sample is collected as a control immediately after induction of anesthesia and then another sample one day after surgery. Method of measurement: Using ELISA test.

Secondary

MeasureTime frame
Mortality rate. Timepoint: At the time of hospitalization up to 6 months after discharge. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahsa Hamidi Adl

Tehran University of Medical Sciences

dr.mahsa.hamidi@gmail.com+98 21 6119 0008

Outcome results

None listed

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