Overview

Clinical Study of the Effect of Methylprednisolone Combined

Status:
Not yet recruiting
Trial end date:
2021-12-30
Target enrollment:
0
Participant gender:
All
Summary
Through the design of RCT study, the preoperative use of drugs (methylprednisolone + dihydroxypropyltheophylline) as intervention measures, the patients undergoing thoracoscopic lobectomy as the main research object, through the comparison of two groups of patients with intraoperative respiratory dynamics index and postoperative complications, to explore a more effective perioperative management method.
Phase:
N/A
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Qianfoshan Hospital
Treatments:
Dyphylline
Methylprednisolone
Methylprednisolone Acetate
Methylprednisolone Hemisuccinate
Prednisolone
Prednisolone acetate
Prednisolone hemisuccinate
Prednisolone phosphate
Criteria
Inclusion Criteria:

- 1. After fully understanding the purpose and significance of the trial, the patients
voluntarily participated in the trial and signed the informed consent;

2. The type of operation was general anesthesia and thoracoscopic lobectomy;

3. Age 18-75 years old, including boundary value, gender is not limited;

4. BMI 18-26kg / m2;

5. ASA grade I-II; no mental disorder, normal consciousness, normal communication;

6. No contraindications of methylprednisolone and dihydroxypropyltheophylline.

Exclusion Criteria:

- 1. There were diseases of immune, endocrine, nervous and mental system before
operation, and serious dysfunction of heart, liver and kidney;

2. Take immunosuppressive drugs and non steroidal anti-inflammatory drugs before
operation;

3. Respiratory tract infection (cough, expectoration, suffocation, etc.) in recent 1
month; pneumonia, bronchitis, etc. on CT;

4. History of chronic pulmonary disease, including but not limited to asthma,
pulmonary abscess, tuberculosis, chronic bronchitis, etc;

5. FEV1 < 50%;

6. Oxygen saturation was lower than 90% and airway pressure was higher than 40 cm H20;

7. Continuous hypotension or hypertension during the operation; intraoperative blood
loss > 1000ml;

8. Allergic to methylprednisolone or dihydroxypropyltheophylline;

9. There are any other situations that the researchers think are not suitable for
inclusion.