Clinical Study of the Effect of Methylprednisolone Combined (NCT04810819) | Clinical Trial Compass
UnknownNot Applicable
Clinical Study of the Effect of Methylprednisolone Combined
110 participantsStarted 2021-07-01
Plain-language 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.
Who can participate
Age range18 Years – 75 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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.
What they're measuring
1
Pplat
Timeframe: 5 different time points during the operation
2
Ppeak
Timeframe: 5 different time points during the operation