Clinical trial Recruiting at 1 site Interventional Ages 50 to 90

Managing blood pressure and using dexamethasone during lung cancer surgery

Official title: Impact of Intraoperative Blood Pressure Management and Dexamethasone on Patient's Outcomes After Lung Cancer Surgery: A 2 × 2 Factorial Randomized Controlled Trial

Run by Peking University First Hospital · NCT04209218 · Data updated 2026-11-12

This study is testing if managing blood pressure and giving dexamethasone during lung cancer surgery can help patients recover better and live longer.

Quick facts

Study typeInterventional
Ages50 Years to 90 Years
SexAll
Enrollment1988 (estimated)
SponsorPeking University First Hospital
Academic / other
Locations1 site (Beijing, Beijing Municipality)
StatusRecruiting
StartedApril 7, 2020
Main results expectedDecember 2026
Study endsDecember 2029
Registry record updatedJuly 31, 2025
Trial IDNCT04209218 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are patients aged 50 to 90 with resectable primary non-small cell lung cancer scheduled for radical surgery lasting more than two hours.

Probably not a fit

Patients with non-resectable lung cancer, recurrent or metastatic disease, or those with uncontrolled hypertension may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates how intraoperative blood pressure management and the administration of dexamethasone affect outcomes for patients undergoing surgery for non-small cell lung cancer (NSCLC). It focuses on the relationship between blood pressure fluctuations during anesthesia and postoperative complications, as well as the potential benefits of dexamethasone in reducing inflammation and improving recovery. The study aims to determine if tailored blood pressure management can enhance both early and long-term survival rates in these patients. Participants will be monitored for various outcomes related to their surgery and recovery.

Why it matters

Potential benefit: If successful, this approach could lead to improved survival rates and reduced complications for lung cancer surgery patients.

How similar studies have gone: Previous studies have shown promising results with individualized blood pressure management in surgical settings, suggesting potential for success in this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Aged \>50 years but \<90 years.
* Diagnosed as resectable primary non-small cell lung cancer (stage IA-IIIA) and scheduled for radical surgery with an expected duration of \>2 hours.
* Agree to participate in this study and sign the informed consent.

Exclusion Criteria:

* Clinical examinations suggest non-resectable lung cancer or patients scheduled for a biopsy surgery.
* Recurrent or metastatic lung cancer.
* History of cancer or complicated with cancer in other organs.
* Long-term exposure to glucocorticoids or other immunosuppressant(s) due to autoimmune disease or organ transplantation.
* Uncontrolled hypertension (systolic blood pressure \>180 mmHg or diastolic blood pressure \>110 mmHg); or requirement of vasopressors to maintain blood pressure.
* Persistent atrial fibrillation, or acute cardiovascular events (acute coronary syndrome, stroke, or congestive heart failure) within 3 months.
* Severe hepatic dysfunction (Child-Pugh C) or renal failure (requirement of renal replacement therapy).
* Any other circumstances considered unsuitable for study participation by attending physicians or investigators.

Where it's running

  • Department of Anesthesiology and Critical Care Medicine, Peking University First Hospital
    Beijing, Beijing Municipality, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.