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NCT Number: NCT04209218

Intraoperative Blood Pressure Management and Dexamethasone in Lung Cancer Surgery

Surgery is the front-line therapy for non-small cell lung cancer (NSCLC) but postoperative complications remains high and patients' long-term outcome is still challenging. In addition to surgery, anesthetic management particularly intraoperative blood pressure management and use of dexamethasone may affect patients' early and long-term outcomes after surgery for NSCLC. This study aims to investigate the impact of intraoperative blood pressure management and dexamethasone administration on early and long-term outcomes in patients undergoing surgery for lung cancer.

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Key information

Age range

50 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Anesthesiology and Critical Care Medicine, Peking University First Hospital

Beijing, Beijing Municipality, 100034, China

Location status: Recruiting

Location contact

Dong-Xin Wang, MD, PhD

CONTACT

[email protected]

86 (10) 83572784

Dong-Xin Wang, MD, PhD

PRINCIPAL_INVESTIGATOR

Wen-Wen Huang, MD

SUB_INVESTIGATOR

Yi-Bin Hua, MD

CONTACT

[email protected]

86 (10) 83572460

About this study

Surgical resection is the main treatment for patients with non-small cell lung cancer (NSCLC) and continuous efforts have been made to evolve surgical strategies and techniques. It has been now been realized that perioperative period is characterized with profound changes and anesthesia management may also affect outcomes of patients after cancer surgery.

Even under well controlled conditions, blood pressure fluctuation frequently occurs during anesthesia and surgery. In previous studies, intraoperative hypotension was associated with increased risk of organ injuries (such as delirium, acute kidney injury, myocardial injury, and stroke) and higher 1-year mortality. Unpublished data showed that intraoperative hypotension was also associated with shortened long-term survival in patients after lung cancer surgery. In a recent trial, individualized intraoperative blood pressure management which avoided intraoperative hypotension decreased the incidence of postoperative organ injury when compared with routine practice. Avoiding intraoperative hypotension may also prolong survival after lung cancer surgery. However, evidences are lacking regarding this topic.

Dexamethasone is frequently used for prevention of postoperative nausea and vomiting. Studies showed that a single low-dose dexamethasone has anti-inflammatory effect and can regulate immune function. It has been shown that perioperative dexamethasone can improve analgesia after surgery. In retrospective studies, perioperative low-dose dexamethasone was associated with less wound infection and improved long-term survival in patients after surgeries for pancreatic and lung cancer. It is hypothesized that intraoperative dexamethasone may reduce postoperative complications and improve long-term survival after lung cancer surgery. Interventional studies are required to confirm this hypothesis.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Dexamethasone

Drug

Dexamethasone (10 mg/2 ml) is administered before anesthesia induction.

Other names: Glucocorticoids

Targeted blood pressure management

Other

Blood pressure is maintained within ±10% from baseline.

Placebo

Drug

Placebo (2 ml normal saline) is administered before anesthesia induction.

Other names: Normal saline

Routine blood presure management

Other

Blood pressure is maintained according to routine practice.

Primary outcomes

  1. Overall survival after surgery

    Time frame: Up to 5 years after surgery

    Overall survival after surgery

  2. Incidence of organ injury and complications within 5 days after surgery (sub-study).

    Time frame: Up to 5 days after surgery.

    Organ injury includes delirium, acute kidney injury and myocardial injury. Postoperative complications are generally defined as newly occurred medical conditions that are harmful to patients' recovery and required therapeutic intervention, i.e., grade II or above on the Clavien-Dindo classification.

Secondary outcomes

  1. Recurrence-free survival after surgery

    Time frame: Up to 5 years after surgery

    Recurrence-free survival after surgery

  2. Cancer-specific survival after surgery

    Time frame: Up to 5 years after surgery

    Cancer-specific survival after surgery

  3. Event-free survival after surgery

    Time frame: Up to 5 years after surgery

    Event-free survival after surgery

  4. Rate of intensive care unit (ICU) admission after surgery (sub-study)

    Time frame: During the day of surgery

    Rate of ICU admission after surgery

  5. Rate of ICU admission with endotracheal intubation after surgery (sub-study)

    Time frame: During the day of surgery

    Rate of ICU admission with endotracheal intubation after surgery

  6. Duration of mechanical ventilation in ICU after surgery (sub-study)

    Time frame: Up to 30 days after surgery

    Duration of mechanical ventilation in ICU after surgery

  7. Length of stay in ICU after surgery (sub-study)

    Time frame: Up to 30 days after surgery

    Length of stay in ICU after surgery

  8. Incidence of organ injury within 5 days after surgery (sub-study)

    Time frame: Up to 5 days after surgery

    Organ injury includes delirium, acute kidney injury and myocardial injury. Delirium is assessed with the 3-minute diagnostic assessment for CAM-defined delirium (3D-CAM). Acute kidney injury is diagnosed according to the KDIGO (Kidney Disease: Improving Global Outcomes) criteria. Myocardial injury is diagnosed according to the serum cardiac troponin I level (higher than upper normal limit of the hospital's clinical laboratory).

  9. Incidence of complications within 30 days after surgery (sub-study)

    Time frame: Up to 30 days after surgery

    Postoperative complications are defined as new-onset medical events that are harmful to patients' recovery and required therapeutic intervention, i.e., grade II or above on the Clavien-Dindo classification.

  10. Length of stay in hospital after surgery (sub-study)

    Time frame: Up to 30 days after surgery

    Length of stay in hospital after surgery

  11. Rate of 30-day all-cause mortality (sub-study)

    Time frame: Up to 30 days after surgery

    Death due to any cause within 30 days after surgery

Other outcomes

  1. Overall survival after surgery in cancer patients

    Time frame: Up to 5 years after surgery

    Overall survival after surgery in cancer patients

  2. Recurrence-free survival after surgery in cancer patients

    Time frame: Up to 5 years after surgery

    Recurrence-free survival after surgery in cancer patients

  3. Cancer-specific survival after surgery in cancer patients

    Time frame: Up to 5 years after surgery

    Cancer-specific survival after surgery in cancer patients

  4. Event-free survival after surgery in cancer patients

    Time frame: Up to 5 years after surgery

    Event-free survival after surgery in cancer patients

  5. 30-item quality of life in 1-, 2-, and 3-year survivors

    Time frame: At the end of the 1st, 2nd, and 3rd year after surgery

    Quality of life is assessed with the 30-item Core Quality of Life Questionnaire (QLQ-C30), which assess functioning and symptom scales. The score of each scale ranges from 0 to 100, with higher score indicating better function or worse symptom.

  6. 13-item quality of life in 1-, 2-, and 3-year survivors

    Time frame: At the end of the 1st, 2nd, and 3rd year after surgery

    Quality of life is assessed with the 13-item Quality of Life Questionnaire-Lung Cancer Module (QLQ LC-13), which assess symptom scales. The score of each scale ranges from 0 to 100, with higher score indicating worse symptom. The QLQ LC-13 is a supplementary questionnaire module to be employed in conjunction with the QLQ-C30.

  7. Pain score within 3 days after surgery (sub-study)

    Time frame: Up to 3 days after surgery

    Pain score is assessed with the Numeric Rating Scale, an 11-point scale where 0=no pain and 10=the worst pain.

  8. Subjective sleep quality score within 3 days after surgery (sub-study)

    Time frame: Up to 3 days after surgery

    Subjective sleep quality is assessed with the Numeric Rating Scale, an 11-point scale where 0=the best sleep and 10=the worst sleep.

Study contacts

Contact information is provided by the study sponsor or research team.

Dong-Xin Wang, MD, PhD

CONTACT

[email protected]

86 (10) 83572784

Wen-Wen Huang, MD

CONTACT

[email protected]

86 (10) 83572460

Sponsors and collaborators

Lead sponsor

Peking University First Hospital

Other

Registry information

Official study title

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

Important dates

Study start
2020
Primary completion
2026
Study completion
2029
First posted
Dec 24, 2019
Registry last updated
Jul 31, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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