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Impact of Perioperative Body Temperature on Postoperative Complications and Pain in Video-assisted Thoracoscopic Surgery Patients Utilizing Continuous Temperature Monitoring

Impact of Perioperative Body Temperature on Postoperative Complications and Pain in Video-assisted Thoracoscopic Surgery Patients Utilizing Continuous Temperature Monitoring: A Prospective Cohort Study

Source: ClinicalTrials.gov · Last updated 26 Nov 2025

Brief summary (registry, in English)

A report from the National Cancer Center (published in JNCC) shows that lung cancer has the highest rates of both new cases and deaths in China. Surgery using a tiny camera (thoracoscopic surgery) is a main treatment for early-stage lung cancer. However, this type of chest surgery carries a much higher risk of patients developing low body temperature during the operation compared to other surgeries. This is because: (1) The surgery is complex and takes longer; (2) The chest cavity is open and exposed to the cool operating room air; (3)General anesthesia affects the brain's ability to regulate temperature and widens blood vessels, causing faster heat loss.Studies show that low body temperature happens in about 65-73% of these chest surgeries, while the average for surgeries longer than 2 hours nationwide is only about 40%. Low body temperature during surgery isn't just a problem at the time. It also increases the risk of negative outcomes after surgery. As known, it worsens post-surgery pain and increases risks of complications, such as infections, heart problems and bleeding issues. A common pain control technique for chest surgery is injecting local anesthesia medicine near the spine (Thoracic Paravertebral Block or TPVB). This technique is very effective at reducing pain after surgery, both short-term and long-term. However, new research suggests this nerve block might cause blood vessels to widen, potentially making patients lose body heat faster during surgery. Because TPVB is used so often, it's hard to tell if low body temperature during surgery directly causes worse pain afterwards, or if the nerve block itself influences both temperature and pain. The potential connection between low temperature caused by TPVB and later pain is not yet clear. The objective of this study is to investigate how low body temperature during and around the time of surgery affects complications after surgery (such as infections, heart and lung problems, longer hospital stays, etc.) in patients undergoing thoracic surgery. The investigators also aim to find the relationship between low body temperature during surgery and the occurrence of pain after surgery.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
144 (estimated)
First submitted
26 Sept 2025
Start date
1 Jan 2026
Primary completion date
31 Dec 2027
Lead sponsor
Peking University People's Hospital
Diseases
Lung cancer
NCT number
NCT07251439

What you commit to

  • Study type: Observational
  • Planned participants: 144
  • From 1 Jan 2026 to the primary completion date, 31 Dec 2027
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Emergency surgery or conversion to thoracotomy
  • Planned surgery \<1 hour or requiring cardiopulmonary bypass

Other

  • ASA ≥ IV
  • Preoperative fever (\>37.5°C) or hypothermia (\<36.0°C)
  • Chronic pain or opioid use ≥ 3 months
  • Immunosuppression
  • Thyroid dysfunction
  • Neurological dysfunction affecting pain assessment
  • Failed regional block (sensory block not covering T2-T8 at 4h postoperation)

Who the study is looking for

  • American Society of Anesthesiologist (ASA) I - III
  • BMI 18.5 - 30 kg/m²
  • Scheduled for Video-assisted thoracoscopic surgery (VATS) lung/mediastinal tumor resection (duration ≥1 hour)
  • General anesthesia with regional block (thoracic paravertebral block and serratus anterior plane block)
  • Written informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.