Actively Recruiting

Phase Not Applicable
Age: 65Years +
All Genders
ID07632664

A Multicenter Clinical Study on a New Treatment Model Combining Surgical Techniques, Perioperative Care, and Postoperative Rehabilitation for Elderly Lung Cancer Patients

Led by Peking University People's Hospital · Updated on 2026-06-08

1000

Participants Needed

1

Research Sites

113 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to improve treatment for elderly patients with lung cancer by developing a comprehensive, whole-process care model. The study focuses on creating a large clinical registry with data from over 2000 patients across at least 30 centers. It seeks to build risk prediction models for surgery and to optimize surgical and perioperative treatments, integrating both Western and traditional Chinese medicine approaches. The goal is to enhance outcomes and personalize care for elderly lung cancer patients. Participants are assigned to one of three surgical treatment groups: standard lobectomy, segmentectomy, or wedge resection, each combined with mediastinal lymph node sampling. Patients are evaluated and stratified by tumor size and geriatric risk scores before surgery. Postoperative care includes tailored perioperative management based on minimal residual disease monitoring and biomarker results. The study also develops personalized rehabilitation plans supported by a multidisciplinary team and remote monitoring technology. Throughout the study, participants will undergo comprehensive assessments including geriatric evaluations, imaging, pathology, and biomarker testing. Researchers will monitor overall survival for up to five years after surgery and track major postoperative complications within 90 days. The trial includes regular follow-up visits to evaluate treatment safety, effectiveness, and rehabilitation progress. This long-term involvement aims to establish an optimized, integrated treatment model specifically for elderly lung cancer patients.

CONDITIONS

Brief Title

Clinical Study of a New Treatment Model for Elderly Lung Cancer Patients

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 65 years or older
  • Confirmed non-small cell lung cancer eligible for curative surgical resection
  • Complete preoperative geriatric comprehensive assessment data available
  • Able to complete planned surgery and long-term follow-up
  • Voluntarily signed informed consent form
Not Eligible

You will not qualify if you...

  • History of other malignant tumors within the past 5 years
  • Severe heart, liver, kidney, or lung dysfunction preventing thoracic surgery
  • Confirmed distant metastasis before surgery that prevents radical resection
  • Uncontrolled severe infection or obvious coagulation disorders
  • Severe psychiatric disorder or cognitive dysfunction interfering with treatment and follow-up
  • Refusal of random assignment and postoperative regular monitoring

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery

Duration - Surgery day

Participants undergo one of three types of lung cancer surgery: lobectomy, segmentectomy, or wedge resection, each combined with mediastinal lymph node sampling.

1 surgical visit (in-person)

Postoperative Follow-up

Duration - Up to 90 days postoperatively

Participants receive stratified adaptive perioperative management and personalized perioperative treatment based on postoperative minimal residual disease and biomarker status, with regular monitoring for complications and recovery.

Regular visits during the first 3 months post-surgery

Long-term Monitoring

Duration - Up to 5 years

Participants are followed to assess overall survival and long-term outcomes for up to 5 years after surgical resection.

Periodic follow-up visits over 5 years

Trial Site Locations

Total: 1 location

1

Peking University People's Hospital

Beijing, Beijing Municipality, China, 100044

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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