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Recruiting NCT06967207

NCT06967207 Electrical Impedance Tomography-Based Prognostic Model for ARDS

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Clinical Trial Summary
NCT ID NCT06967207
Status Recruiting
Phase
Sponsor XiaoJing Zou,MD
Condition Acute Respiratory Distress Syndrome (ARDS)
Study Type OBSERVATIONAL
Enrollment 625 participants
Start Date 2025-04-15
Primary Completion 2027-12-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 80 Years
Study Type OBSERVATIONAL
Interventions
Not applicable- observational study

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 625 participants in total. It began in 2025-04-15 with a primary completion date of 2027-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This multicenter, prospective, observational study aims to develop and validate an EIT-based prognostic model for ARDS. By focusing on the pathophysiological characteristics of ARDS and the causes of ventilator-induced lung injury, the investigators intend to establish a prognostic model that reveals lung injury and heterogeneity, enabling risk stratification and guiding individualized treatment.

Eligibility Criteria

Inclusion Criteria: 1. Meet the new 2023 ARDS global definition; 2. Age 18-80 years Exclusion Criteria: 1. Expected death within 24 hours of screening; 2. Metastatic cancer (active malignancy with distant metastases); 3. Severe psychiatric disorders; 4. Pregnancy or postpartum status; 5. Pneumothorax or moderate to large pleural effusion without adequate drainage; 6. Chronic respiratory failure; 7. Patients with pulmonary embolism or pulmonary hypertension; 8. Heart failure patients: EF \<50% or NYHA class III or IV; 9. Patient/family refusal to participate; 10. Participation in another interventional trial within 3 months prior to enrollment

Contact & Investigator

Central Contact

Xiaojing Zou Zou

✉ 249126734@qq.com

📞 84+13995518630

Frequently Asked Questions

Who can join the NCT06967207 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 80 Years, studying Acute Respiratory Distress Syndrome (ARDS). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06967207 currently recruiting?

Yes, NCT06967207 is actively recruiting participants. Contact the research team at 249126734@qq.com for enrollment information.

Where is the NCT06967207 trial being conducted?

This trial is being conducted at Guangzhou, China, Wuhan, China, Wuhan, China, Shanghai, China.

Who is sponsoring the NCT06967207 clinical trial?

NCT06967207 is sponsored by XiaoJing Zou,MD. The trial plans to enroll 625 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology