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Recruiting NCT07314762

NCT07314762 Elderly Patients Undergoing Surgery During Perioperative Period

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Clinical Trial Summary
NCT ID NCT07314762
Status Recruiting
Phase
Sponsor Second Affiliated Hospital of Wenzhou Medical University
Condition Postoperative Complications
Study Type OBSERVATIONAL
Enrollment 1,200 participants
Start Date 2023-12-30
Primary Completion 2030-12-30

Eligibility & Interventions

Sex All sexes
Min Age 65 Years
Max Age N/A
Study Type OBSERVATIONAL

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 1,200 participants in total. It began in 2023-12-30 with a primary completion date of 2030-12-30.

⚠ 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

The elderly patients have poorer overall conditions and have lower tolerance to trauma, anesthesia, and surgery. Therefore, the incidence of postoperative complications is relatively higher. In non-cardiac surgeries, approximately 20% of elderly patients experience postoperative complications, and the incidence of postoperative delirium (POD) is 23.8%. This may lead to prolonged hospital stays, increased hospital costs, and affect prognosis and even mortality. The investigators plan to conduct a prospective cohort study by systematically collecting biological samples and clinical information of elderly patients during the perioperative period to explore the possible risk factors and pathogenesis of postoperative delirium and postoperative complications in elderly surgical patients, and to construct a risk prediction model for postoperative complications.

Eligibility Criteria

Inclusion Criteria: 1\) Surgical patients aged 65 or above or non-surgical subjects aged 65 or above. 2) Agree to participate in this study and sign the informed consent form. Exclusion Criteria: 1)Refused to participate in the study.

Contact & Investigator

Central Contact

Ting Li MD. PhD

✉ liting1021@aliyun.com

📞 +86-135-8787-6896

Principal Investigator

Ting Li, MD. PhD

PRINCIPAL INVESTIGATOR

Department of Anaesthesiology and Perioperative Medicine, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China

Frequently Asked Questions

Who can join the NCT07314762 clinical trial?

This trial is open to participants of all sexes, aged 65 Years or older, studying Postoperative Complications. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07314762 currently recruiting?

Yes, NCT07314762 is actively recruiting participants. Contact the research team at liting1021@aliyun.com for enrollment information.

Where is the NCT07314762 trial being conducted?

This trial is being conducted at Wenzhou, China.

Who is sponsoring the NCT07314762 clinical trial?

NCT07314762 is sponsored by Second Affiliated Hospital of Wenzhou Medical University. The principal investigator is Ting Li, MD. PhD at Department of Anaesthesiology and Perioperative Medicine, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China. The trial plans to enroll 1,200 participants.

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