← Back to Clinical Trials
Recruiting NCT06633848

NCT06633848 Establishment of Clinical Prediction Model for Postoperative Symptomatic Spinal Epidural Hematoma

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06633848
Status Recruiting
Phase —
Sponsor Peking University Third Hospital
Condition Spinal Epidural Hematoma
Study Type OBSERVATIONAL
Enrollment 2,000 participants
Start Date 2025-01-01
Primary Completion 2026-12-31

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type OBSERVATIONAL
Interventions
spinal surgery

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 2,000 participants in total. It began in 2025-01-01 with a primary completion date of 2026-12-31.

⚠ 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

The goal of this observational study is to establish a clinical prediction model based on artificial intelligence algorithms for patients with postoperative symptomatic spinal epidural hematoma(PSSEH) after spinal surgery. The investigators will collect the features of 2000 patients as the training set to train the models using AI algorithms, then recruit a prospective cohort of 2000 patients to test if the trained model is precise and consistent to predict the occurrence of PSSEH as well as to find out whether there is any new risk factor of PSSEH.

Eligibility Criteria

Inclusion Criteria: * patients who will receive spinal surgery from January 2025 to December 2026 at Peking University Third Hospital Exclusion Criteria: * patients with a history of lumbar trauma before admission; * patients who suffer from malignant tumor; * patients with systemic infection; * patients who quit the study midway

Contact & Investigator

Central Contact

Orthopedics Department of Peking University Third Hospital

✉ 2411210441@pku.edu.cn

📞 008618811597977

Frequently Asked Questions

Who can join the NCT06633848 clinical trial?

This trial is open to participants of all sexes, studying Spinal Epidural Hematoma. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06633848 currently recruiting?

Yes, NCT06633848 is actively recruiting participants. Contact the research team at 2411210441@pku.edu.cn for enrollment information.

Where is the NCT06633848 trial being conducted?

This trial is being conducted at Beijing, China.

Who is sponsoring the NCT06633848 clinical trial?

NCT06633848 is sponsored by Peking University Third Hospital. The trial plans to enroll 2,000 participants.

Related Trials

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: November 2026  ·  Data Methodology