NCT06762184 Scores in Critically Ill Patients After Craniotomy
| NCT ID | NCT06762184 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Beijing Tiantan Hospital |
| Condition | Post-craniotomy |
| Study Type | OBSERVATIONAL |
| Enrollment | 1,600 participants |
| Start Date | 2024-11-01 |
| Primary Completion | 2025-03-01 |
Eligibility & Interventions
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 1,600 participants in total. It began in 2024-11-01 with a primary completion date of 2025-03-01.
⚠ 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 study planned to review patients admitted to three ICU wards at Beijing Tiantan Hospital between 2017 and 2020. It focused on adult patients who had undergone craniotomy and stayed in the ICU for more than 24 hours. Researchers intended to collect patient information, surgery details, complications, and outcomes from medical records. They also planned to gather routine scoring data used at the hospital and double-check its accuracy. Patients would be divided into two groups based on whether they survived or not, and the ability of different scoring systems to predict outcomes would be analyzed. Additionally, the study aimed to group patients by the type of surgery and assess how well the scoring systems predicted outcomes for each group.
Eligibility Criteria
Inclusion Criteria: * Patients admitted to the ICU wards between 2017 and 2020 * Patients underwent craniotomy * Patientshad an ICU stay of more than 24 hours Exclusion Criteria: * Pregnant or lactating women * Patients enrolled in other clinical studies
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06762184 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Post-craniotomy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06762184 currently recruiting?
Yes, NCT06762184 is actively recruiting participants. Contact the research team at zjfyanger@sina.com for enrollment information.
Where is the NCT06762184 trial being conducted?
This trial is being conducted at Beijing, Chile.
Who is sponsoring the NCT06762184 clinical trial?
NCT06762184 is sponsored by Beijing Tiantan Hospital. The trial plans to enroll 1,600 participants.