Skip to content

Correlation between Intraoperative Hemodynamic Trajectory Changes during General Anesthesia and Postoperative Rehabilitation Outcomes after Aneurysm Embolization

Correlation between Intraoperative Hemodynamic Trajectory Changes during General Anesthesia and Postoperative Rehabilitation Outcomes after Aneurysm Embolization

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129184
Enrollment
Unknown
Registered
2026-07-31
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intracranial Aneurysm

Interventions

Intracranial Aneurysm Group:None

Sponsors

The First Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years; 2. Patients diagnosed with intracranial aneurysm and scheduled to undergo endovascular aneurysm embolization; 3. The procedure was performed under general anesthesia, with continuous and traceable intraoperative hemodynamic data recorded (e.g., arterial blood pressure, heart rate, etc., with a sampling interval of <= 5 minutes); 4. Complete clinical medical records were available, enabling access to all variables required for the study; 5. Complete postoperative rehabilitation outcome assessments were available, including short-term outcomes (e.g., recovery quality, complications, length of hospital stay) and long-term follow-up data (e.g., modified Rankin Scale score and Glasgow Outcome Scale score at 3 or 6 months postoperatively).

Exclusion criteria

Exclusion criteria: 1. Patients who underwent concurrent other surgical procedures during the same operation (e.g., craniotomy clipping, decompressive craniectomy, etc.) or whose procedure was converted to open craniotomy; 2. Patients with incomplete intraoperative hemodynamic data records, missing data at critical time points, or documented significant recording errors; 3. Patients with missing postoperative follow-up data, precluding evaluation of the primary rehabilitation outcome measures; 4. Pregnant patients; 5. Patients with pre-existing severe neurological dysfunction; 6. Patients with other severe comorbidities with an expected survival of less than 6 months.

Design outcomes

Primary

MeasureTime frame
The modified Rankin Scale (mRS) score at 3 months postoperatively was used to assess functional outcomes;

Secondary

MeasureTime frame
Wake-up quality;Complications during hospitalization;

Countries

China

Contacts

Public ContactWenwen Du

The First Affiliated Hospital of Wenzhou Medical University

862892574@qq.com+86 15088925016

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026