Comparing two methods of anesthesia for elderly patients
Ultrasound-assisted Versus Real-time Ultrasound-guided Combined Spinal-epidural Anesthesia Via a Paramedian Approach in Elderly Patients: a Randomized Controlled Study
This study is testing two different ways to give anesthesia to older patients to see which method works better and is safer for them.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 96 (estimated) |
| Ages | 60 Years and up |
| Sex | All |
| Sponsor | Tongji Hospital Academic / other |
| Locations | 1 site (Wuhan, Hubei) |
| Trial ID | NCT06241716 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the clinical effects of ultrasound-assisted localization and real-time ultrasound-guided combined spinal-epidural anesthesia in elderly patients. The research focuses on the paramedian approach to assess which method provides better outcomes in terms of efficacy and safety. By evaluating these two techniques, the study seeks to enhance anesthesia practices for older adults, who may have unique medical considerations.
Who should consider this trial
Good fit: Ideal candidates for this study are elderly patients aged 60 years and older with an ASA Grade I to III.
Not a fit: Patients with severe obesity, spinal deformities, allergies to local anesthetics, coagulation disorders, or communication barriers may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve anesthesia outcomes and reduce complications for elderly patients undergoing surgery.
How similar studies have performed: Other studies have shown promising results with ultrasound-guided anesthesia techniques, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Elderly patients (≥ 60 years old); * ASA Grade I to III. Exclusion Criteria: * Severe obesity (BMI\>35kg/m2); * Spinal deformity or surgical history; * Allergic to local anesthetics; * There are coagulation disorders; * Communication barriers
Where this trial is running
Wuhan, Hubei
- Tianzhu Liu — Wuhan, Hubei, China (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.