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Retrospective Clinical Study on Total Knee Replacement Patients and Hip Replacement Patients with General Anesthesia Combined with Plexus Block

Retrospective Clinical Study on Total Knee Replacement Patients and Hip Replacement Patients with General Anesthesia Combined with Plexus Block

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200059086
Enrollment
Unknown
Registered
2022-04-24
Start date
2022-06-01
Completion date
Unknown
Last updated
2024-02-11

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

Conditions

Total Knee Replacement Patients and Hip Replacement

Interventions

Test group:Nerve Block Anesthesia + General Anesthesia Combined Anesthesia
Control group:General anesthesia

Sponsors

The First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. The patient has no serious dysfunction of important organs, no systemic diseases such as cachexia, autoimmune or immunodeficiency diseases, infections, severe mental disorders, etc.; 2. Preoperative diagnosis clearly requires total knee arthroplasty or hip arthroplasty.

Exclusion criteria

Exclusion criteria: 1. Volunteers who participated in other drug clinical trials or other anesthesia treatment trials within 3 months before being selected for this study; 2. Telephone follow-up, patients who refused to accept this study; 3. This study excluded patients who had multiple organ resections or other fractures undergoing surgery at the same time; 4. Patients who have received organ transplantation; 5. Patients who have had a history of surgery and have had serious complications and a history of poor anesthesia surgery.

Design outcomes

Primary

MeasureTime frame
Surgery-related complications during perioperative period;Anesthesia-related complications during the perioperative period;Blood pressure;Heart rate;Oxygen saturation;Injection pain or not;Additional dose;Whether according to the two-dimensional code, regular preoperative preparation of bowel clearance;Actual bowel readiness;Satisfaction of endoscopists;Patient satisfaction;The results of the 7-day postoperative follow-up;

Countries

China

Contacts

Public ContactXian-Fu Lu

First Affiliated Hospital of Anhui Medical University

lxf0001@126.com+86 18256031820

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026