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Effect of Cocktail Therapy with Different Doses of Adrenaline on Hemodynamics in Patients Undergoing Total Knee Replacement

Effect of Cocktail Therapy with Different Doses of Adrenaline on Hemodynamics in Patients Undergoing Total Knee Replacement

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063768
Enrollment
Unknown
Registered
2022-09-16
Start date
2022-09-15
Completion date
Unknown
Last updated
2023-04-17

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

Conditions

Osteoarthritis of the knee

Interventions

Group A:No adrenaline
Group B:Adrenaline 0.3 mg
Group C:Adrenaline 0.5 mg

Sponsors

Qilu Hospital of Shandong University (Qingdao)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years old, no language communication and cognitive impairment before operation; 2. Patients who are scheduled to undergo knee replacement; 3. American Society of Anesthesiologists ASA Class I, II, III; 4. Operated by the same joint surgeon team; 5. Clearly understand and voluntarily participate in the study, and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those who cannot cooperate with combined spinal epidural anesthesia, such as previous history of severe mental or neurological diseases, high bleeding risk, nerve damage, etc.; 2. The skin around the nerve block puncture point is infected; 3. Patients who are allergic to local anesthetics; 4. Patients who do not need a tourniquet during the operation; 5. Patients with atrial fibrillation or other arrhythmias before surgery, patients with unstable angina pectoris and a history of myocardial infarction before surgery; 6. Patients with post-traumatic arthritis, secondary arthritis or simultaneous bilateral total knee arthroplasty; 7. Participated in other clinical trials within 30 days; 8. Other reasons that the investigator thinks it is inappropriate to participate in the trial.

Design outcomes

Primary

MeasureTime frame
systolic pressure;

Secondary

MeasureTime frame
Other intraoperative hemodynamic indexes;Intervention of vasoactive drugs;Postoperative pain score;Wound drainage;Quadriceps muscle strength score;degree of satisfaction;hospital stay;

Countries

China

Contacts

Public ContactJinfeng Zhou

Qilu Hospital of Shandong University (Qingdao)

805617366@qq.com+86 18561812139

Outcome results

None listed

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