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Comparative study of the effects of dexmedetomidine and eschloroacetone on tourniquet related reactions and hemodynamics in patients with general anesthesia

Comparative study of the effects of dexmedetomidine and eschloroacetone on tourniquet related reactions and hemodynamics in patients with general anesthesia

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096399
Enrollment
Unknown
Registered
2025-01-22
Start date
2024-11-28
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Tourniquet associated hypertension

Interventions

Esketamine Group (S Group):After anesthesia induction (tracheal catheter fixation), esketamine was injected intravenously at a rate of 0.3mg?kg-1?h-1 until the tourniquet was released.
Dexmedetomidine group (Group D):After the end of anesthesia induction, dexmedetomidine was pumped for 20 minutes at a load dose of 0.5ug?kg-1, and then at an administration rate of 0.4ug?kg-1?h-1 unti
Normal saline group (N group):The same volume of sodium chloride injection pump is calculated according to the actual body mass of the patient.

Sponsors

Affiliated Hospital of Qingdao University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients who underwent knee surgery under general anesthesia combined with nerve block with pneumatic tourniquet in our hospital from October 2024 to October 2025 (total knee replacement, knee unicondylar surface replacement, arthroscopic anterior cruciate ligament reconstruction, and knee double compartment replacement) are expected to sign informed consent. They were randomly divided into esketamine group (group S), dexmedetomidine group (group D) and saline group (group N) according to random number table method. American Society of Anesthesiologists (ASA) Grade I to III, ages 18 to 80 years.

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1 Patients who did not receive formal antihypertensive therapy or whose blood pressure was poorly controlled, i.e., systolic blood pressure = 160 mmHg or = 90 mmHg, and/or diastolic blood pressure =100 mmHg; 2 The history of ropivacaine allergy, puncture site infection, serious coagulation disorders and other puncture contraindications; 3 Patients with severe chronic diseases such as systemic chronic pain disease and severe dysfunction of liver and kidney function. 4 The patient had severe sinus bradycardia (< 50 beats/min)

Design outcomes

Primary

MeasureTime frame
Incidence of tourniquet-related hypertension;Incidence of tourniquet shock;

Secondary

MeasureTime frame
Hemodynamic mean;blood gas analysis;The amount of medication to be used when the tourniquet is applied;

Countries

China

Contacts

Public ContactMa Chao

Affiliated Hospital of Qingdao University

69609397@qq.com+86 199 0639 8878

Outcome results

None listed

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