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Study of esketamine in percutaneous transforaminal endoscopic discectomy

Study of esketamine in percutaneous transforaminal endoscopic discectomy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086959
Enrollment
Unknown
Registered
2024-07-16
Start date
2024-07-20
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

lumbar disc herniation

Interventions

Group A esketamine group:Preoperative loading dose: 0.2mg/Kg, intraoperative maintenance dose: 0.3mg/Kg/h
Group B control group:Equal amount of physiological saline solution

Sponsors

Ethics Committee of The General Hospital of Western Theater Command
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Lumbar disc herniation accompanied by obvious symptoms of nerve root compression, 2. Non surgical treatment for more than three months without significant relief 3. According to imaging examination, the location and segment of lumbar disc herniation are consistent with the symptoms 4. Single segment lumbar disc herniation 5. ASA classification level I or II; 6. Age greater than 18 years old and less than 80 years old

Exclusion criteria

Exclusion criteria: 1. Accompanied by lumbar instability or severe lumbar spinal stenosis 2. Developmental abnormalities 3. Tumors or infections 4. Patients who cannot tolerate prone position local anesthesia surgery 5. Patients with dysfunction of solid organs such as heart and lungs 6. Individuals with abnormal coagulation function 7. Allergic to medication 8. Mental abnormalities, inability to communicate and cooperate 9. Patients with uncontrolled hypertension or elevated intracranial pressure

Design outcomes

Primary

MeasureTime frame
Visual Analog Scale;Mean Arterial Pressure;Heart rate;Blood oxygen saturation (SpO2);Sedation score;systolic pressure;diastolic pressure;

Secondary

MeasureTime frame
Postoperative VAS score of lumbar ;Postoperative VAS score of lower limbs;

Countries

China

Contacts

Public ContactHaiyu Fu

The General Hospital of Western Theater Command

fuhaiyu2004@163.com+86 134 3880 3146

Outcome results

None listed

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