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Effect of perioperative esketamine on postoperative inflammatory response in AIDS patients

Effect of perioperative esketamine on postoperative inflammatory response in AIDS patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097012
Enrollment
Unknown
Registered
2025-02-11
Start date
2024-05-10
Completion date
Unknown
Last updated
2025-02-17

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

Conditions

AIDS

Interventions

Experimental group:Intravenous esketamine 0.15 mg/kg + sufentanil 2µg/kg + esketamine 0.5mg/kg + ondansetron 8mg + 0.9% sodium chloride solution was mixed to 100mL for postoperative analgesia
Control group:sufentanil 2µg/kg+ondansetron 8mg +0.9% sodium chloride solution was mixed to 100mL for postoperative analgesia

Sponsors

Shenzhen Third People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Aged 18-60 years old, ASA I-II, BMI 18~30kg/m2. Diagnosed with human immunodeficiency virus (HIV) infection and AIDS before surgery, and was treated with high-activity-anti-retroviral-therapy (HAART) for more than 6 months, and the condition was stable, and anal fistula surgery was planned.

Exclusion criteria

Exclusion criteria: (1) Combined with severe anemia (Hb3s); APTT extension >10s; PLT<80*10^9/L (2) Patients who are currently being treated with opioids or other analgesics, or who have psychiatric disorders that affect pain scores, who use psychiatric drugs and are allergic to the components of the drugs used in this study, (3) Neuraxial anesthesia contraindications are also excluded, (4) Patients with contraindications to esketamine, such as those at serious risk of elevated blood pressure or intracranial pressure, patients with poorly controlled or untreated hypertension (arterial hypertension, resting systolic blood pressure/ Diastolic blood pressure greater than 180/100 mmHg); untreated or undertreated hyperthyroidism (hyperthyroidism)patients, etc. (see esketamine drug instructions for details). (5) Unable to complete the preoperative and postoperative evaluations or the treating physician is deemed unsuitable to participate in the study.

Design outcomes

Primary

MeasureTime frame
IL-6;TNF-a;

Secondary

MeasureTime frame
visual analogue scale, VAS;Ramsay score;Patient satisfaction scores;

Countries

China

Contacts

Public ContactWu Qiang

Shenzhen Third People's Hospital

wq2283@qq.com+86 186 2007 0099

Outcome results

None listed

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