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Effects of esketamine on postoperative analgesia and cognitive function in patients with radical cervical cancer surgery: a randomized controlled study

Effects of esketamine on postoperative analgesia and cognitive function in patients with radical cervical cancer surgery: a randomized controlled study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059492
Enrollment
Unknown
Registered
2022-05-02
Start date
2022-05-01
Completion date
Unknown
Last updated
2024-03-11

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

Conditions

postoperative pain

Interventions

Group 1 :Sufentanil and esketamine were administered for pain relief
Group 2:Postoperative analgesia was administered with sufentanil

Sponsors

Department of Anesthesiology, Affiliated Hospital of Southwest Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18-65 years old; 2. ASA score: I-II level; 3. BMI (kg/m2): 18-30; 4. Accept radical cervical cancer surgery under general anesthesia; 5. Have the ability to read and write, and can sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Opioids have been used before surgery; 2. Patients with mental illness; 3. There are any of the following contraindications for the use of esketamine injection: (patients with serious risk of elevated blood pressure or intracranial pressure; patients with intraocular hypertension, glaucoma or penetrating ocular trauma; patients with poorly controlled or untreated hypertension and resting systolic/diastolic blood pressure exceeding 180/110 mmHg; patients with untreated or undertreated hyperthyroidism); 4. Patients allergic to ketamine, propofol, opioids; 5. Patients with unstable ischemic heart disease; 6. Those who are unwilling or unable to use intravenous patient-controlled analgesia (PCIA) pumps; 7. Those who cannot use the pain Numerical Rating Scale (NRS); 8. Plan to enter the ICU after surgery; 9. Participated in clinical trials of other drugs as subjects in the past 3 months.

Design outcomes

Primary

MeasureTime frame
Visual pain score;Mini-Mental State Examination;Beck depression scale;

Countries

China

Contacts

Public ContactZhan Jian

Affiliated Hospital of Southwest Medical University

1119042327@qq.com+86 13551666643

Outcome results

None listed

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