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The influence of esketamine on postoperative sleep disorders in patients with thyroid cancer

The influence of esketamine on postoperative sleep disorders in patients with thyroid cancer

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125182
Enrollment
Unknown
Registered
2026-05-22
Start date
2026-05-25
Completion date
Unknown
Last updated
2026-05-25

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

Conditions

Postoperative sleep disorders in patients with thyroid cancer

Interventions

Group L:Before anesthesia induction, 0.3mg/kg of esketamine was intravenously injected.
Group H:Before anesthesia induction, 0.5mg/kg of esketamine was intravenously injected.
Group C:Intravenous injection of an equal amount of normal saline before anesthesia induction

Sponsors

Affiliated Hospital of Zunyi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-60 years old, gender unrestricted; 2. ASA classification grade I - II; 3. BMI 18-28 kg/m^2; 4. Informed consent to the surgical and anesthesia plans, voluntarily signing the surgical informed consent form and the anesthesia informed consent form.

Exclusion criteria

Exclusion criteria: 1. Severe insomnia symptoms before the operation, with a preoperative Pittsburgh Sleep Quality Index (PSQI) > 7; 2. History of thyroid surgery, hyperthyroidism or hypothyroidism; 3. Severe organic lesions in heart, lung, liver and kidney functions [combined with abnormal functions of important organs such as heart, liver and kidney (NYHA classification > grade 2; liver failure or Child-Pugh score B or C; glomerular filtration rate < 30 ml/min)]; 4. Previously diagnosed with mental disorders; 5. Those with contraindications to general anesthesia and esketamine injection; 6. Long-term (at least 3 consecutive months) use of opioid drugs, sedative drugs, antidepressant drugs or anti-anxiety drugs; 7. Patients who refuse to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
Athens Insomnia , AIS;

Secondary

MeasureTime frame
Richards-Campbell Sleep , RCSQ;Hospital Anxiety and Depression ,HADS;Numerical Rating , NRS;

Countries

China

Contacts

Public ContactZhang Hong

Affiliated Hospital of Zunyi Medical University

2654885592@qq.com+86 188 9248 7959

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 30, 2026