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A single-center, large-sample, prospective clinical research study of postoperative headache after general anesthesia and analysis of influencing factors

A single-center, large-sample, prospective clinical research study of postoperative headache after general anesthesia and analysis of influencing factors

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100385
Enrollment
Unknown
Registered
2025-04-08
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-09-22

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

Conditions

Postoperative headache after general anesthesia

Interventions

investigation group:None

Sponsors

Northern Jiangsu People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patients who are to undergo surgical procedures under general anesthesia; 2.Sex is not limited; 3.18 years old <= age <= 80 years old; 4.ASA classification: I-II; 5.18 kg/m2 <BMI <30 kg/m^2; 6.Informed consent, voluntary participation in the trial, and informed consent signed by the patients themselves.

Exclusion criteria

Exclusion criteria: 1.A history of substance abuse as well as a history of drug use; 2.Participation in a clinical trial of another drug or device within 3 months prior to the screening period; 3.Use of therapeutic drugs (e.g., benzodiazepines, opioid analgesics)by the patient for various reasons (e.g., insomnia, pain, etc).within 3 months prior to the Screening Period that may have an impact on the outcome of the trial, etc; 4.Allergy or contraindication to anesthetic drugs or components thereof; 5.Prior psychiatric or neurological disorders (e.g., schizophrenia, mania, bipolar abnormality, psychosis, epilepsy, neuralgia, etc.)and a history of taking medications corresponding to the treatment of the corresponding psychiatric or neurological disorders (e.g., antidepressants, anxiolytics, convulsants, antiepileptic drugs, etc.); 6.Women during pregnancy; 7.Patients with severe communication disorders due to severe hearing deterioration and other reasons; 8.Refusal to participate in this study; 9.Those deemed unsuitable by the investigator.

Design outcomes

Primary

MeasureTime frame
Incidence, severity, duration and headache of POH;Severity of POH;Duration of POH;Headache;

Countries

China

Contacts

Public ContactHaixia Xue

Northern Jiangsu People's Hospital

tagxhx@163.com+86 180 5106 0185

Outcome results

None listed

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