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A study for clinical and genetic factors on the postoperative recovery time of general anesthesia

Clinical and genetic factors on the postoperative recovery time of general anesthesia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ROC-16008731
Enrollment
Unknown
Registered
2016-06-28
Start date
2016-06-30
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

General anesthesia

Interventions

Case series:Nil

Sponsors

Xiangya Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged more than 18 years; 2. General anesthesia for all patients; 3. Patients underwent surgery for laparoscopic surgery, orthopedics surgery or open surgery; 4. Patients were not delivered allogeneic blood in three months; 5. Having the ability to understand and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Having an immune deficiency, as a patient with HIV infection; 3. Patients with infectious diseases, such as syphilis; 4. Patients dellivered allogeneic blood in three months; 5. Researchers believe that may increasing the risk of subjects or interfering clinical trial; 6. Don't have the ability to understand or sign the informed consent.

Design outcomes

Primary

MeasureTime frame
Recover time of anesthesia;—

Countries

China

Contacts

Public ContactYijing He

Institute of Clinical Pharmcology, Xiangya Hospital, Central South University

16656105@qq.com+86 15874812612

Outcome results

None listed

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