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Clinical and Genetic Factors on the Postoperative Recovery Time of General Anaesthesia

Clinical and Genetic Factors on the Postoperative Recovery Time of General Anaesthesia

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02822417
Enrollment
1453
Registered
2016-07-04
Start date
2016-06-01
Completion date
2017-12-31
Last updated
2018-07-10

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

Conditions

General Anesthesia

Keywords

Recover time

Brief summary

To evaluate the effect of clinical factors on the recovery time of postoperative anesthesia and the effect of genetic variation in gDNA on the recovery time of postoperative anesthesia.

Detailed description

Recovery time of postoperative anesthesia is an important index to reflect patient's postoperative health status. The investigators want to collect patients' clinical dates and their blood samples, then extract DNA from blood samples, acquire every patients' genetic variation information. Finally, acquiring the mathematical model of the influence of clinical factors and genetic factors on the recovery time after operation, predicting the recovery time of anesthesia.

Interventions

None listed

Sponsors

Yijing He
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

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

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 delivered 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 anesthesiawithin 24 hours

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026