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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02822417
Other study ID # 2016 MZ/CSU/PS
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2016
Est. completion date December 31, 2017

Study information

Verified date July 2018
Source Central South University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 1453
Est. completion date December 31, 2017
Est. primary completion date October 10, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Xiangya Hospital Central South University Changsha Hunan

Sponsors (1)

Lead Sponsor Collaborator
Yijing He

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Recover time of anesthesia within 24 hours
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