NCT02822417

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,453

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2016

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2016

Completed
29 days until next milestone

First Submitted

Initial submission to the registry

June 30, 2016

Completed
4 days until next milestone

First Posted

Study publicly available on registry

July 4, 2016

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 10, 2017

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2017

Completed
Last Updated

July 10, 2018

Status Verified

July 1, 2018

Enrollment Period

1.4 years

First QC Date

June 30, 2016

Last Update Submit

July 9, 2018

Conditions

General Anesthesia

Keywords

Recover time

Outcome Measures

Primary Outcomes (1)

  • Recover time of anesthesia

    within 24 hours

Study Arms (1)

patients after general anesthesia

Laparoscopic surgery, orthopedics surgery or open surgery patients after general anesthesia

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Laparoscopic surgery, orthopedics surgery or open surgery patients in Chinese

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Xiangya Hospital Central South University

Changsha, Hunan, 410008, China

Location

Biospecimen

Retention: SAMPLES WITH DNA

Samples with DNA retain 1 year

Study Officials

  • Yijing He, MD,PhD

    Xiangya Hospital of Central South University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Associate professor

Study Record Dates

First Submitted

June 30, 2016

First Posted

July 4, 2016

Study Start

June 1, 2016

Primary Completion

October 10, 2017

Study Completion

December 31, 2017

Last Updated

July 10, 2018

Record last verified: 2018-07

Locations

CN(1)