Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00795392
Other study ID # NJMU200811010
Secondary ID NJFY0811008
Status Completed
Phase N/A
First received November 20, 2008
Last updated September 17, 2009
Start date November 2008
Est. completion date September 2009

Study information

Verified date September 2009
Source Nanjing Medical University
Contact n/a
Is FDA regulated No
Health authority China: Ethics Committee
Study type Observational

Clinical Trial Summary

Perioperative psychological care is increasingly recognized as an essential part in the surgical environment. Previous studies have developed a strategy to evaluate the psychological influence after operations and found that postoperative psychological states significantly associated with the outcomes of patients. However, preoperative evaluation of patients the physicians do thus far is mainly the physical status assessment following the scale of American Society of Anesthesiologists (ASA). Whether a full-scale evaluation of preoperative psychological status to surgical patients could be a predictor to postoperative outcomes or not is not still completely understood. The investigators hypothesized that the preoperative psychological assessment would be an important predictor to outcomes.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date September 2009
Est. primary completion date September 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Patients undergoing elective surgical operation

- Age from 18-65 years

Exclusion Criteria:

- Age <18 years or >65 years

- Not willing to participate in this study

- Patients from emergency department

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
ASA scale
ASA scale evaluation before operation
Full-scale psychological assessment
Full-scale psychological evaluation before operation

Locations

Country Name City State
China Nanjing Maternal and Child Health Care Hospital Nanjing Jiangsu

Sponsors (1)

Lead Sponsor Collaborator
Nanjing Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time of recovery Since the end of the operation (1 day) to six-month follow-up. No
Secondary Intraoperative consumption of drugs From the time of start of operation (0 min) to the end of the surgical procedures, this time will undergo alteration in different individuals Yes
Secondary Hospitalization days Time length of staying at hospital from the day of inpatient to discharge home, this time will undergo alteration in different individuals No
Secondary Life quality Since the end of the operation (1 day) to six-month follow-up. No
See also
  Status Clinical Trial Phase
Completed NCT04361799 - Perioperative Closed-loop Glucose Control N/A
Completed NCT01193972 - Decision Aid Development for Smokers Phase 1
Completed NCT02932397 - Efficacy of Propofol vs Placebo in the Prevention of Coughing During Emergence of General Anesthesia Under Desflurane N/A
Completed NCT00966186 - The Rotational Insertion Technique for ProSeal Laryngeal Mask Airway N/A
Completed NCT01856998 - Therapeutic Equivalence (TE) Study of Propofol 2% MCT Fresenius (MCT=Medium-Chain Triglycerides) Compared With Diprivan® in Patients Undergoing Elective Surgery Phase 3
Not yet recruiting NCT06344325 - ED90 of Fospropofol Disodium in Induction and Maintenance of Anesthesia Phase 4
Completed NCT03857750 - Neuromuscular Blocking Agents in the Elderly
Completed NCT00875134 - Testing of the Apnea Prevention Device Phase 1/Phase 2
Completed NCT00290108 - The Influence of Injection Rate on EEG Propofol Peak Effect as Measured by Bispectral Index N/A
Completed NCT04020887 - Telemedicine Control Tower for the Post-Anesthesia Care Unit N/A
Not yet recruiting NCT06039306 - Perioperative Immunonutrition Under Enhanced Recovery After Surgery N/A
Completed NCT00948597 - Development of PK/PD Model for Individualized Propofol Dosing N/A
Completed NCT00776880 - Does American Society of Anesthesiologists (ASA) Physical Status Scale Enough in Patients Assessment N/A
Completed NCT04089592 - Comparison Of Dexmedetomidine and Fentanyl In Attenuation Of Hemodynamic Response To Direct Laryngoscopy And Intubation In Patient Undergoing Laparoscopic Cholecystectomy. N/A
Not yet recruiting NCT03593252 - Bowel Preparation in Elective Pediatric Colorectal Surgery N/A
Not yet recruiting NCT04225702 - Effect Of Aspirin Preoperative on Postoperative Cognitive Dysfunction In Elderly Patients Undergoing Knee Arthroplasty
Recruiting NCT05647252 - General Decolonization With Octenisan® Set Before Elective Orthopedic Surgery Phase 3
Completed NCT00205244 - Preoperative Preparation for Children N/A
Completed NCT05392452 - Fully Closed-Loop Insulin Delivery in Abdominal Surgery (CLAB) N/A
Completed NCT03455413 - Quality of Perioperative Invasive Ventilation in PICU