NCT05316545

Brief Summary

Using retrospective medical records to analyze the difference between the analysis of the correlation between operation time, blood loss, anesthesia methods, anesthesia medication, and postoperative recovery time

Trial Health

87
On Track

Trial Health Score

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

Enrollment
700

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Nov 2021

Shorter than P25 for all trials

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

November 16, 2021

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

January 10, 2022

Completed
3 months until next milestone

First Posted

Study publicly available on registry

April 7, 2022

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 15, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 15, 2022

Completed
Last Updated

November 7, 2023

Status Verified

December 1, 2021

Enrollment Period

12 months

First QC Date

January 10, 2022

Last Update Submit

November 5, 2023

Conditions

Orthognathic Surgery

Keywords

orthognathic surgeryanesthesiaretrospective analysis

Outcome Measures

Primary Outcomes (1)

  • medical treatment events performed

    The purpose of the study is to analyze the cases of orthognathic surgery in our hospital from 2010 to 2021 and find out which medical treatment events must be performed while maintaining Intentional hypotension such as inhaled anesthetics, pain relievers, Nitroglycerine, target controlled infusion, Precedex, Opioid, antagonist also the timing when the medical treatment intervene.

    During procedure

Secondary Outcomes (1)

  • time of anesthesia,lose of blood and recovery after surgery

    During procedure

Eligibility Criteria

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

Review the operation time, blood loss, anesthesia method, anesthesia medication, and postoperative recovery evaluation of the operation record sheet and anesthesia-related record sheet (including the recovery room and postoperative visit record sheet) in the patient's medical record.

You may qualify if:

  • Patients undergoing conventional anesthesia surgery and orthognathic surgery.

You may not qualify if:

  • Exclude the operation time greater than 8 hours.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kaohsiung Medical University Chung-Ho Memorial Hospital

Kaohsiung City, Sanmin Dist, 80756,, Taiwan

Location

Study Officials

  • Kuang-I Cheng, Phd

    Kaohsiung Medical University Chung-Ho Memorial Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 10, 2022

First Posted

April 7, 2022

Study Start

November 16, 2021

Primary Completion

November 15, 2022

Study Completion

November 15, 2022

Last Updated

November 7, 2023

Record last verified: 2021-12

Locations

TW(1)