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Redesigned Process in the Operating Room

NCT01937247 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2022-03-09

No results posted yet for this study

Summary

The main purpose of the study is to examine whether operating room (OR) efficiency will be improved by significantly decreasing non operative time. This study also aims: 1) to evaluate whether a decrease in non-operative time will result in increased surgeon and staff satisfaction, 2) to determine whether there is an increase in the complication rate during the redesigned process perioperatively and until discharge from the post anesthesia care unit, and 3) to rate patient satisfaction.

Conditions

  • Non-operative Time
  • General Surgery, Above 18 Years of Age

Interventions

PROCEDURE

Patients will be inducted in the induction room

The patients will be inducted in the induction room

PROCEDURE

Redesigned process

The registered nurse will call in the house keeper to start cleaning of the OR (parallel processing) before the patient exits the room

DRUG

patient will be reversed with sugammadex 4mg/kg IV

The patient will be reversed with sugammadex 4mg/kg IV, and then extubated before being moved out of the OR

PROCEDURE

STANDARD PROCESS

standard process

Sponsors & Collaborators

Principal Investigators

  • Roland Kaddoum, MD · American University of Beirut Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-05-18
Primary Completion
2020-10-30
Completion
2020-10-30

Countries

  • Lebanon

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01937247 on ClinicalTrials.gov