NCT01865019

Brief Summary

pressure controlled ventilation will improve oxygenation indices , hemodynamics during anesthesia for living donor liver transplantation recipients ,improving postoperative graft function and decreasing postoperative pulmonary complications

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Apr 2013

Geographic Reach
1 country

1 active site

Status
unknown

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

April 1, 2013

Completed
22 days until next milestone

First Submitted

Initial submission to the registry

April 23, 2013

Completed
1 month until next milestone

First Posted

Study publicly available on registry

May 30, 2013

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2014

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2014

Completed
Last Updated

May 30, 2013

Status Verified

May 1, 2013

Enrollment Period

1.5 years

First QC Date

April 23, 2013

Last Update Submit

May 26, 2013

Conditions

Outcome Measures

Primary Outcomes (1)

  • oxygen tension

    during intraoperative period

Secondary Outcomes (1)

  • decreased postoperative pulmonary complications

    one week postoperative

Other Outcomes (1)

  • improved intraoperative hemodynamics

    intraoperative

Study Arms (2)

volume controlled

volume ontrolled ventilation

Device: mechanical ventilation

pressure controlled

pressure controlled ventilation

Device: mechanical ventilation

Interventions

pressure controlledvolume controlled

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

living donor liver transplantation recipients

You may qualify if:

  • all living donor liver transplantation recipients scheduled

You may not qualify if:

  • Moderate to severe restrictive pulmonary functions

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gastroenterology center

Al Mansurah, Dakahlia Governorate, Egypt

RECRUITING

MeSH Terms

Interventions

Respiration, Artificial

Intervention Hierarchy (Ancestors)

Airway ManagementTherapeuticsResuscitationEmergency TreatmentRespiratory Therapy

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Target Duration
7 Days
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PROFESSOR

Study Record Dates

First Submitted

April 23, 2013

First Posted

May 30, 2013

Study Start

April 1, 2013

Primary Completion

October 1, 2014

Study Completion

December 1, 2014

Last Updated

May 30, 2013

Record last verified: 2013-05

Locations