NCT01707511

Brief Summary

Et-C02 is used to predict PaCO2 during surgery. There are controversies regarding the value of ETCO2 to predict PaCO2. The aim of this study was to investigate the relation between Et-CO₂ and PaCO₂ measurements in patients undergoing laparoscopic colorectal surgery. Patient and surgical characteristics, mechanical ventilation adjustments, and intraabdominal pressure values and the corelation between these parameters and EtCO₂ - PaCO₂ difference were also investigated.

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
40

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jan 2012

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

January 1, 2012

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2012

Completed
7 months until next milestone

First Submitted

Initial submission to the registry

September 15, 2012

Completed
1 month until next milestone

First Posted

Study publicly available on registry

October 16, 2012

Completed
1.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2013

Completed
Last Updated

October 16, 2012

Status Verified

October 1, 2012

Enrollment Period

2 months

First QC Date

September 15, 2012

Last Update Submit

October 15, 2012

Conditions

Keywords

Arterial carbondioxide pressureColon surgeryEnd-tidal carbondioxideLaparoscopic Trendelenburg

Eligibility Criteria

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

Patients scheduled whom planned for elective laparoscopic colorectal resection.

You may qualify if:

  • ASA I-III patients underwent laparoscopic colorectal resection

You may not qualify if:

  • convertion to the open surgery

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Diskapi Teaching and Research Hospital

Ankara, Altindag, 06110, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Colorectal Neoplasms

Condition Hierarchy (Ancestors)

Intestinal NeoplasmsGastrointestinal NeoplasmsDigestive System NeoplasmsNeoplasms by SiteNeoplasmsDigestive System DiseasesGastrointestinal DiseasesColonic DiseasesIntestinal DiseasesRectal Diseases

Study Officials

  • Mustafa Ozmen, MD

    Diskapi Yildirim Beyazit Education and Research Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principal İnvestigator

Study Record Dates

First Submitted

September 15, 2012

First Posted

October 16, 2012

Study Start

January 1, 2012

Primary Completion

March 1, 2012

Study Completion

December 1, 2013

Last Updated

October 16, 2012

Record last verified: 2012-10

Locations