NCT06522009

Brief Summary

To detect the effect of time delay and syringe surface area on the oxygen tension (PaO2), oxyhaemoglobin saturation (SaO2), acidity (pH), and carbon dioxide tension (PaCO2) in both arterial and venous blood gas outcomes.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
45

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jul 2019

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

July 30, 2019

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 30, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 30, 2020

Completed
4 years until next milestone

First Submitted

Initial submission to the registry

July 18, 2024

Completed
8 days until next milestone

First Posted

Study publicly available on registry

July 26, 2024

Completed
Last Updated

August 9, 2024

Status Verified

August 1, 2024

Enrollment Period

1 year

First QC Date

July 18, 2024

Last Update Submit

August 7, 2024

Conditions

Keywords

blood gasoxygen saturationsyringe surface areaTime Delay

Outcome Measures

Primary Outcomes (1)

  • To detect the effect of time delay and syringe surface area on the oxygen tension (PaO2) arterial and venous blood gas outcomes.

    PaO2 by mmhg arterial and venous samples To detect the effect of time delay and syringe surface area on SO2 in arterial and venous samples To detect the effect of time delay and syringe surface area on other parameters of blood gases e.g. PH,CO2

    1 hour

Secondary Outcomes (1)

  • effect of delay on analysis oxyhaemoglobin saturation (SaO2) acidity (pH) carbon dioxide tension (PaCO2)

    60 minutes

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Critically ill-patients, and intraoperative patients who aged above 18 years.

You may qualify if:

  • Critically ill-patients, and intraoperative patients who aged above 18 years.

You may not qualify if:

  • Patients with haematological diseases e.g. sickle cell anaemia
  • burn patients with risk of carbon monoxide poisoning
  • ARDS
  • pulmonary oedema
  • samples that were clotted

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Theodor Bilharz Research Institute

Cairo, 3357, Egypt

Location

MeSH Terms

Conditions

Respiratory Insufficiency

Condition Hierarchy (Ancestors)

Respiration DisordersRespiratory Tract Diseases

Study Officials

  • Adel A hassan, Md

    Helwan University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
lecturer of anaesthesia, intensive care and pain management

Study Record Dates

First Submitted

July 18, 2024

First Posted

July 26, 2024

Study Start

July 30, 2019

Primary Completion

July 30, 2020

Study Completion

July 30, 2020

Last Updated

August 9, 2024

Record last verified: 2024-08

Data Sharing

IPD Sharing
Will share

The data will be available upon a reasonable request from the corresponding author after the end of study for one year.

Shared Documents
STUDY PROTOCOL
Time Frame
after the end of the study for one year
Access Criteria
The data will be available upon a reasonable request from the corresponding author.

Locations