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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05476666
Other study ID # ERC/2022/ANS/1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2022
Est. completion date June 15, 2022

Study information

Verified date August 2022
Source Pakistan Navy Station Shifa Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study is aimed at comparing peripherial venous pressure as an indicator of central venous pressure in post operative surgical patients.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date June 15, 2022
Est. primary completion date May 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - ASA I/II/III surgical patients who require central venous access as part of their surgical treatment plan with no organ support in post operative period. - Age between 18 and 75 years - Who have atleast 1 x 18 gauge peripherial venous cannula in the upper limb from elbow below to the hand - Who have given consent Exclusion Criteria: - Not meeting the inclusion criteria

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Peripherial and central venous access
Passing a peripherial and a central venous catheter/cannula

Locations

Country Name City State
Pakistan PNS Shifa Hospital Karachi Sind

Sponsors (1)

Lead Sponsor Collaborator
Pakistan Navy Station Shifa Hospital

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Peripherial venous pressure as an indicator of central venous pressure 3 months
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