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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03144310
Other study ID # NK/3067/MD/320
Secondary ID
Status Completed
Phase N/A
First received May 4, 2017
Last updated December 29, 2017
Start date November 1, 2016
Est. completion date November 2017

Study information

Verified date December 2017
Source Postgraduate Institute of Medical Education and Research
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Pre op ultrasound with chest auscultation and arterial blood gas, after extubation ultrasound with chest auscultation and blood gas, 12hrs chest auscultation with ultasaound, 24 hrs chest auscultation and ultrasound to see atelectasis


Description:

Pre op ultrasound with chest auscultation and arterial blood gas, after extubation ultrasound with chest auscultation and blood gas, 12hrs chest auscultation with ultasaound, 24 hrs chest auscultation and ultrasound to see atelectasis inclusion criteria: age 18 to 70 yrs age ASA I and II robot assisted pelvic surgeries in steep trendelenburg position

exclusion criteria: cardiac disese severe obstructive and restrictive disease upper airways infection ASAIII and IV


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date November 2017
Est. primary completion date November 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- ASA Iand II age 18-70 yrs robot assisted pelvis surgeries

Exclusion Criteria:

- ASA II and IV cardiac and lung disease

Study Design


Related Conditions & MeSH terms


Intervention

Other:
lung ultrasound
lung ultrasound and blood gas

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Postgraduate Institute of Medical Education and Research

Outcome

Type Measure Description Time frame Safety issue
Primary incidence of atelectasis incidence of atelectasis in adults after extubation undergoing robot assisted pelvic laproscopic surgery in steep trendelenberg position using ultrasound 24hrs
Secondary risk factor identification risk factor identification of post operative atelectasis 24hrs