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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03838705
Other study ID # SS1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 20, 2018
Est. completion date July 1, 2018

Study information

Verified date February 2019
Source Umraniye Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In our study, we aimed to investigate the relationship between STOP-BANG and 4-Variable Screening questionnaires in postoperative period in patients who underwent bariatric surgery.


Recruitment information / eligibility

Status Completed
Enrollment 87
Est. completion date July 1, 2018
Est. primary completion date June 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 64 Years
Eligibility Inclusion Criteria:

- BMI>40

- bariatric surgery patients

Exclusion Criteria:

- malignancy

- patients who are unable to complete the questionnaire

- patients who needs laparotomy

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
hypoxia
It was accepted that hypoxia developed in patients with SpO2< 92 or falling over 20% compared to preoperative values.
normooxy
It was accepted that patients with SpO2 between 100-92 mmHg

Locations

Country Name City State
Turkey Istanbul Umraniye Training Hospital Istanbul

Sponsors (3)

Lead Sponsor Collaborator
Umraniye Education and Research Hospital Aysun Isiklar, Sibel Ocak Serin

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary SpO2 Peripheral Oxygen Saturation 48 hours
Secondary STOP-BANG The value of STOP-BANG questionnaire preoperative 24 hours
Secondary 4-V Tool The value of 4-V Tool preoperative 24 hours
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