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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02976649
Other study ID # FMASU R 19/2016
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2016
Est. completion date June 2016

Study information

Verified date July 2019
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to propose a multi-dimensional score to predict those patients undergoing bariatric surgeries who will be in need for postoperative ICU admission.


Description:

A multi-dimensional score of 7 risk factors was proposed which may help in identifying morbidly obese patients undergoing bariatric surgeries who will need admission to a critical care unit postoperatively for follow up.


Recruitment information / eligibility

Status Completed
Enrollment 111
Est. completion date June 2016
Est. primary completion date June 2016
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria:

- patients who have been operated upon for either laparoscopic gastric sleeve or laparoscopic gastric bypass during the period from January to June 2016.

Exclusion Criteria:

- Patients were excluded in case of postoperative surgical complications, conversion to open surgery or in case of redo.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Egypt Faculty of Medicine, Ain Shams University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Creation of a multi-dimensional score for the need of post-bariatric surgery ICU admission Through study completion, an average of six months.
See also
  Status Clinical Trial Phase
Completed NCT02301416 - Qsymia as an Adjunct to Surgical Therapy in the Superobese Phase 2