Evaluation of the Coagulation Profile by Thromboelastography in Bariatric Patients

Bariatric Patients Undergoing Bariatric Surgery Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01819207
• Other study ID #: 1492MF
• Status: Completed
• Phase: N/A
• First received: March 24, 2013
• Last updated: May 31, 2016
• Start date: April 2013
• Est. completion date: April 2015

Study information

• Verified date: March 2013
• Source: Western Galilee Hospital-Nahariya
• Contact: n/a
• Is FDA regulated: No
• Health authority: Israel: Ethics CommissionIsrael: Ministry of Health
• Study type: Interventional

Clinical Trial Summary

thromboelastography can identify alteration in the coagulation profile in bariatric patients who undergo sleeve gastrectomy or gastric bypass

Recruitment information / eligibility

• Status: Completed
• Enrollment: 93
• Est. completion date: April 2015
• Est. primary completion date: April 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• patients undergoing bariatric surgery

Exclusion Criteria:

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

• Bariatric Patients Undergoing Bariatric Surgery

Intervention

Other:
• blood test by thromboelastography

Locations

Country	Name	City	State
Israel	Naharia Medical Center	Naharia

Sponsors (1)

Lead Sponsor	Collaborator
Western Galilee Hospital-Nahariya

Country where clinical trial is conducted

Israel, 

References & Publications (1)

Munro TG. Glass is detectable on plain radiographs. CMAJ. 1989 Feb 15;140(4):365. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	coagulation profile by thromboelastography		1 year	No