NCT03846622

Brief Summary

Seven different scoring systems used for prediction of perioperative bleeding were compared regarding patients operated for elective open cardiac surgery in the investigator's study.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
500

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2016

Typical duration for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2016

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2018

Completed
13 days until next milestone

First Submitted

Initial submission to the registry

January 13, 2019

Completed
1 month until next milestone

First Posted

Study publicly available on registry

February 19, 2019

Completed
Last Updated

February 19, 2019

Status Verified

February 1, 2019

Enrollment Period

3 years

First QC Date

January 13, 2019

Last Update Submit

February 17, 2019

Conditions

Bleeding

Outcome Measures

Primary Outcomes (2)

  • Bleeding scores

    Bleeding scores were calculated in points ranging from 0 to 4.(0 the lowest and 4 the highest risk score for bleeding)

    Bleeding risk scores were calculated through study completion, an average of 2 years.

  • The amount of blood transfusions

    The amount of blood transfusions were recorded in units.

    The amount of blood transfusions were recorded through study completion, an average of 2 years.

Interventions

Calculation of scoring systems for bleedingOTHER

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients over 18 years of age who were operated for elective open cardiac surgery.

You may qualify if:

  • Patients with 18 years of age or older,
  • Patients operated for elective open cardiac surgery.

You may not qualify if:

  • Patients with incomplete data,
  • Patients with an age less than 18 years,
  • Patients operated for emergent surgical procedures.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Hemorrhage

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Tolga Saracoglu

    Associate professor of the department of anaesthesiology and reanimation

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

January 13, 2019

First Posted

February 19, 2019

Study Start

January 1, 2016

Primary Completion

December 31, 2018

Study Completion

December 31, 2018

Last Updated

February 19, 2019

Record last verified: 2019-02

Data Sharing

IPD Sharing
Will not share