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Evaluation of Surgical Complications

NCT ID: NCT01168193

Last Updated: 2013-09-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

2200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-01-31

Brief Summary

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Surgical complications may be very serious and are often under-reported. The aim of this study it to document and study all the postoperative complications at our department during one year using a novel grading system.

Detailed Description

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Conditions

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Post Operative Complications

Keywords

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surgery post operative complications length of stay

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Blinding Strategy

NONE

Study Groups

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Patients that underwent surgery

Single arm

Group Type OTHER

No intervention

Intervention Type OTHER

Interventions

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No intervention

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* All patients undergoing surgery at our department.
* No gender difference.

Exclusion Criteria

* Age - less than 18.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hadassah Medical Organization

OTHER

Sponsor Role lead

Responsible Party

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Hagai Mazeh

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Haggi Mazeh, MD

Role: PRINCIPAL_INVESTIGATOR

Hadassah Medical Organization

Other Identifiers

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Complications-HMO-CTIL

Identifier Type: -

Identifier Source: org_study_id