Evaluation of the Predictive Nature of the Postoperative CRP on Postoperative Recovery in Patients Undergoing Colorectal Resection (CRP-Track)

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

176 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-07-06

Study Completion Date

2017-06-13

Brief Summary

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Colic and rectal resection represents a majority of hospitalizations in visceral surgery. The objective of this study was to evaluate the prognostic of inflammatory markers dosage (CRP, procalcitonin and venous lactate) on the postoperative recovery after colorectal surgery and on the length of stay.

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Detailed Description

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Conditions

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Colorectal Postoperative Complication

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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C-reactive protein dosage

Group Type EXPERIMENTAL

C-reactive protein dosage

Intervention Type OTHER

Interventions

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C-reactive protein dosage

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Upper age to 18 years
* Planned hospital stay for a colonic resection with anastomosis without permanent or temporary digestive bypass
* Patient with pre-operative CRP lower or egal to 172 mg/L
* No opposition at the participation of the study
* Expected patient return home after surgery (or convalescent home or not medicalized institution)

Exclusion Criteria

* Patient under guardianship
* Protected or private patient freedom
* Minor patient
* Colectomy surgery with digestive bypass or digestive anastomosis
* Complex combined surgery (significantly intestinal resection associated, another surgical procedure that can interfere with postoperative CRP)
* General inflammatory disease susceptive to modify dosage values
* Anti-inflammatory therapy (AINS/ corticosteroids/ immunosuppressive)
* Patient unable to understand the study

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No