Efficiency of Patient Blood Management Protocol in Gynecological Surgery Department (PERIOPESGYNECO)

NCT ID: NCT06493435

Last Updated: 2024-07-10

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

NOT_YET_RECRUITING

Total Enrollment

160 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-06-30

Study Completion Date

2026-12-31

Brief Summary

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Perioperative anemia is associated with higher risk of red blood cell transfusion, higher rates of morbimortality and lower quality of postoperative recovery. In a context of focussing on higher quality management and improved recovery after surgery, development of Patient Blood management has increased. This study aim to assess PBM protocole in a postoperative context of gynaecological surgery, by comparing indicators at two time periods: 2 and 8 months after establishment of PBM protocol.

Detailed Description

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Conditions

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Anemia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* age \> 18 years
* being hospitalised for planned hysterectomy or cancer related ovariectomy

Exclusion Criteria

* less than 18 years
* non french speaker
* being under a legal individual protection measure
* not being able to consent
* being opposed to data collection
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Angers

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Sigismond Lasocki

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Angers

Central Contacts

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Sigismond Lasocki

Role: CONTACT

0241353635 ext. +33

Elise Houssin

Role: CONTACT

02 41 35 36 37 ext. +33

Other Identifiers

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24_0207

Identifier Type: -

Identifier Source: org_study_id

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