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Clinical Trials/NCT05895227
NCT05895227CompletedNot Applicable

Hemorrhagic Complications of Transvaginal Oocyte's Retrieval: an Update.

Istituto Clinico Humanitas0 sites13,193 target enrollmentStarted: January 1, 2017Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
13,193
Primary Endpoint
Hemoperitoneum after oocyte transvaginal retrieval

Study Overview

Brief Summary

The goal of this retrospective analysis is to focus on peritoneal bleeding after oocyte retrieval and to further investigate factors related to this specific complication and if hemorrhagic complication rate modifications can be observed.

Detailed Description

The main aim is to update our knowledge on oocyte retrieval complication, focusing specifically on hemorrhagic / hemoperitoneum rate.

All retrievals will be retrieved in IVF/ICSI cycles and Fertility Preservation both in oncological patients and in patients requesting oocyte storage for deferring motherhood.

Data collection goes from January 2017 to December 2022.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •patients that underwent a procedure of oocyte transvaginal retrieval for IVF/ intracytoplasmatic sperm injection (ICSI) cycles and fertility preservation

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Hemoperitoneum after oocyte transvaginal retrieval

Time Frame: Oocyte retrievals in the period January 2017- December 2022

number of patients with onset of hemoperitoneum

Secondary Outcomes

  • Operator of the procedure(6 years)
  • Time of symptoms onset(6 years)
  • Loss of blood during procedure(6 years)
  • Need for hospitalization(6 years)
  • Incidence compared to past case history(6 years)
  • Hemoglobin level before and after procedure(6 years)

Investigators

Sponsor
Istituto Clinico Humanitas
Sponsor Class
Other
Responsible Party
Sponsor

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