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Retrospective Analysis of the Incidence of Complications From Transvaginal Oocyte Retrieval (TVOR).

Retrospective Analysis of the Incidence of Complications From Transvaginal Oocyte Retrieval (TVOR).

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03282279
Acronym
TVOR
Enrollment
23827
Registered
2017-09-13
Start date
1996-06-23
Completion date
2017-09-30
Last updated
2019-03-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

In Vitro Fertilization

Keywords

oocyte retrieval, surgical complications

Brief summary

The investigators retrospectively analysed the complication rate of ultrasound guided transvaginal oocyte retrieval (TVOR) from all the procedures performed between 1996 and October 2016 in a tertiary level university based fertility clinic.

Detailed description

Ultrasound guided transvaginal oocyte retrieval (TVOR) is nowadays gold standard techniques to collect oocyte after ovulation induction in Assisted Reproductive techniques (ART). It is a very safe technique with infectious complications of any kind occurring in just 1% (Bennett et al.) of all procedures, vaginal bleeding in 0 to 1.3% of the procedures (Ludwig et al., Bodri et al., Aragona et al.) and vascular, gastrointestinal and genitourinary (Grynberg et al. and Catanzarite and al.), injuries being extremely rare (Bennett et al.). Case reports account also for rarer complications such as ovarian abscess formation (Kelada & Ghan and Sharp et al.) pseudoanerysm formation (Bozdag et al. and Jayakrishnan et al.), uroretroperitoneum (Fiori et al.). The rational of thestudy is to provide the percentages of complication from TVOR of the Fertility Center of Humanitas Research Hospital, also considering the development in time of technologies and techniques in Assisted Reproduction. Another rational is inquire whether there is any risk factor for such complications in order to try to prevent them in future procedures. The investigators performed a retrospective observational study including all the transvaginal oocyte retrieval procedures performed between 1996 and October 2016. The data have been collected from the Humanitas Fertility Center' Department database (ART.it). Because of the retrospective nature of this study, a specific informed consent was not necessary.

Interventions

PROCEDURETVOR

Ultrasound guided transvaginal oocyte retrieval (TVOR) in deep sedation for IVF.

Sponsors

Istituto Clinico Humanitas
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 46 Years
Healthy volunteers
No

Inclusion criteria

* patients that underwent ultrasound guided transvaginal oocyte retrieval during the study period

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frameDescription
complications rate20 yearsnumber of oocyte retrieval complications reported / number of procedures

Secondary

MeasureTime frameDescription
hospitalisation rate20 yearsnumber of oocyte retrieval complications reported that required a admission to the hospital/ number of procedures

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026