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Hysterectomy with TUbectomy (HYSTUB) study

Hysterectomy with TUbectomy (HYSTUB) study - HYSTUB

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON40051
Enrollment
110
Registered
2012-08-21
Start date
2013-06-28
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

premature ovarian Faillure

Interventions

One group will undergo a regular hysterectomy only (either vaginal, abdominal or laparoscopically) (=control group). The other group will receive a regular hysterectomy including a bilateral salping

Sponsors

TweeSteden ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Otherwise healthy women undergoing hysterectomy for benign indications (eg. bleeding disorder, fibroids, adenomyosis) without a family history of ovarian / tubal / breast cancer, will be asked to participate.

Exclusion criteria

Exclusion criteria: Family history of cancer, history of any form of cancer

Design outcomes

Primary

MeasureTime frame
concentration AMH, FSH and oestradiol pre- and six months postoperatively. Does a salpingectomy during hysterectomy for benign indications change hormonal status significantly, indicating a shift towards menopausal status?

Secondary

MeasureTime frame
What is the incidence of premalignancies in Fallopian tubes from women not at hereditary high risk to develop serous carcinomas? Is there a difference in quality of life (QoL) between the two groups?

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)