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CompletedNCT06032962Updated Sep 13, 2023

Opportunistic Salpingectomy in Non-gynecological Surgeries

An interventional study of salpingectomy in Ovarian Cancer Prevention, sponsored by Dana Josephy. Completed at 1 site in Israel. Open to female participants aged 40 Years and older. Per ClinicalTrials.gov, last updated 2023-09-13.

Sponsored by Dana Josephy · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 5 years 6 months after the study started (first participant enrolled Jan 2018, registered Jul 2023).
Phase
Not applicable
Study type
Interventional
Enrollment
42
Allocation
Non-randomized
Ages
40 Years and older
Sex
Female
01

Study summary

The goal of this study is to evaluate patient's compliance for opportunistic salpingectomy (OS) and procedure feasibility in non gynecological abdominal surgeries

Read the detailed description

Patients who are candidate for non-gynecological abdominal surgery, are offered OS. If agree, a general surgeon perform the procedure during the planned abdominal surgery

02

Conditions studied

  • Ovarian Cancer Prevention
03

In context

Lead sponsor

This is the only study on the registry with Dana Josephy as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Women who were candidates for non-gynecological abdominal surgery
  • Aged 45 or older, or aged 40 or older with a desire for bilateral salpingectomy

Exclusion criteria

Exclusion Criteria:

  • Pregnant women
  • Candidates for urgent surgery
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
42 participants (actual)

Study arms

  • Experimental
    non-gynecologic surgery

    Female candidates for non-gynecologic abdominal surgery

    Procedure: salpingectomy

Interventions

  • Proceduresalpingectomy

    surgical removal of the fallopian tubes

06

What researchers measure

Primary outcomes

  1. patients willing for salpingectomy

    The number of patients that will agree for salpingectomy

    Time frame: day of enrollment

  2. patients undergoing salpingectomy

    The number of patients that will undergo salpingectomy

    Time frame: from enrollment and up to 6 weeks

  3. length of salpingectomy

    the length (in minutes) of salpingectomy

    Time frame: within surgery

  4. surgical complications

    complications during or after salpingectomy

    Time frame: up to 30 days from surgery

07

Study locations

1 site
  • Meir medical center
    Kfar Saba, Israel
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 13, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06032962
Lead sponsor
Dana Josephy
Responsible party
Dana Josephy (Dana Josephy, Meir Medical Center) — Sponsor-investigator
First posted
Sep 13, 2023
Start date
Jan 1, 2018
Primary completion
Dec 31, 2022
Completion
Feb 28, 2023
Last update
Sep 13, 2023

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2023. You cannot join it, but the record below documents what was studied.

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