Opportunistic Salpingectomy in Non-gynecological Surgeries
1 other identifier
interventional
42
1 country
1
Brief Summary
The goal of this study is to evaluate patient's compliance for opportunistic salpingectomy (OS) and procedure feasibility in non gynecological abdominal surgeries
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2018
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
February 28, 2023
CompletedFirst Submitted
Initial submission to the registry
July 19, 2023
CompletedFirst Posted
Study publicly available on registry
September 13, 2023
CompletedSeptember 13, 2023
September 1, 2023
5 years
July 19, 2023
September 4, 2023
Conditions
Outcome Measures
Primary Outcomes (4)
patients willing for salpingectomy
The number of patients that will agree for salpingectomy
day of enrollment
patients undergoing salpingectomy
The number of patients that will undergo salpingectomy
from enrollment and up to 6 weeks
length of salpingectomy
the length (in minutes) of salpingectomy
within surgery
surgical complications
complications during or after salpingectomy
up to 30 days from surgery
Study Arms (1)
non-gynecologic surgery
EXPERIMENTALFemale candidates for non-gynecologic abdominal surgery
Interventions
Eligibility Criteria
You may qualify if:
- Women who were candidates for non-gynecological abdominal surgery
- Aged 45 or older, or aged 40 or older with a desire for bilateral salpingectomy
You may not qualify if:
- Pregnant women
- Candidates for urgent surgery
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Dana Josephylead
Study Sites (1)
Meir medical center
Kfar Saba, Israel
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Dana Josephy
Study Record Dates
First Submitted
July 19, 2023
First Posted
September 13, 2023
Study Start
January 1, 2018
Primary Completion
December 31, 2022
Study Completion
February 28, 2023
Last Updated
September 13, 2023
Record last verified: 2023-09