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Optical Biopsy and Fallopian Tube

Dynamic Real-time in Vivo Confocal Laser Endomicroscopy Cellvizio® of the Fallopian Tube During Laparoscopy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02365779
Acronym
FALLOPTIC
Enrollment
40
Registered
2015-02-19
Start date
2015-01-31
Completion date
2015-08-31
Last updated
2025-09-11

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

Conditions

Bilateral Laparoscopic Salpingectomy

Keywords

salpingectomy, optical biopsy, Cellvizio®

Brief summary

High-grade serous ovarian cancer is the most threatening type of gynaecological cancer with an important mortality due to late diagnosis. However the prognosis is excellent in the early stages of the disease. Recently it has been described a new serous carcinogenic sequence from the fallopian tube with tubal precancerous lesions. Therefore the identification of these early preinvasive lesions would be of great interest in the population with hereditary predisposition for ovarian cancer (concept of oncofertility) and in the general population (to determine whether bilateral salpingectomy has to be performed during a hysterectomy for benign disease). The optical biopsy has been developed and validated in the detection of early precancerous lesions (such as Barrett's oesophagus or in situ cancer of the bladder). The first objective of this study is to prospectively assess the efficacy of optical biopsy (Cellvizio®) in the study of fallopian tubes during laparoscopy with correlation between the histopathological and immunohistochemical analysis and the endomicroscopy image interpretation. The second objective is to describe the optical biopsy pictures in order to state a classification.

Detailed description

Inclusion Criteria: * Woman aged 18 years or more * All patients with laparoscopic salpingectomy for benign conditions (tubal ligation, during a hysterectomy), for prophylactic conditions (BRCA mutation) or in case of pelvic cancers * Informed and signed consent Exclusion Criteria: * Interview revealing disorder entailing unacceptable risk of postoperative complications: coagulation disorder, immune system disorder, evolutive disease, etc. * Pregnancy, ongoing or planned during the study period * Allergy to fluorescein * Previous allergy or anaphylactic shock during an angiography * Allergic or hypersensibility reactions * Severe asthma, chronic cardiac or pulmonary diseases * Restricted renal function * Patient under a beta-blockers treatment * Inability to understand information provided * Not covered by a national health insurance scheme, prisoner or under administrative supervision

Interventions

PROCEDUREbilateral laparoscopic salpingectomy

Use of the confocal laser endomicroscopy Cellvizio® system during laparoscopy salpingectomy

DEVICEendomicroscopy Cellvizio® system

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

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

Inclusion criteria

* Woman aged 18 years or more * All patients with laparoscopic salpingectomy for benign conditions (tubal ligation, during a hysterectomy), for prophylactic conditions (BRCA mutation) or in case of pelvic cancers * Informed and signed consent

Exclusion criteria

* Interview revealing disorder entailing unacceptable risk of postoperative complications: coagulation disorder, immune system disorder, evolutive disease, etc. * Pregnancy, ongoing or planned during the study period * Allergy to fluorescein * Previous allergy or anaphylactic shock during an angiography * Allergic or hypersensibility reactions * Severe asthma, chronic cardiac or pulmonary diseases * Restricted renal function * Patient under a beta-blockers treatment * Inability to understand information provided * Not covered by a national health insurance scheme, prisoner or under administrative supervision

Design outcomes

Primary

MeasureTime frame
Correlation between the histopathological and immunohistochemical analysis and the endomicroscopy image interpretationDAY 1

Secondary

MeasureTime frame
: Description of the optical biopsy pictures in order to state a classificationDAY 1

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026