Feasibility Study of Using Molecular Fluorescence Guided Surgery in Endometriosis

  • STATUS
    Recruiting
  • participants needed
    10
  • sponsor
    University Medical Center Groningen
Updated on 8 November 2020

Summary

Incomplete resection of endometriosis lesions often results in recurrence of symptoms and the need for repeated surgery, with considerable associated morbidity. The aim of this pilot project is to determine the feasibility of fluorescence imaging to improve the treatment of endometriosis in the future.

Details
Treatment Bevacizumab-800CW
Clinical Study IdentifierNCT02975219
SponsorUniversity Medical Center Groningen
Last Modified on8 November 2020

Adding a note
adding personal notes guide

Select a piece of text and start making personal notes.

Eligibility

Yes No Not Sure

Inclusion Criteria

Is your age between 18 yrs and 99 yrs?
Gender: Male or Female
Do you have Endometriosis?
Females aged 18 years
Scheduled for surgery for the treatment of endometriosis
WHO performance score of 0-2
Written informed consent
For female subjects who are of childbearing potential, are premenopausal with
intact reproductive organs or are less than 2 years post-menopausal
\. A negative serum pregnancy test prior to receiving the tracer
\. Willing to ensure that she or her partner uses effective contraception
during the trial and for 6 months thereafter

Exclusion Criteria

Medical or psychiatric conditions that compromise the patient's ability to give informed consent
Pregnancy
History of infusion reactions to Bevacizumab or other monoclonal antibody therapies
Significant renal, cardiac, or pulmonary disease (ASA III-IV)
Clear my responses

How to participate?

Step 1 Connect with a site
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar
Name

Primary Contact

site
Name

Phone Email

0/250
Please verify that you are not a bot.
Step 2 Get screened

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more
Step 3 Enroll in the clinical study

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more
Step 4 Get your study results

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

Study

user name

Annotated by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No made yet