Comprehensive Study on the Quality of Life in Cervical Cancer Patients

  • STATUS
    Recruiting
  • End date
    Jun 1, 2023
  • participants needed
    10000
  • sponsor
    Lei Li
Updated on 23 January 2021
cancer
hysterectomy
carcinoma
diagnostic procedures
carcinomas
radical hysterectomy

Summary

This is prospective cohort study. All the patients with primary cervical cancer in the future three years in Peking Union Medical College Hospital will be included in this study. Before and after the major therapy (including at least radical hysterectomy and/or radiotherapy), the patients accept (1) the questionnaires survey about quality of life; (2) urodynamic testing; (3) rectum dynamics testing and (4) ovarian reserve function. The survival outcomes (disease-free survival and overall survival) will be supplemented as secondary objectives.

Details
Condition Disease-Free Survival, Cervical Cancer, Cervical Cancer, Survival Rate, Disorders of cervix NOS, Uterine Cancer, Uterine Cancer, Urodynamics, Survival, Quality of life, Pregnancy Complications, Pregnancy Complications, Sexual Dysfunction, Pelvic Floor Disorders, Ovarian Reserve Function, Overall Survival, Rectum Dynamics, Sex Dysfunction, cervical carcinoma, urodynamic studies, sexual disorders, cervical cancer, uterine, quality-of-life, carcinoma of the cervix uteri, carcinoma of the cervix, cervix cancer, cancer of the cervix, carcinoma of cervix
Treatment questionnaires survey, Urodynamic testing, Rectum dynamics testing, ovarian reserve function, ovarian reserve function
Clinical Study IdentifierNCT03967457
SponsorLei Li
Last Modified on23 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Not accepting any of the four kinds of evaluations for quality of life
Recurrent patients
Not achieving response after above major therapy
Clear my responses

How to participate?

Step 1 Connect with a study center
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

Primary Contact

site

0/250

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

Learn more

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

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...

Browse trials for

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

user name

Added 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 annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note