Living With Cervical Cancer: Assessing Utilities Associated With Common Treatment Complications
NCT ID: NCT01039493
Last Updated: 2015-10-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
40 participants
OBSERVATIONAL
2010-02-28
2010-08-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Discovering Factors in Cervical Cancer Patients' Clinical Trial Experiences
NCT05789628
Development & Validation of Utilities for Health States Relevant to Cervical Cancer Patients
NCT00788216
Patient Satisfaction & Quality Of Life in Patients With Cervical Cancer
NCT00473798
Laparoscopic Sentinel Lymph Node Localization in Operable Cervix Cancer
NCT00205010
Sexual Functioning in Cervical Cancer Survivors
NCT00522223
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Patients
No interventions assigned to this group
Providers
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Subjects must be ≥18 and \<61 years old.
Exclusion Criteria
* Subjects who do not have capacity to consent will not be included in this study.
* Subjects may not be investigators on this study.
18 Years
61 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Wisconsin, Madison
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Ellen M Hartenbach, MD
Role: PRINCIPAL_INVESTIGATOR
University of Wisconsin, Madison
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University of Wisconsin-Madison
Madison, Wisconsin, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
OS09708
Identifier Type: OTHER
Identifier Source: secondary_id
M-2009-1240
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.