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UnknownNCT03967457

Comprehensive Study on the Quality of Life in Cervical Cancer Patients

Comprehensive Study on the Quality of Life in Cervical Cancer Patients: A Prospective Cohort Study

Status
Unknown
Phase
Study type
Observational
Enrollment
10,000 (estimated)
Sponsor
Lei Li · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTquestionnaires surveyIncluding four kinds of questionnaires: European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30 (V3); EORTC QLQ-CX24; Eligibility Criteria (FSFI); and Short forms of two condition-specific quality-of-life questionnaires for women with pelvic floor disorders (PFIQ-7)
DIAGNOSTIC_TESTUrodynamic testingUrodynamic testing consists of important urodynamic parameters including: Bladder capacity at the first void sense Bladder capacity at normal desire to void Bladder capacity at strong desire to void Qmax Qave Pves at Qmax Pdet at Qmax Cves at SDV Cdet at SDV Residual urine volume
DIAGNOSTIC_TESTRectum dynamics testingRectum dynamics testing consists of important parameters of rectum activities
DIAGNOSTIC_TESTovarian reserve functionTesting for ovarian reserve function consists of: Follicle-stimulating hormone Estradiol Anti-mullerian hormone Inhibin B

Timeline

Start date
2019-06-19
Primary completion
2022-06-01
Completion
2023-06-01
First posted
2019-05-30
Last updated
2019-06-20

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03967457. Inclusion in this directory is not an endorsement.