The Effect of Postoperative Therapy on the Quality of Life of Patients With Early Cervical Cancer Research

NCT ID: NCT02018003

Last Updated: 2013-12-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

180 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-01-31

Study Completion Date

2016-12-31

Brief Summary

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The purpose of this study is to assess the women's quality of life, who accepted chemotherapy,radiotherapy, concurrent radiochemotherapy or who didn't accept therapy, after operation.

Detailed Description

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The study projects to follow up 180-200 early stage cervical cancer patients after operation and assess the women's quality of life by the scales: ECOG, Functional Assessment of Cancer Therapy, EuroQol-5 Dimensions, and Kupperman index.

Conditions

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Uterine Cervical Neoplasms

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* ≮ 18 years, cervical cancer verified by pathology,

* IIA stage, accepted the operation ( Piver III and pelvic lymph node dissection) as initial therapy, obtained the patient's agreement

Exclusion Criteria

* the patient had accepted chemotherapy or radiotherapy before operation
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Peking University

OTHER

Sponsor Role lead

Responsible Party

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Yunong Gao

the head of department of gynecological oncology

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Gao Yunong

Role: STUDY_DIRECTOR

Peking University

Central Contacts

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Gao Weijiao

Role: CONTACT

Phone: 86-10-88196102

Email: [email protected]

Other Identifiers

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PUCRP201309

Identifier Type: -

Identifier Source: org_study_id