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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01589406
Other study ID # 538-10CTIL
Secondary ID
Status Not yet recruiting
Phase N/A
First received April 29, 2012
Last updated May 1, 2012
Start date June 2012
Est. completion date May 2014

Study information

Verified date April 2012
Source Rambam Health Care Campus
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

Patients with premalignant (CIN3) and malignant cervical cancer will asked to complete questionnaires regarding intimacy (ENRICH) and life adaptation (PAIS) before treatment (surgery or radiotherapy) and after completion of treatment in order to estimate the influence of disease and treatment on quality of life indices.


Description:

no additional information. see above


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date May 2014
Est. primary completion date May 2014
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- women with Gynaecological cancer intended to undergo chemotherapy or surgery

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Rambam Medical Center Haifa

Sponsors (1)

Lead Sponsor Collaborator
Rambam Health Care Campus

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of life longitudinal describtion of quality of life during treatment 2 years No
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