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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01160185
Other study ID # 114015
Secondary ID
Status Completed
Phase N/A
First received July 8, 2010
Last updated July 8, 2010
Start date June 2009
Est. completion date July 2009

Study information

Verified date July 2010
Source GlaxoSmithKline
Contact n/a
Is FDA regulated No
Health authority United Kingdom: Medicines and Healthcare Products Regulatory Agency
Study type Observational

Clinical Trial Summary

This meta-analysis was conducted to investigate the efficacy of Topotecan and other treatments for recurrent and stage IVB carcinoma of the cervix


Description:

Studies included in the meta-analysis were: GOG-0179, GOG-0204 & GOG-0169


Recruitment information / eligibility

Status Completed
Enrollment 1
Est. completion date July 2009
Est. primary completion date July 2009
Accepts healthy volunteers No
Gender Female
Age group 21 Years and older
Eligibility Inclusion Criteria:

- Randomised Clinical Trials or systematic reviews or meta-analyses

- Treatment with topotecan or platinum-based single and combination regimens in female patients of any race with cancer of the cervix recurrent after radiotherapy or stage IVB disease

Exclusion Criteria:

Study Design

Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Drug:
paclitaxel
paclitacel
cisplatin
cisplatin monotherapy
topotecan
topotecan

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
GlaxoSmithKline

Outcome

Type Measure Description Time frame Safety issue
Primary Survival 12 months
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