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NCT01160185 Clinical Trial

Meta-analysis of Efficacy of Topotecan

Cervical Intraepithelial Neoplasia Clinical Trial

Official title:
Meta-analysis of Efficacy of Topotecan and Other Treatments for Recurrent Carcinoma of the Cervix

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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