Clinical Trials Directory

Trials / Terminated

TerminatedNCT01461772

Efficacy and Safety Study of Concurrent Chemoradiation Therapy to Treat Locally Advanced Cervical Cancer

Comparison of Concurrent Chemoradiation Therapy With Weekly Cisplatin and Concurrent Chemoradiation Therapy With Weekly Carboplatin in Locally Advanced Cervical Cancer: Phase III Multicenter Prospective Randomized Controlled Trial

Status
Terminated
Phase
Phase 3
Study type
Interventional
Enrollment
21 (actual)
Sponsor
Asan Medical Center · Academic / Other
Sex
Female
Age
20 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Concurrent chemoradiation therapy with weekly cisplatin is the current standard treatment for patients with locally advanced cervical cancer. However, weekly cisplatin is related to renal toxicity and not convenient regimen. Recently, carboplatin has proved to be a good radiosensitizer and less renal toxicity. Weekly carboplatin is more convenient regimen for both patients and physicians. Weekly carboplatin may have similar efficacy with weekly cisplatin and may have more favorable toxicity profile. Therefore, the investigators aimed to evaluate the efficacy and safety of concurrent chemoradiation with weekly carboplatin in patients with locally advanced cervical cancer.

Conditions

Interventions

TypeNameDescription
RADIATIONRadiation therapypelvic radiation therapy (Extended filed radiation therapy and addition of brachytherapy is allowed)
DRUGCarboplatincarboplatin 130mg/m2BSA on day 1,8,15,22,29,and 36
DRUGCisplatinCisplatin 40mg/m2BSA on day 1,8,15,22,29,and 36

Timeline

Start date
2009-12-01
Primary completion
2014-05-01
Completion
2014-05-01
First posted
2011-10-28
Last updated
2017-05-31

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01461772. Inclusion in this directory is not an endorsement.