Adjuvant Chemotherapy for Locally Advanced Cervical Cancer

NCT02036164 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 500

Last updated 2017-04-06

No results posted yet for this study

Summary

Data of survival benefit from adjuvant chemotherapy (ACT) after concurrent chemoradiation (CCRT) for locally advanced cervical cancer (LACC) are still limited and inconsistent. We will investigate if ACT has survival benefit over CCRT alone.

Conditions

  • Uterine Cervical Cancer

Interventions

RADIATION

Pelvic radiation

Radiation: * Pelvic radiation 1.8 Gy/ day, 5 days/ week, 6 weeks * Brachytherapy 30-35 Gy for 4-5 times

DRUG

Cisplatin

Cisplatin 40 mg/m2 i.v.

DRUG

Paclitaxel

Paclitaxel 175 mg m2 i.v.

DRUG

Carboplatin

Carboplatin AUC 5 i.v.

Sponsors & Collaborators

  • National Research Council of Thailand

    collaborator OTHER_GOV
  • Navamindradhiraj University

    collaborator OTHER
  • Chiang Mai University

    collaborator OTHER
  • Prince of Songkla University

    collaborator OTHER
  • Bhumibol Adulyadej Hospital

    collaborator OTHER
  • Lopburi Cancer Hospital

    collaborator UNKNOWN
  • Ubonratchathani Cancer Hospital

    collaborator UNKNOWN
  • Udonthani Cancer Hospital

    collaborator UNKNOWN
  • Chonburi Cancer Hospital

    collaborator UNKNOWN
  • Lampang Cancer Hospital

    collaborator OTHER
  • Health Intervention and Technology Assessment Program

    collaborator UNKNOWN
  • Rajburi Hospital

    collaborator UNKNOWN
  • Siriwan Tangjitgamol, MD

    lead OTHER

Principal Investigators

  • Siriwan Tangjitgamol, MD · Navamindradhiraj University

  • Vichan Lordvithaya, MD · Chiang Mai University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-01-31
Primary Completion
2018-01-31
Completion
2019-01-31

Countries

  • Thailand

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02036164 on ClinicalTrials.gov