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A Randomised Controlled Trial Between Two Different HDR Brachytherapy Schedule in Locally Advanced Carcinoma of Uterine Cervix

Primary Purpose

Squamous Cell Carcinoma of Cervix

Status
Completed
Phase
Phase 3
Locations
Bangladesh
Study Type
Interventional
Intervention
HDR Brachytherapy of 9 Gy in 2 fractions
HDR Brachytherapy of 7 Gy in 3 fractions
Sponsored by
Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Squamous Cell Carcinoma of Cervix focused on measuring Carcinoma cervix, RCT(randomised controlled trial), 9 Gray, Brachytherapy

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Locally advanced carcinoma cervix (stage 2b - 4a)
  • Histopathology squamous cell carcinoma

Exclusion Criteria:

  • Previous history of malignancy
  • Previously treated with radiotherapy

Sites / Locations

  • BSM Medical University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Radiation HDR Brachytherapy 9 Gy

Radiation HDR Brachytherapy 7 Gy

Arm Description

High dose rate (HDR) Brachytherapy of weekly 9 Gray in two fractions in two weeks after 50 Gray of EBRT in 2 Gray per fraction of 5 weeks with chemotherapy cisplatin 40 mg /m2 weekly for five weeks in locally advanced carcinoma cervix

High dose rate (HDR) brachytherapy of weekly 7 Gray in three fractions in three weeks after 50 Gray EBRT of 2 Gray per fraction of 25 fractions concurrently with weekly chemotherapy cisplatin40 mg /m2 in five weeks in locally advanced carcinoma cervix

Outcomes

Primary Outcome Measures

Reduction of tumor size in cervix
Comparison of pre treatment tumor size with post treatment tumor

Secondary Outcome Measures

Full Information

First Posted
May 5, 2016
Last Updated
July 13, 2018
Sponsor
Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
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1. Study Identification

Unique Protocol Identification Number
NCT02765919
Brief Title
A Randomised Controlled Trial Between Two Different HDR Brachytherapy Schedule in Locally Advanced Carcinoma of Uterine Cervix
Official Title
Study of Two Fractions Versus Three Fractions High Dose Rate Brachytherapy in Locally Advanced Carcinoma of Uterine Cervix After Pelvic Concurrent Chemoradiotherapy - a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
July 2015 (undefined)
Primary Completion Date
December 2016 (Actual)
Study Completion Date
July 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to compare two different brachytherapy treatment option in locally advanced carcinoma of uterine cervix. Brachytherapy of two fractions of 9 Gy is effective in locoregional control and more convenient in terms of cost and time than 7 Gy brachytherapy of 3 fractions in management of locally advanced carcinoma of cervix.
Detailed Description
Cervical cancer is the second most common cancer among women worldwide and is the commonest form of gynecolgic malignancy in Bangladesh.Radiotherapy in the form of external beam radiotherapy combined with intracavitary Brachytherapy is the accepted definitive mode of treatment.Limiting the number of high dose rate(HDR) Brachytherapy has the potential benefit of improving patient compliance and reducing treatment cost and duration.The aim of this study is to compare the treatment outcome and acute complications following treatment with 9 Gray (Gy) in two fractions of brachytherapy with standard EBRT in locally advanced carcinoma of cervix. EBRT will be delivered by a cobalt 60 teletherapy unit to a prescribed dose of 50 Gy in 25 fractions of 2 Gy per fraction and 5 days a week over a period of 5 weeks concurrent with inj. Cisplatin 40 mg/meter square weekly for 5 weeks.The patients will be then randomised into two arms of HDR brachytherapy,either 9Gy in 2 fractions or 7 Gy in 3 fractions.All patients will be followed up as per guideline for 6 months.The treatment related toxicity will be measured by Common Toxicity Criteria(Common terminology criteria for adverse events v.3.0). All the relevant collected data will be compiled on a master chart and then statistical analysis of the results will be obtained by using SPSS 17.The data will be analysed using Chi square test and T test.Significant value will be decided at a level of 0.05 in two tailed tests.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Squamous Cell Carcinoma of Cervix
Keywords
Carcinoma cervix, RCT(randomised controlled trial), 9 Gray, Brachytherapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Radiation HDR Brachytherapy 9 Gy
Arm Type
Experimental
Arm Description
High dose rate (HDR) Brachytherapy of weekly 9 Gray in two fractions in two weeks after 50 Gray of EBRT in 2 Gray per fraction of 5 weeks with chemotherapy cisplatin 40 mg /m2 weekly for five weeks in locally advanced carcinoma cervix
Arm Title
Radiation HDR Brachytherapy 7 Gy
Arm Type
Active Comparator
Arm Description
High dose rate (HDR) brachytherapy of weekly 7 Gray in three fractions in three weeks after 50 Gray EBRT of 2 Gray per fraction of 25 fractions concurrently with weekly chemotherapy cisplatin40 mg /m2 in five weeks in locally advanced carcinoma cervix
Intervention Type
Radiation
Intervention Name(s)
HDR Brachytherapy of 9 Gy in 2 fractions
Intervention Description
Two fractions of HDR brachytherapy following standard dose CCRT in locally advanced carcinoma cervix
Intervention Type
Radiation
Intervention Name(s)
HDR Brachytherapy of 7 Gy in 3 fractions
Intervention Description
Three fractions of HDR Brachytherapy following standard dose CCRT in locally advanced carcinoma cervix
Primary Outcome Measure Information:
Title
Reduction of tumor size in cervix
Description
Comparison of pre treatment tumor size with post treatment tumor
Time Frame
Six month

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Locally advanced carcinoma cervix (stage 2b - 4a) Histopathology squamous cell carcinoma Exclusion Criteria: Previous history of malignancy Previously treated with radiotherapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohammad Abdul Bari, MBBS,MPhil
Organizational Affiliation
Associate Professor,dept.of Oncology,BSMMU
Official's Role
Study Director
Facility Information:
Facility Name
BSM Medical University
City
Dhaka
ZIP/Postal Code
1200
Country
Bangladesh

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
15850912
Citation
Patel FD, Rai B, Mallick I, Sharma SC. High-dose-rate brachytherapy in uterine cervical carcinoma. Int J Radiat Oncol Biol Phys. 2005 May 1;62(1):125-30. doi: 10.1016/j.ijrobp.2004.09.017.
Results Reference
result
Links:
URL
http://www.bsmmu.edu.bd
Description
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A Randomised Controlled Trial Between Two Different HDR Brachytherapy Schedule in Locally Advanced Carcinoma of Uterine Cervix

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