| CTRI Number |
CTRI/2025/12/098658 [Registered on: 08/12/2025] Trial Registered Prospectively |
| Last Modified On: |
08/12/2025 |
| Post Graduate Thesis |
No |
| Type of Trial |
Observational |
|
Type of Study
|
Cohort Study |
| Study Design |
Single Arm Study |
|
Public Title of Study
|
Testing Computer Programs that Automatically Identify Body Organs in Cancer Patients Scans to Improve Radiation Therapy Planning |
|
Scientific Title of Study
|
Deep Learning For Radiotherapy Autosegmentation Workflow : Prospective Multicenter Evaluation Study Protocol |
| Trial Acronym |
DRAW ME |
|
Secondary IDs if Any
|
| Secondary ID |
Identifier |
| NIL |
NIL |
|
|
Details of Principal Investigator or overall Trial Coordinator (multi-center study)
|
| Name |
Santam Chakraborty |
| Designation |
Senior Consultant |
| Affiliation |
Tata Medical Center |
| Address |
Department of Radiation Oncology, Tata Medical Center, Kolkata, West Bengal
North Twentyfour Parganas WEST BENGAL 700160 India |
| Phone |
03366057402 |
| Fax |
|
| Email |
drsantam@gmail.com |
|
Details of Contact Person Scientific Query
|
| Name |
Santam Chakraborty |
| Designation |
Senior Consultant |
| Affiliation |
Tata Medical Center |
| Address |
Department of Radiation Oncology, Tata Medical Center, Kolkata, West Bengal
WEST BENGAL 700160 India |
| Phone |
03366057402 |
| Fax |
|
| Email |
drsantam@gmail.com |
|
Details of Contact Person Public Query
|
| Name |
Santam Chakraborty |
| Designation |
Senior Consultant |
| Affiliation |
Tata Medical Center |
| Address |
Department of Radiation Oncology, Tata Medical Center, Kolkata, West Bengal
WEST BENGAL 700160 India |
| Phone |
03366057402 |
| Fax |
|
| Email |
drsantam@gmail.com |
|
|
Source of Monetary or Material Support
|
|
|
Primary Sponsor
|
| Name |
Tata Medical Center |
| Address |
Department of Radiation Oncology,
Tata Medical Center, Kolkata, West Bengal 700160 |
| Type of Sponsor |
Private hospital/clinic |
|
|
Details of Secondary Sponsor
|
|
|
Countries of Recruitment
|
India |
|
Sites of Study
|
| No of Sites = 1 |
| Name of Principal
Investigator |
Name of Site |
Site Address |
Phone/Fax/Email |
| Santam Chakraborty |
Tata Medical Center |
Department of Radiation Oncology,
Tata Medical Center, Kolkata, West Bengal North Twentyfour Parganas WEST BENGAL |
03366057402
santam.chakraborty@tmckolkata.com |
|
|
Details of Ethics Committee
|
| No of Ethics Committees= 1 |
| Name of Committee |
Approval Status |
| Tata Medical Center IRB |
Approved |
|
|
Regulatory Clearance Status from DCGI
|
|
|
Health Condition / Problems Studied
|
| Health Type |
Condition |
| Patients |
(1) ICD-10 Condition: D499||Neoplasm of unspecified behavior of unspecified site, |
|
|
Intervention / Comparator Agent
|
| Type |
Name |
Details |
| Intervention |
NIL |
NIL |
|
|
Inclusion Criteria
|
| Age From |
18.00 Year(s) |
| Age To |
99.00 Year(s) |
| Gender |
Both |
| Details |
The target population is patients with cancer being treated with radiotherapy for whom automatic segmentation models are available in the DRAW system. Currently this includes:
1. CNS malignancies
2. Breast cancers
3. Head Neck cancers
4. Lung cancers
5. Esophageal cancers
6. Prostate cancers
7. Gynecological cancers
8. Rectal cancers |
|
| ExclusionCriteria |
| Details |
Model not available for the cancer site for automatic segmentation |
|
|
Method of Generating Random Sequence
|
Not Applicable |
|
Method of Concealment
|
Not Applicable |
|
Blinding/Masking
|
Not Applicable |
|
Primary Outcome
|
| Outcome |
TimePoints |
| Qualitative Validation: Number of cases where no or minor modifications were required. |
24 months |
|
|
Secondary Outcome
|
| Outcome |
TimePoints |
| Quantitative Validation: Average volumetric dice similarity between the autosegmented contours and the manually segmented structure sets. This will be compared against the reference VDS value. |
24 months |
| Time taken for modification: The estimated time required for making the modifications required for the cases after automatic segmentation will be reported. |
24 months |
|
|
Target Sample Size
|
Total Sample Size="1000" Sample Size from India="1000"
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" |
|
Phase of Trial
|
N/A |
|
Date of First Enrollment (India)
|
01/01/2026 |
| Date of Study Completion (India) |
Applicable only for Completed/Terminated trials |
| Date of First Enrollment (Global) |
Date Missing |
| Date of Study Completion (Global) |
Applicable only for Completed/Terminated trials |
|
Estimated Duration of Trial
|
Years="2" Months="0" Days="0" |
|
Recruitment Status of Trial (Global)
|
Not Applicable |
| Recruitment Status of Trial (India) |
Not Yet Recruiting |
|
Publication Details
|
N/A |
|
Individual Participant Data (IPD) Sharing Statement
|
Will individual participant data (IPD) be shared publicly (including data dictionaries)?
Response - NO
|
|
Brief Summary
|
Automatic segmentation is gaining increasing acceptance in Radiation Oncology to reduce burden and improve consistency. However commercial systems are expensive and inflexible. Open source systems are flexible but require a significant technological know-how for implementation. The team from Tata Medical Center Kolkata and IIT Kharagpur have developed a deep-learning based autosegmentation system which can be deployed with minimal capital expenditure and uses a distributed client-server architecture to allow fast parallel processing of cases. At the time of this version, the DRAW system uses nnU-Net for the deep-learning-based modelling.
Aims To evaluate the real world use of the DRAW system in a real world setting
Objectives To determine if the DRAW system can be successfully installed and configured at multiple hospitals (Implementation objective) To determine if the system performance is considered acceptable for the users at the hospitals where the DRAW system was installed (Validation objective)
Endpoints To determine the percentage of centers where the DRAW system was successfully installed and configured. The DRAW client system should be installed and work with the DICOM data storage system available at the participating center to be considered as a successful install. Qualitative: At least 50% of the cases were segmented with no or minor modifications/errors as determined qualitatively by the end users. Quantitative: At least 70% of the segmented structures have an average volumetric dice similarity score (VDS) not less than 0.10 points below the reference VDS. The reference value will be defined based on the VDS reported in the literature (or if not available in the literature then the model validation statistics obtained from the DRAW segmentation pipeline).
Design Multicenter, single-arm, prospective cohort study Methods The DRAW system will be installed in the participating hospitals and configured to integrate it with the planning workflow. Autosegmentation will be performed by the DRAW system and this will be reviewed by the oncologists at the participating center. Qualitative evaluation of the contours will be performed by the oncologists. De-identified DICOM data will be used to determine the spatial similarity between autosegmented and manually segmented structures for quantitative evaluation.
Statistical Analysis Descriptive summary statistics will be presented for each endpoint along with appropriate visualization. For proportions we will also report the corresponding binomial 95% confidence intervals. For quantitative data, the median, mean and 95% confidence intervals of the mean shall be reported.
Sample size The minimum sample size for the study is 1000 patients based on the quantitative validation objective.
Study Duration 2 years
|