Cervical Cancer Brachytherapy With Interstitial Needles in 3 Fractions: Dosimetric and Clinical Outcomes

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Aim To determine the feasibility and safety of 3 fractions of high dose rate (HDR) brachytherapy with interstitial needles for cervical cancer in the outpatient setting Primary objective To determine the clinical outcome (2-yr local control rate, loco-regional control rate, progression free survival and overall survival) Secondary objective To determine the long-term toxicities of this regimen based on CTCAE v5

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 21
Healthy Volunteers: f
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• 21 years old and above

• Histologically proven squamous cell carcinoma, adenocarcinoma, adenosquamous or poorly differentiated cervical cancer

• Clinically or radiologically stage IB - IVA cervical cancer based on TNM 8th Edition

• ECOG performance status 0, 1, or 2

• To complete external beam radiotherapy and brachytherapy in NUH

• Written, voluntary informed consent

• Patients must be accessible for follow up and management in NUH

Locations
Other Locations
Singapore
National University Hospital
RECRUITING
Singapore
Contact Information
Primary
Fatin Aliyah, BSc
fatin_hussin@nuhs.edu.sg
+6581005851
Time Frame
Start Date: 2023-06-26
Estimated Completion Date: 2026-12
Participants
Target number of participants: 56
Treatments
Experimental: 3 fractions
Related Therapeutic Areas
Sponsors
Leads: National University Hospital, Singapore

This content was sourced from clinicaltrials.gov

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