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Cervical Cancer Brachytherapy With Interstitial Needles in 3 Fractions

RECRUITINGN/ASponsored by National University Hospital, Singapore
Actively Recruiting
PhaseN/A
SponsorNational University Hospital, Singapore
Started2023-06-26
Est. completion2026-06
Eligibility
Age21 Years+
SexFEMALE
Healthy vol.Accepted
View on ClinicalTrials.gov →

NCT06284031

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

Age: 21 Years+Sex: FEMALEHealthy volunteers accepted
Inclusion Criteria:

1. 21 years old and above
2. Histologically proven squamous cell carcinoma, adenocarcinoma, adenosquamous or poorly differentiated cervical cancer
3. Clinically or radiologically stage IB - IVA cervical cancer based on TNM 8th Edition
4. ECOG performance status 0, 1, or 2
5. To complete external beam radiotherapy and brachytherapy in NUH
6. Written, voluntary informed consent
7. Patients must be accessible for follow up and management in NUH

Exclusion Criteria:

1. Post operative cervical cancer cases
2. Pregnant or breastfeeding women

Conditions2

CancerCervical Cancer

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