Comparison of Clinical Response and Toxicity of Hypo-fractionated Chemoradiation With Standard Treatment in Patients With Uterine Cervix Cancer

Status: Recruiting
Location: See location...
Intervention Type: Radiation
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Uterine cervix cancer can be treated definitively with concurrent chemoradiation (external beam radiotherapy and chemotherapy) followed by high dose rate brachytherapy. Treatment duration can be shortened by increasing the dose per fraction of treatment which can reduce costs and patient exposure. The aim of our study is to determine the non-inferiority of hypofractionated radiotherapy compared with conventional treatment.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: t
View:

• Pathology of squamous cell carcinoma (SCC), adenocarcinoma, adenosquamous carcinoma of uterine cervix- International Federation of Gynecology and Obstetrics (FIGO) stage IB, IIA, IIB, IIIA, IIIB (due to hydronephrosis without creatinine clearance compromise), IIIC1 (if less than 3 lymph nodes with size less than 3cm, and without involvement of common iliac chain)- Patient eligible for definitive chemoradiotherapy followed by brachytherapy

Locations
Other Locations
Islamic Republic of Iran
Imam Khomeini Hospital Complex
RECRUITING
Tehran
Contact Information
Primary
Kasra Kolahdouzan, M.D.
k-kolahdouzan@razi.tums.ac.ir
+989144083785
Backup
Ebrahim Esmati, M.D.
eb_esmati@yahoo.com
+989126880306
Time Frame
Start Date: 2021-04-01
Estimated Completion Date: 2028-03
Participants
Target number of participants: 60
Treatments
Experimental: Hypofractionated
EBRT 40Gy/15fr
Active_comparator: Control Group
EBRT 45Gy/ 25fr
Related Therapeutic Areas
Sponsors
Leads: Tehran University of Medical Sciences

This content was sourced from clinicaltrials.gov