Magnetic Resonance Imaging-Based Radiation Therapy and Cisplatin in Patients With Stage I, Stage II, Stage III, or Stage IV Cervical Cancer
Stopped early · Not applicable
Conditions studied: Cervical Cancer
In brief
Rationale: Computer systems that allow doctors to create a 3 dimensional (3-D) picture of the tumor may help in planning radiation therapy and may result in more tumor cells being killed. Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue. Drugs, such as cisplatin, may make tumor cells more sensitive to radiation therapy.
Key facts
- Study ID
- NCT01016561
- Run by
- Abramson Cancer Center at Penn Medicine
- People needed
- 12
- Starts
- 2009-07-01
- Expected to finish
- 2016-12-01
- Last updated by the study team
- 2021-05-05
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Subjects must have histologically confirmed squamous cell, adenosquamous or adenocarcinoma of the cervix
- Subjects must have non-metastatic FIGO Stage Ia-IVa cervical cancer
- Claustrophobic subjects must agree to be sedated during MRI procedures
- ECOG performance status of 0-2
You may not qualify if…
- Subjects with an inability to tolerate MR imaging
- Subjects who have had prior surgery for treatment of disease other than exploratory laparotomy or biopsy
- Study subjects who have contraindication to MRI scanning such as but not limited to subjects with pacemakers, metal fragments in the eye or certain metallic implants
- Women of childbearing potential who have a positive result on screening serum pregnancy test
Where it is running
- Abramson Cancer Center of the Unviersity of Pennsylvania — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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