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Spots Global Cancer Trial Database for Proton Beam Teletherapy for Post-Hysterectomy Cancers of the Uterus and Cervix

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Trial Identification

Brief Title: Proton Beam Teletherapy for Post-Hysterectomy Cancers of the Uterus and Cervix

Official Title: Pilot Study of Adjuvant Proton Beam Teletherapy for Post-Hysterectomy Cancers of the Uterus and Cervix With Metastases to Regional Lymph Nodes

Study ID: NCT01600040

Study Description

Brief Summary: Proton beam radiation therapy is known to spare surrounding normal tissues from radiation. Proton beam radiation delivers less radiation beyond the area of the target tissues. This may reduce side effects that patients would normally experience with standard (photon) radiation therapy which tends to unavoidably include more normal tissue along with tumor target tissue. In this research study, the investigators are looking to determine if proton beam radiation is effective in controlling your cancer growth. The investigators are also looking to see if proton beam radiation can reduce side effects when compared to standard radiation treatment (photon radiation).

Detailed Description: Subjects will receive proton beam radiation treatment as an outpatient at the Francis H. Burr Proton Center at Massachusetts General Hospital, 5 days per week (Mon-Fri) over 5-6 weeks depending on the type of cancer. Tests and procedures during study treatment (weekly): * Questions about health and current medications * Physical exam, includes height, weight and vital signs * Performance status * Blood test for complete blood counts and blood clotting (2 tsps). Repeated twice weekly for uterine cancer subjects and once weekly for cervix cancer subjects * Pelvic exam (at week 6 only) * Quality of life questionnaires After completion of proton beam radiation treatment, subjects will be followed for 5 years. Follow-up visits will occur every 3 months for 2 years; every 4 months to year 3 and every 6 months thereafter. At each visit subjects will receive: * A medical history * Physical exam * Performance status * Pelvic exam * CT scan of the chest, abdomen and pelvis every 6 months to year 3 * Quality of life questionnaires (6, 12, 24, 36, 48, and 60 months)

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Massachusetts General Hospital, Boston, Massachusetts, United States

Contact Details

Name: Andrea Russo, MD

Affiliation: Massachusetts General Hospital

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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