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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00165269
Other study ID # 92-035
Secondary ID
Status Completed
Phase Phase 2
First received September 9, 2005
Last updated October 30, 2009
Start date May 1992
Est. completion date February 2008

Study information

Verified date October 2009
Source Dana-Farber Cancer Institute
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study it to evaluate the effectiveness of radiation therapy limited to above the diaphragm in patients with pathological stage IA-IIA Hodgkin's disease.


Description:

- Eligble patients will receive a course of radiation therapy directed to above the diaphragm only.

- Patients would have bloodwork and chest x-rays performed 4 times per year for the first two years, 3 times per year for the third year, and 2 times per year for the fourth and fifth years. After five years, yearly check-ups are performed.

- In addition to the above follow-up, patients will receive, once or twice a year for the first 5 years, an abdominal-pelvic CT scan and/or gallium scan.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date February 2008
Est. primary completion date June 2000
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Pathologically Stage IA-IIA Hodgkin's disease

- A negative staging laparotomy including splenectomy, biopsies of liver, paraortic nodal biopsies and palpitation of upper pelvic nodes

- 18 years of age or older

Exclusion Criteria:

- Patients with large mediastinal adenopathy

- Patients with LD histology

- Patients with "B" symptoms

- Positive laparotomy

- Subcarinal, hilar, or cardiac lymph node involvement

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Mantle irradiation
Limited to above the diaphragm

Locations

Country Name City State
United States Dana-Farber Cancer Center Boston Massachusetts
United States Massachusetts General Hospital Boston Massachusetts

Sponsors (3)

Lead Sponsor Collaborator
Dana-Farber Cancer Institute Brigham and Women's Hospital, Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary To evaluate the risks and benefits of mantle field irradiation alone in treating Hodgkin disease patients. 5 years Yes
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