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Chemotherapy-induced Symptoms in Sarcoma Patients and the Impact of Tumor Burden

Chemotherapy-induced Symptoms in Sarcoma Patients and the Impact of Tumor Burden

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01136824
Enrollment
11
Registered
2010-06-03
Start date
2010-06-30
Completion date
2014-05-31
Last updated
2016-07-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Soft Tissue Sarcoma

Keywords

Sarcoma, questionnaire, doxorubicin plus ifosfamide (AI)

Brief summary

Assessments (survey data) in this study are designed to sample the symptom burden of patients undergoing adjuvant and neoadjuvant chemotherapy in the hospital. There will be no change in the treatment plan for these patients.

Interventions

OTHERQuestionnaires

Subjects will be given a series of questionnaires to assess the effect of AI chemotherapy, and the possible role of tumor load, on the amount of symptoms. The extent of nausea, vomiting, fatigue, anxiety, sleep disturbance, and cognitive changes will be measured. In adjuvant chemotherapy patients, we will also assess the relationship between tumor size and amount of chemotherapy-induced symptoms. These questionnaires will involve the following assessments: Demographic & health Trait anxiety Quality of life Nausea Expectations Anxiety & total mood disturbance Nausea & vomiting Multiple symptoms

Sponsors

University of Pittsburgh
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients who are receiving doxorubicin plus ifosfamide (AI)

Exclusion criteria

* There is no

Design outcomes

Primary

MeasureTime frame
To determine the extent of symptom burden and quality of life in sarcoma patients receiving AI chemotherapy.2 years

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026