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Quality of Life clinical trials

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NCT ID: NCT00006799 Completed - Quality of Life Clinical Trials

Megestrol to Limit Weight Loss and Improve Quality of Life in Treating Patients With Head and Neck Cancer

Start date: October 1, 2000
Phase: Phase 3
Study type: Interventional

RATIONALE: Megestrol helps improve appetite. It is not yet known if megestrol is effective in limiting weight loss caused by cancer. PURPOSE: Randomized phase III trial to determine the effectiveness of megestrol in limiting weight loss and improving quality of life in patients who have head and neck cancer and are undergoing radiation therapy.

NCT ID: NCT00004911 Completed - Colorectal Cancer Clinical Trials

Endoscopic Placement of Metal Stent in Patients With Cancer-Related Bowel Obstruction

Start date: January 2000
Phase: Phase 1/Phase 2
Study type: Interventional

RATIONALE: The use of endoscopy to place a metal stent in the large intestine is less invasive than surgery for treating cancer-related bowel obstruction and may have fewer side effects and improve recovery. PURPOSE: Phase I/II trial to study the effectiveness of endoscopic placement of a metal stent in treating patients who have cancer-related bowel obstruction.

NCT ID: NCT00004910 Completed - Colorectal Cancer Clinical Trials

Endoscopic Placement of Metal Stents in Treating Patients With Cancer- Related Duodenal Obstruction

Start date: January 2000
Phase: Phase 1/Phase 2
Study type: Interventional

RATIONALE: The use of endoscopy to place metal stents in the duodenum is less invasive than surgery for treating cancer-related duodenal obstruction and may have fewer side effects and improve recovery. PURPOSE: Phase I/II trial to study the effectiveness of endoscopic placement of metal stents in treating patients who have cancer-related obstruction of the duodenum.

NCT ID: NCT00004909 Completed - Quality of Life Clinical Trials

Effect of Chemotherapy Given Either by Mouth or by Infusion on the Quality of Life of Patients With Recurrent Ovarian Epithelial Cancer

Start date: November 1999
Phase: N/A
Study type: Observational

RATIONALE: Quality-of-life assessment in patients undergoing cancer treatment may help determine the intermediate- and long-term effects of the treatment on these patients. PURPOSE: This clinical trial studies the effects of chemotherapy given by mouth versus chemotherapy given by infusion on quality of life in patients with recurrent ovarian epithelial cancer.

NCT ID: NCT00004166 Completed - Quality of Life Clinical Trials

Amifostine in Treating Patients With Ovarian Epithelial Cancer Who Are Receiving Chemotherapy

Start date: October 1999
Phase: Phase 3
Study type: Interventional

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Chemoprotective drugs such as amifostine may protect normal cells from the side effects of chemotherapy. PURPOSE: Randomized phase III trial to study the effectiveness of amifostine in treating patients who have ovarian epithelial cancer and who are receiving chemotherapy.

NCT ID: NCT00003686 Terminated - Quality of Life Clinical Trials

Pilocarpine in Treating Patients With Dry Mouth Caused by Opioids

Start date: May 22, 1998
Phase: Phase 3
Study type: Interventional

RATIONALE: Pilocarpine may help to relieve dry mouth in patients receiving opioids for cancer therapy. It is not yet known whether pilocarpine is more effective than no further treatment for this condition. PURPOSE: Randomized phase III trial to determine the effectiveness of pilocarpine in treating patients who have dry mouth caused by opioids.

NCT ID: NCT00003685 Completed - Pain Clinical Trials

Radiation Therapy to Relieve Symptoms in Patients With Non-small Cell Lung Cancer

Start date: August 1, 1997
Phase: Phase 3
Study type: Interventional

RATIONALE: Radiation therapy may relieve symptoms in patients with non-small cell lung cancer. It is not yet known which regimen of radiation therapy is most effective in relieving symptoms in patients with non-small cell lung cancer. PURPOSE: Randomized phase III trial to compare the effectiveness of different regimens of radiation therapy to relieve symptoms in patients who have non-small cell lung cancer.

NCT ID: NCT00003684 Completed - Quality of Life Clinical Trials

Theophylline in Treating Cancer Patients With Shortness of Breath

Start date: March 24, 1998
Phase: Phase 3
Study type: Interventional

RATIONALE: Theophylline may help to relieve shortness of breath in patients who have cancer. It is not yet known whether theophylline is more effective than no further treatment for shortness of breath. PURPOSE: Randomized phase III trial to determine the effectiveness of theophylline in treating shortness of breath in patients who have cancer.

NCT ID: NCT00003232 Completed - Prostate Cancer Clinical Trials

Combination Chemotherapy in Treating Pain in Hormone Refractory Metastatic Prostate Cancer

Start date: November 24, 1997
Phase: Phase 3
Study type: Interventional

RATIONALE: Some drugs used in chemotherapy can reduce the pain experienced by some people with cancer. Combining more than one drug may be more effective at reducing cancer pain. It is not known whether receiving combination chemotherapy with clodronate is more effective than receiving combination chemotherapy without clodronate for hormone refractory metastatic prostate cancer. PURPOSE: Randomized double-blinded phase III trial to compare the effectiveness of combination chemotherapy using mitoxantrone plus prednisone with or without clodronate in treating pain in patients with hormone refractory metastatic prostate cancer.

NCT ID: NCT00000423 Completed - Quality of Life Clinical Trials

Support, Health, and Fibromyalgia

Start date: September 1996
Phase: Phase 2
Study type: Interventional

This study tests the effects of social support and education on the health and well-being of people with fibromyalgia (FMS). We recruited 600 adults with a confirmed diagnosis of FMS from a large health maintenance organization. We randomly assigned the study participants to one of three groups. People in the social support group met with others who suffer from FMS for 2 hours every week for 10 weeks, and then monthly for an additional 10 months. The social support and education group also had 10 2-hour weekly meetings followed by 10 monthly meetings with others who suffer from FMS. Members of this group learned about the disease and ways they can manage it themselves. The third group participated only in the five assessment periods. The study lasted 4 years.