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Hot Flashes clinical trials

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NCT ID: NCT00455689 Completed - Hot Flashes Clinical Trials

Understanding Experimentally Induced Hot Flushes

Start date: November 28, 2005
Phase: Phase 4
Study type: Interventional

The purpose of the study is to examine the impact of hot flushes on sleep, mood, and well-being. The investigators will cause hot flushes by giving study participants the hormone medication, leuprolide (Lupron), which is a manufactured (artificial) hormone that makes the body think that it has reached menopause temporarily. Most women begin to have hot flushes within 4 weeks after taking leuprolide and resume menses 3 months later. The investigators will administer questionnaires to evaluate changes in sleep and mood over the course of the study.

NCT ID: NCT00446199 Completed - Hot Flashes Clinical Trials

Low-dose Hormone Therapy for Relief of Vasomotor Symptoms

Start date: March 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the lowest effective dose of the study drug for the relief of moderate to severe vasomotor symptoms in postmenopausal women for 12 weeks.

NCT ID: NCT00427622 Completed - Hot Flashes Clinical Trials

Skin Conduction Device for Measuring Hot Flashes in Postmenopausal Women With Hot Flashes

Start date: May 2006
Phase: N/A
Study type: Interventional

RATIONALE: Measuring how often hot flashes occur in postmenopausal women may be done by using a skin conduction device or by using a diary. PURPOSE: This clinical trial is comparing a skin conduction device with a hot flash diary as a way of measuring hot flashes in postmenopausal women with hot flashes.

NCT ID: NCT00427531 Completed - Hot Flashes Clinical Trials

Skin Conduction Device and Patient Diary for Measuring Hot Flashes in Postmenopausal Women With Hot Flashes

Start date: June 2006
Phase: N/A
Study type: Interventional

RATIONALE: Measuring how often hot flashes occur in postmenopausal women may be done by using a skin conduction device or by using a diary. PURPOSE: This clinical trial is studying a skin conduction device and a patient diary for measuring hot flashes in postmenopausal women with hot flashes.

NCT ID: NCT00421902 Completed - Prostate Cancer Clinical Trials

Acupuncture Treatment for Hot Flashes Study

Start date: January 2006
Phase: N/A
Study type: Interventional

Patients with prostate cancer who are / were treated with hormonal treatment and developed hot flashes as a side effect are offered Acupuncture as an investigational intervention. The treatment is performed twice a week for four weeks, then once a week for the following six weeks

NCT ID: NCT00391417 Completed - Hot Flashes Clinical Trials

Efficacy and Safety of a Topical Estradiol Gel for Treatment of Postmenopausal Symptoms

Start date: September 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the efficacy and safety of a topical estradiol gel for the treatment of hot flushes in postmenopausal women.

NCT ID: NCT00378846 Completed - Clinical trials for Fever, Sweats, and Hot Flashes

Three Different Types of Thermometers in Measuring Temperature in Young Patients With Fever and Without Fever

Start date: March 2006
Phase: N/A
Study type: Interventional

RATIONALE: Comparing results of three different thermometers used to measure body temperature may help doctors find the most accurate thermometer to detect fever and plan the best treatment. PURPOSE: This clinical trial is studying three different types of thermometers to measure temperature in young patients with fever and without fever.

NCT ID: NCT00363909 Completed - Breast Cancer Clinical Trials

Citalopram in Treating Postmenopausal Women With Hot Flashes

Start date: November 2006
Phase: Phase 3
Study type: Interventional

RATIONALE: Citalopram may help relieve hot flashes in women who had or have not had breast cancer. It is not yet known which dose of citalopram is more effective in treating hot flashes in postmenopausal women. PURPOSE: This randomized phase III trial is studying three different doses of citalopram to compare how well they work in treating postmenopausal women with hot flashes.

NCT ID: NCT00354432 Terminated - Prostate Cancer Clinical Trials

Soy Protein/Effexor Hormone Therapy for Prostate Cancer

Start date: February 1, 2007
Phase: Phase 3
Study type: Interventional

RATIONALE: Soy protein/isoflavones and venlafaxine may help relieve hot flashes in patients receiving hormone therapy for prostate cancer. It is not yet known whether soy protein/isoflavones are more effective than venlafaxine when given together or with a placebo in treating hot flashes. PURPOSE: This randomized phase III trial is studying soy protein/isoflavones and venlafaxine to compare how well they work when given together or with a placebo in treating hot flashes in patients receiving hormone therapy for prostate cancer.

NCT ID: NCT00335478 Completed - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Daptomycin in Treating Neutropenia and Fever in Patients With Cancer

Start date: December 2006
Phase: Phase 2
Study type: Interventional

RATIONALE: Antibiotics, such as daptomycin, may control neutropenia, fever, and infection in patients with cancer. PURPOSE: This phase II trial is studying how well daptomycin works in treating neutropenia and fever in patients with cancer.