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Gynecologic Cancer clinical trials

View clinical trials related to Gynecologic Cancer.

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NCT ID: NCT02351089 Terminated - Gynecologic Cancer Clinical Trials

Probiotics in Radiation-treated Gynecologic Cancer

ProRad
Start date: February 2015
Phase: N/A
Study type: Interventional

The aim of the current Project is to study the efficacy of a probiotic Product in reducing the symptoms of gastrointestinal toxicity linked to the irradiation of gynecologic cancer.

NCT ID: NCT02108457 Completed - Gynecologic Cancer Clinical Trials

[18F] Flourothymidine (FLT) PET/CT Imaging for Gynecologic Cancers

Start date: February 2014
Phase:
Study type: Observational

The purpose of this study is to determine the effect of specific bone marrow maps developed with18F-FLT PET/CT imaging on the ability to spare proliferating bone marrow using proton beam radiotherapy compared to IMRT. Participants will be 18 years of age or old with a history of gynecologic cancer. Subjects will undergo 3 FLT-PET scans (one before treatment, one during the course of RT, and one 2-5 weeks after initiation of RT). Scans will take place in the Department of Radiation Oncology.

NCT ID: NCT02103933 Not yet recruiting - Gynecologic Cancer Clinical Trials

Pilot Study to Evaluate the Knowledge and Understanding on Surgery for Patients With Hysterectomy

Start date: April 2014
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to assess the level of knowledge of surgery for women who underwent hysterectomy

NCT ID: NCT02083614 Unknown status - Gynecologic Cancer Clinical Trials

The Effect of Clamping the Indwelling Urethral Catheter Before Removal From Patients After Type III Radical Hysterectomy

Start date: November 2013
Phase: N/A
Study type: Interventional

The effect of clamping the indwelling urethral catheter before removal is an unsettled issue in clinical practice. No studies have done before in the patients with gynecologic cancers who received radical hysterectomy. We hypothesized that clamping the catheter would decrease the rate of recatheterization. In addition, the feeling of urination during clamping is correlated with lower rate of recatheterization after removal.

NCT ID: NCT02069171 Completed - Gynecologic Cancer Clinical Trials

Cross-sectional and Questionnaire Study for Leg Lymphedema

Start date: June 2012
Phase: N/A
Study type: Observational

The purpose of this study is to identify the incidence,feature,clinical significance for leg lymphedema after gynecologic cancer treatment.

NCT ID: NCT02067637 Withdrawn - Breast Cancer Clinical Trials

Delayed Effects of Treatment in Cancer Survivors (DETECS)

DETECS
Start date: March 2014
Phase: N/A
Study type: Observational

Hypotheses and Specific Aims: There is limited data on the long-term consequences of cancer therapy on young, reproductively aged cancer survivors. The investigators objective is to characterize some of these effects in the cancer population.

NCT ID: NCT01974193 Recruiting - Gynecologic Cancer Clinical Trials

Prevention of Pelvic Lymphocele by Floseal During Pelvic Lymphadenectomy for Gynecologic Cancer

Start date: December 2013
Phase: Phase 3
Study type: Interventional

Pelvic lymph node dissection (PLND) is an important step in the surgical staging and treatment of gynecologic malignancies. Sometimes, complicated lymphoceles after PLND often delay adjuvant treatment including chemotherapy and radiation therapy, which potentially affects the success of cancer treatment. A number of surgical techniques have developed, but failed to reduce the incidence of pelvic lymphoceles after PLND. The investigators hypothesized that floseal can prevent lymphoceles in patients with gynecologic cancer who has undergone PLND. The investigators designed prospective randomized controlled study as a pilot study. The investigators will randomly apply floseal to one side of pelvis after bilateral PLND, and observe the occurence of pelvic lymphoceles after 6 months later.

NCT ID: NCT01951807 Completed - Gynecologic Cancer Clinical Trials

Psychological Interventions for Gynecologic Cancer

Start date: June 2010
Phase: N/A
Study type: Interventional

Subjects that have received medical treatment for ovarian cancer can be both physically and emotionally demanding for patients. The purpose of this study is to determine whether two common pyschological interventions (Communication Skills Intervention and Supportive Counseling) may improve the well-being of ovarian cancer patients compared to usual care.

NCT ID: NCT01849224 Recruiting - Gynecologic Cancer Clinical Trials

Randomized Trial of Exercise on Lower Extremity Edema After Lymphadenectomy in Gynecologic Cancer

Start date: May 2013
Phase: Phase 3
Study type: Interventional

The primary outcome is the change in lower extremity edema-related symptoms. Secondary outcomes include the compliance rate of management guidelines for lower extremity edema, the performance rate for pelvic and lower extremity exercise.

NCT ID: NCT01833637 Completed - Breast Cancer Clinical Trials

Electronic Patient Reported Symptom Assessment

Start date: October 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to assess whether using computerized screening questions can improve how well we manage symptoms related to cancer and cancer treatments. Advance care planning is a process in which teams of experts assist in with treatment plans, managing pain and other symptoms, emotional issues, and end of life issues. With advances in technology, it is now possible to get the patient's feedback directly and more often. It is thought that repeated questionnaires completed by the patient will provide a better and more accurate measure of the patient's needs and experiences but this has not been tested. This study is designed to learn if using a computerized assessment repeatedly is better than standard planning techniques.