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Cervix Neoplasms clinical trials

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NCT ID: NCT04295109 Recruiting - Endometrial Cancer Clinical Trials

Comparison of the Effects of Fentanyl, Oxycodone, Butorphanol on Gastrointestinal Function

Start date: March 2, 2020
Phase: N/A
Study type: Interventional

Postoperative ileus (POI) is a transient loss of coordinated peristalsis precipitated by surgery and exacerbated by opioid pain medication.So,how to provide patients with ideal analgesia without affecting the recovery of postoperative gastrointestinal function?This was a prospective randomized controlled study. A total of 105 patients who were scheduled for laparoscopic hysterectomy were randomly selected from The First Affiliated Hospital with Nanjing Medical University by random number table. These patients were randomly divided into three groups: fentanyl(F) group, oxycodone(O) group and butorphanol(B) group.

NCT ID: NCT02184975 Completed - Clinical trials for Cervical Intraepithelial Neoplasia

Cold Knife Conization With and Without Lateral Hemostatic Sutures

Start date: March 2009
Phase: Phase 2
Study type: Interventional

The treatment of high grade Cervical Intraepithelial Neoplasia (CIN) 2, 3 is defined according to the colposcopic evaluation of the patient. In case colposcopy findings are satisfactory (visible squamocolumnar junction), both ablative and excisional methods are adequate. In the middle of the 20th century, lateral hemostatic sutures were added to the cold knife conization surgical technique to reduce blood loss. Some authors recommend that these branches should be ligated, but it remains unclear whether these sutures are actually effective in reducing bleeding.This study compared blood loss during cold knife conization of the cervix with and without lateral hemostatic sutures.

NCT ID: NCT00288821 Completed - Ovarian Neoplasms Clinical Trials

Diagnostic Imaging of Lymph Nodes in Gynaecologic Oncology

Start date: February 2006
Phase: N/A
Study type: Observational

The purpose of the study is to determine the diagnostic accuracy of a new magnetic resonance imaging (MRI) technique, the diffusion weighted imaging with body background signal suppression (DWIBS) in the detection of lymph node pathology in patients with gynaecologic malignancies.

NCT ID: NCT00188695 Completed - Prostatic Neoplasms Clinical Trials

Combidex USPIO - Ultra-small Superparamagnetic Iron Oxide

Start date: April 2004
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to test whether or not a new contrast agent called Combidex, a contrast agent formulated from ultra-small superparamagnetic iron oxide (USPIO) improves the ability of Magnetic Resonance Imaging (MRI) to see lymph nodes in the pelvis. It might also help doctors tell whether or not cancer has spread to these lymph nodes. It might allow radiotherapy to be delivered more accurately.

NCT ID: NCT00188578 Completed - Uterine Neoplasms Clinical Trials

Intensity Modulated Radiation Therapy - Gyne Cancer (GY03.2)

Start date: June 2003
Phase: Phase 1/Phase 2
Study type: Interventional

Standard treatment for gynecological cancer is radiation therapy in two phases; whole pelvic radiation and then an internal radiation boost, also called a brachytherapy boost, to treat any remaining tumour. The purpose of this study is to test an alternative radiation boost treatment called conformal intensity modulated radiation therapy or IMRT. Currently, we do not have complete information on the overall effectiveness of IMRT compared to brachytherapy or conformal radiotherapy. We know that IMRT allows the radiation beams to be more accurately focused on the tumor, thereby sparing more normal tissue from radiation damage and lowering risks of side effects. We are investigating the extent to which IMRT can be used to protect normal tissues in patients with cervix, uterine or vaginal cancer from the radiation beams and how much the side effects of radiation are reduced.

NCT ID: NCT00188539 Active, not recruiting - Cervix Neoplasms Clinical Trials

Cervix:Hypoxia, Interstitial Fluid Pressure and GSH Levels

Start date: December 1995
Phase: Phase 2
Study type: Interventional

The aim of this study is to measure the oxygen content and interstitial fluid pressure in cervix cancer patients. Tumour oxygen content and internal pressure of tumours may be an important factor that influences the effectiveness of radiotherapy and other treatments.

NCT ID: NCT00178802 Active, not recruiting - Breast Neoplasms Clinical Trials

Chemotherapy With Whole Body Hyperthermia to Treat Resistant Breast, Endometrial, Cervical and Ovarian Cancers

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

Thermal therapy (hyperthermia of heat) can increase the effect of chemotherapy treatments. By itself, thermal therapy can also kill cancer cells. By using thermal therapy to treat the whole body, the investigators can treat cancer cells wherever they are throughout the entire body. In this study, the investigators are testing the combination of thermal therapy combined with chemotherapy to see: 1. if it improves the effect of the chemotherapy drugs, 2. if it helps the body fight the cancer cells, and 3. if this treatment is safe for the patient. This study does not offer heat treatment alone. Any patient with advanced or metastatic breast, or endometrial cancer resistant to standard treatment may be treated with the phase II protocol therapy; however, the patient will need to undergo some medical tests to make sure this treatment would be safe for them.

NCT ID: NCT00152828 Completed - Cervix Neoplasms Clinical Trials

Celebrex - Cervix: Celecoxib in the Treatment of Patients With Locally Advanced Carcinoma of the Cervix

Start date: February 2001
Phase: Phase 1/Phase 2
Study type: Interventional

This is a phase I/II study to evaluate the safety and toxicity of celecoxib in combination with standard concurrent cisplatin and radiotherapy in women with locally advanced cervix cancer. In addition, we aim to determine the effect of celecoxib (Celebrex) on tumour oxygenation, interstitial fluid pressure, COX-2 levels, prostaglandin E2 levels, angiogenesis and apoptosis.

NCT ID: NCT00127465 Completed - Breast Neoplasms Clinical Trials

Investigating the Impact of Tailored Reports on Anxiety Amongst Cancer Patients and Their Confidants

Start date: November 2001
Phase: Phase 1/Phase 2
Study type: Interventional

Objective: To explore the hypothesis that different methods of selecting and printing information for cancer patients could improve emotional support by affecting interaction with others, and so lead to improved psychological wellbeing. Design: Randomised trial with 8 groups (three factors, 2X2X2). Data collected at recruitment and three month follow-up. Participants: 400 patients starting radiotherapy and their 'confidant' (the person in who they confide). Interventions: Printed booklets. 1. Half had 'general' CancerBACUP information for that cancer; half had 'personal' information from the medical record plus selected general information; 2. Half chose information by 'interacting' with the computer; half had a larger volume of material in booklets that were produced 'automatically'. 3. Half had additional 'anxiety management advice'. Outcomes: Patients' views; use of booklet with others; change in reported social support; change in anxiety and depression.

NCT ID: NCT00119509 Active, not recruiting - Cervix Neoplasms Clinical Trials

The IMAP Study Improving Management of Mildly Abnormal Pap Smears

Start date: January 2004
Phase: Phase 3
Study type: Interventional

The study compares the psychosocial outcomes of different management strategies for women with minor atypia (including ‘HPV effect’) detected on Pap smears: conventional management (a repeat Pap smear at 6 months) versus Human papillomavirus (HPV) DNA testing, a new method proposed for the management of minor atypia and the informed choice of either management supported by a decision aid. The study examines women’s informed preferences for each of these options and compares the psychosocial outcomes in women who are or are not given the choice of management. HPV DNA testing offers considerable changes to the management of women with minor atypia and there is evidence from the USA which suggests that the use of HPV DNA testing as a triage strategy is effective for women within this group (Solomon et al 2001). The introduction of HPV DNA testing may bring both benefits and harms to women. These harms and benefits are not well understood. Examination of the psychosocial outcomes of HPV DNA testing compared to conventional management and women’s preferences for each is needed to guide decisions concerning HPV DNA testing in cervical screening in Australia and also internationally.