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Uterine Cervical Dysplasia clinical trials

View clinical trials related to Uterine Cervical Dysplasia.

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NCT ID: NCT01723956 Completed - Clinical trials for Cervical Intraepithelial Neoplasia

Validation of Implementation of Cervical Dysplasia Treatment Modalities in HIV-Seropositive Women

VICAR2
Start date: March 2010
Phase: N/A
Study type: Interventional

To compare the efficacy of cryotherapy and large loop excision of the transformation zone (LLETZ) procedures for the treatment of high-grade cervical intra-epithelial neoplasia (CIN2/3) among HIV-seropositive women by follow-up VIA, cytology and Human Papillomavirus. Hypothesis: LEEP will be more effective than cryotherapy in removing CIN 2/3 lesions in HIV positive women in South Africa

NCT ID: NCT01639820 Completed - Clinical trials for Uterine Cervical Dysplasia

Comparison of Pelvic Lymphadenectomy Versus Isolated Sentinel Lymph Node Biopsy Procedure for Early Stages of Cervical Cancers : a Multicenter Study With Evaluation of Medico-economic Impacts

SENTICOL2
Start date: January 2009
Phase: N/A
Study type: Interventional

Patients with early cervical cancer are usually treated with radical hysterectomy + pelvic lymph-node dissection. The study randomizes patients in 2 arms. The control arm is the classical surgical treatment including identification of the sentinel nodes, full pelvic lymph-node dissection and radical hysterectomy. The experimental arm is only sentinel node identification + radical hysterectomy.

NCT ID: NCT01628432 Completed - Cervical Dysplasia Clinical Trials

Effect of Salpingectomy During Conservative Hysterectomy

SALPINGOVA
Start date: July 2012
Phase: N/A
Study type: Interventional

The study compares the effect of bilateral salpingectomy associated with conservative hysterectomy on ovarian function to the standard hysterectomy with conservation of both ovaries and tubes in terms of hormone assays, ovarian ultrasound evaluation, complications, quality of life.

NCT ID: NCT01524003 Completed - Cervical Cancer Clinical Trials

Chinese Cancer Prevention Study(CHICAPS)

CHICAPS
Start date: November 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to develop and implement a community based preventive healthcare model using cervical cancer screening as the target medical intervention. The investigators will first conduct 2 pilot studies to refine their preventive healthcare model based on the principles of community based participatory research (1000 participants). The investigators will then apply the model to screen 9000 women for cervical cancer over a period of 7-9 days. This 10,000 patient trial will explore the ability of a community to conduct their own screening program to identify who needs medical intervention based on self-collection and centralized high-throughput low cost human papillomavirus (HPV) testing.

NCT ID: NCT01511328 Active, not recruiting - Clinical trials for High-grade Cervical Intraepithelial Neoplasia

Randomized Implementation of Primary HPV Testing in the Organized Screening for Cervical Cancer in Stockholm

Start date: January 1, 2012
Phase: N/A
Study type: Interventional

The purpose is to evaluate whether implementation of primary human papillomavirus (HPV) screening in the screening programme for cervical cancer improves the programme in terms of better cancer protection and better cost efficiency.

NCT ID: NCT01505920 Completed - Clinical trials for Uterine Cervical Dysplasia

Lidocaine Spray Compared With Submucosal Injection During LEEP: a Randomized Controlled Trial

Start date: September 2011
Phase: Phase 3
Study type: Interventional

Loop Electrosurgical Excision Procedure (LEEP) is a widely used minor surgical procedure for diagnosis and treatment of cervical intraepithelial neoplasia. During the procedure, several methods have been proposed to reducing pain including submucosal block, paracervical block, and oral analgesics. Submucosal (underneath the lining of the cervix) injection of lidocaine appeared to be the most common methods used. However, from the investigators experience, there is significant pain associated with the injection itself. Lidocaine spray is an effective measure for pain control during minor gastrointestinal and otolaryngological procedures. It is simple without pain related to application. An objective of this study is to examine effectiveness of lidocaine spray versus lidocaine submucosal injection by comparing pain scores at various stages of the LEEP procedure.

NCT ID: NCT01435590 Completed - Cervical Dysplasia Clinical Trials

Endocervical Evaluation With the Curette Versus Cytobrush for the Diagnosis of Dysplasia of the Uterine Cervix

Start date: September 2011
Phase: N/A
Study type: Interventional

OBJECTIVE: to compare endocervical brushing with endocervical curettage with respect to diagnostic and patient discomfort. METHOD: women referred to colposcopy because of abnormal Papanicolaou tests will be randomized to endocervical sampling with either a metal curette (endocervical curettage -ECC) or and endocervical brush. All samples will be submitted for histological study.

NCT ID: NCT01405768 Completed - Clinical trials for Uterine Cervical Dysplasia

Buffered Lidocaine for Loop Electrosurgical Excision Procedures (LEEPs)

Start date: July 2011
Phase: Phase 2
Study type: Interventional

Women undergoing a LEEP procedure who receive lidocaine buffered with sodium bicarbonate for their cervical block will experience less injection pain than women who receive plain lidocaine.

NCT ID: NCT01385436 Recruiting - Cervical Cancer Clinical Trials

Distribution of Human Papillomavirus (HPV) Genotypes in Patients With Cervical Cancer From Croatia

HPV-cancer
Start date: May 2010
Phase: N/A
Study type: Observational

Human papillomavirus (HPV) of high-risk genotype is a necessary risk factor in development of cervical cancer. There is a vaccine available to prevent cervical lesions associated with high-risk HPV genotypes 16 and 18. In Croatia HPV vaccination has not yet been introduced in obligatory vaccination schedule. The aim of this study is to describe the pre-vaccination distribution of HPV genotypes in women with high grade cervical squamous intraepithelial lesion (HSIL) and cervical cancer in Croatia. The investigators hypothesis is that HPV-16 is the most frequently found genotype but the distribution of other HPV genotypes is heterogeneous and includes genotypes currently not covered by vaccination.

NCT ID: NCT01371695 Enrolling by invitation - Cervical Cancer Clinical Trials

Serum IGF-II and Cancer: Can IGF II Levels be Used to Monitor and Screen Patients Specifically for Cervical Cancer

Start date: May 2011
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether Insulin-like Growth Factor II is elevated sufficiently to detect Cervical Intraepithelial Neoplasia II (CIN II), Cervical Intraepithelial Neoplasia III (CIN III), and cervical cancer.