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Uterine Cervical Neoplasms clinical trials

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NCT ID: NCT02705612 Recruiting - Cervical Cancer Clinical Trials

Phase II Clinical Trial of Concurrent Chemoradiotherapy Combined Nimotuzumab for Stage IIB-IVA Cervical Cancer

Start date: September 2015
Phase: Phase 2
Study type: Interventional

The purpose of this phase II trial is to determine the feasibility and efficacy of nimotuzumab injection combined with concurrent chemoradiotherapy for initially inoperable locally advanced cervical cancer.

NCT ID: NCT02703961 Recruiting - Cervical Cancer Clinical Trials

Randomized Control Trial on Efficacy and Safety of Concurrent and Adjuvant Chemotherapy for the Cervical Cancer

Start date: February 2016
Phase: Phase 3
Study type: Interventional

The standard treatment of local advanced cervical cancer is concurrent chemoradiotherapy. The 3 year disease free survival was about 50-70%. The distant metastasis is the main cause of failure in local advanced cervical cancer treated with 3-dimensional conformal radiotherapy (3D-CRT) or intensity modulated radiotherapy (IMRT). The purpose of this study is to investigate the efficacy and tolerance of concurrent and adjuvant chemotherapy with cisplatin and docetaxel for local advanced cervical cancer. It was expected that the 3 year disease free survival would be increased by 10% with this new treatment schedule.

NCT ID: NCT02642471 Recruiting - Quality of Life Clinical Trials

Sentinel Lymph Node Biopsy Versus Pelvic Lymphadenectomy in Early-stage Cervical Cancer (PHENIX/CSEM 010)

Start date: December 2015
Phase: N/A
Study type: Interventional

The diagnostic value of sentinel lymph node biopsy in early-stage cervical cancer has been well studied. However, there were no randomized controlled study on comparing the long-term outcomes of sentinel lymph node biopsy and conventional procedure. The investigators perform a phase III, randomized controlled trial to determine whether pelvic lymphadenectomy can be replaced by sentinel lymph node biopsy in surgical treatment for patients with early-stage cervical cancer.

NCT ID: NCT02629718 Recruiting - Quality of Life Clinical Trials

Neoadjuvant Chemotherapy + Surgery Versus Surgery in FIGO IB2 and IIA2 Cervical Cancer

SYSGO-003
Start date: December 2015
Phase: Phase 3
Study type: Interventional

To clarify the potential benefits of NACT before radical surgery(RS), we perform a phase III, randomised controlled trial to compare NACT plus RS with RS alone in patients with stages IB2 and IIA2 cervical cancer.

NCT ID: NCT02624531 Recruiting - Cervical Cancer Clinical Trials

Prospective Study of Fertility-sparing Treatment Strategy in Patients With Early Cervical Cancer(SYSUGO-005/CSEM009)

SYSUGO-005
Start date: November 2015
Phase: N/A
Study type: Interventional

Patients with cervical cancer staging IB1-IIA2 desiring keeping their fertility function will be recruited. Before treatment, MRI scanning will be used to exclude retroperitoneal lymph node metastasis, involvement of lower part of uterus and endometrial carcinoma.If there is no macroscopic tumor and no obvious disease in MRI,simple trachelectomy (ST) + sentinel lymph node biopsy (SLNB) / retroperitoneal lymph node dissection(RPLND) will be performed. Otherwise,two to three cycles of neoadjuvant chemotherapy (NACT) will be administrated and then different fertility-sparing surgery(conization,ST or radical trachelectomy(RT) + SLNB/RPLND) will be employed depending on the tumor size.

NCT ID: NCT02605941 Recruiting - Cervical Cancer Clinical Trials

DNA Methylation Biomarkers for Cervical Cancer Screening

Start date: February 2014
Phase: N/A
Study type: Observational

The purpose of this prospective study is to evaluate whether DNA methylation can be applied in cervical cancer screening.

NCT ID: NCT02595554 Recruiting - Clinical trials for Cervical Carcinoma Stage IIB

Neoadjuvant Chemotherapy and Radical Surgery in Stage IIB Cervical Cancer

SYSGO002
Start date: November 2015
Phase: Phase 3
Study type: Interventional

Neoadjuvant chemotherapy (NACT) and radical surgery (RS) may have a possible better outcome to concurrent chemoirradiation (CCRT) in stage IIB cervical cancer. We try to verify such a hypothesis in terms of survival and treatment related morbidity.

NCT ID: NCT02576262 Recruiting - Cervical Cancer Clinical Trials

HPV Integration Testing for Human Papillomavirus-Positive Women

Start date: September 2015
Phase: N/A
Study type: Observational

Papanicolaou (Pap) triage, with high specificity, has been recommended for primary Human papillomavirus (HPV) testing but is flawed by poor sensitivity and cytologist dependence. the investigators evaluated the potential role of HPV Integration detection in cervical exfoliated cells in HPV-positive women from a clinic-based population.

NCT ID: NCT02576158 Recruiting - Cervical Cancer Clinical Trials

HPV Integration Testing for Cervical Cancer Screening

Start date: April 2015
Phase: N/A
Study type: Observational

The primary objective is to determine the sensitivity and specificity of the HPV Integration-based cervical screening for detection of high-grade cervical intraepithelial neoplasia (CIN), using colposcopic inspection as the reference method. Lesions will be confirmed as malignant or CIN by colposcopic inspection and histopathologic examination.

NCT ID: NCT02510027 Recruiting - Cervical Cancer Clinical Trials

Triage Strategies in Cervical Cancer Prevention

FRIDA
Start date: August 2013
Phase: N/A
Study type: Observational

While there is broad consensus that HR-HPV detection is the best available primary screening test, there is no agreement about the most efficient and reliable triage procedure for HR-HPV positive women. Transient HR-HPV infections are very common, and the vast majority of these infections spontaneously regress after a year or two. Only a small fraction of cases will lead to persistent infection responsible for cervical neoplasia. The FRIDA Study is a large, population-based study that was designed to evaluate the performance and cost-effectiveness of different triage strategies for hrHPV-positive women in Mexico.