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Uterine Cervical Neoplasms clinical trials

View clinical trials related to Uterine Cervical Neoplasms.

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NCT ID: NCT05511740 Completed - Cervical Cancer Clinical Trials

Circadian as A Prognostic Factor For Radiation Response in Cervical Cancer

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

The study was a Randomized Clinical Trial (RCT) or clinical trial comparing the results of radiation treatment of 2 treatment groups, i.e. subject groups irradiated in the morning and in the afternoon, to check melatonin levels in cervical cancer patients. Since it is known that the function of melatonin is as an antiproliferation substance or hormone, induces apoptosis, inhibits invasion and metastasis.

NCT ID: NCT05511623 Recruiting - Cervical Cancer Clinical Trials

Tislelizumab Combined With Concurrent Chemoradiotherapy as First-line Treatment for Stage IIIC2 Cervical Cancer

Start date: September 1, 2022
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy and safety of tislelizumab combined with concurrent chemoradiotherapy in first-line treatment of stage IIIC2 cervical cancer.

NCT ID: NCT05504642 Withdrawn - Clinical trials for Cervical Cancer = FIGO IIB and or Lymph Node Metastases

Chemo-radio-immunotherapy With Nivolumab and Ipilimumab Treatment in Locally Advanced Cervical Cancer Patients

CERAD-IMMUNE
Start date: November 1, 2023
Phase: Phase 2
Study type: Interventional

The purpose of this study is to use Chemo-radio-immunotherapy and maintenance therapy with Nivolumab and Ipilimumab in order to achieve improved outcome in patients with locally advanced cervical cancer.

NCT ID: NCT05492123 Recruiting - Clinical trials for Uterine Cervical Neoplasms

Nivolumab-ipilimumab and Chemoradiation for Cervical Cancer

Start date: August 30, 2022
Phase: Phase 2
Study type: Interventional

A total of 112 patients with locally advanced cervical cancer will be randomized 1:1 to standard therapy with cisplatin-based chemoradiation or nivolumab-ipilimumab induction followed by cisplatin-based chemoradiation. The primary outcome will be 3-year disease-free survival.

NCT ID: NCT05489978 Completed - Cervical Cancer Clinical Trials

Effectiveness of a Cervical Cancer Stigma Reduction Intervention Program on Cancer Stigma Score and Cervical Cancer Screening Uptake in Nepal

Start date: June 15, 2022
Phase: N/A
Study type: Interventional

It is a cluster randomized control trial to assess the effectiveness of the cervical cancer stigma reduction intervention on cancer stigma score and cervical cancer screening uptake in Nepal

NCT ID: NCT05483491 Recruiting - Breast Cancer Clinical Trials

KK-LC-1 TCR-T Cell Therapy for Gastric, Breast, Cervical, and Lung Cancer

Start date: September 26, 2022
Phase: Phase 1
Study type: Interventional

This is a phase I clinical trial to determine the maximum tolerated dose (MTD) of KK-LC-1 TCR-T cells for the treatment of metastatic cancers that express KK-LC-1. Participants will receive a conditioning regimen, KK-LC-1 TCR-T cells, and aldesleukin. The safety profile and clinical response to treatment will be determined.

NCT ID: NCT05475847 Recruiting - Cervical Cancer Clinical Trials

Study of C-TIL052A Cell Therapy in Advanced Cervical Cancer

TIL
Start date: July 2022
Phase: Phase 1
Study type: Interventional

A study that aimed to assess the safety and anti-tumor activity of C-TIL052A cell therapy in subjects with persistent, recurrent and/or metastatic cervical cancer.

NCT ID: NCT05475171 Recruiting - Cervical Cancer Clinical Trials

Triage of Advanced Cervical Cancer Through Immunotherapy Induction (TRACTION)

Start date: December 13, 2022
Phase: Phase 2
Study type: Interventional

To learn if MGD019 can help to control cervical cancer in patients who have yet to receive treatment.

NCT ID: NCT05474404 Recruiting - Cervical Cancer Clinical Trials

Telecytology as a Triage Tool in LMICs

Start date: April 25, 2022
Phase:
Study type: Observational

The investigators will collect PAP-test samples from women undergoing colposcopy. Laboratory providers will prepare the samples with a liquid-based cytology method. The providers will then digitalise the slides using a digital scanner. The slides will be sent to cytopathologists who will assess the quality of the slides.

NCT ID: NCT05472311 Recruiting - Cervical Cancer Clinical Trials

Cervical Cancer Elimination -Using Implementation Science to Evaluate Deliver and Cost Introduction of Thermal Ablation

TIBA
Start date: May 17, 2022
Phase: N/A
Study type: Interventional

Global elimination of cervical cancer is a feasible goal; however, the countries with the greatest disease burden also have the greatest healthcare system challenges. Cervical cancer (CC) is almost entirely preventable, yet, it remains the 2nd most common cause of cancer and is the most common cause of cancer deaths among women in the majority of Low-Middle-Income-Countries (LMIC) including Kenya. Effective low-cost interventions for early detection of pre-cancer lesions have been available but there remains very low coverage with about 16% eligible women screened in Kenya. Cryotherapy has been introduced as a low-cost intervention for treatment of pre-cancer lesions, however, challenges with equipment shortage, costs, supply chain difficulties of refrigerant gas and equipment failure health facilities has been cited as a reason for the low treatment rates of screen positive women. In Kenya only about 30% of women screening positive access treatment for the pre-cancer lesions. This project will introduce thermal ablation (TA), which is proven to be safe and as effective as cryotherapy for treatment of pre-cancer lesions of the cervix. TA uses electricity, batteries or solar to charge, takes a shorter time to use, is a small easily portable equipment. The primary aim of the study is to deliver, evaluate and cost implementation of the 'Single Visit Screen and Treat with Thermal Ablation' (SVA-SAT+TA) intervention for treatment of women who screen positive for pre-cancer lesions of the cervix in reproductive health clinics in Kenya, using implementation science framework to inform National scale-up. To achieve national and global goals to eliminate cervical cancer, there is an urgent need to adapt, implement, and scale-up effective technologies in Kenya. The proposed research project will develop a contextually appropriate implementation and dissemination model to guide effective scale-up of the single visit screen and treat approach with use of thermal ablation to health facilities to bridge access to cervical cancer prevention services for women in Kenya and similar low resource settings.