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NCT ID: NCT01792973 Completed - Cervical Cancer Clinical Trials

HPV Infection and Cervical Lesions in HIV Infected Women in Thailand: A Prospective Study

PapilloV
Start date: February 2012
Phase:
Study type: Observational

HIV-infected women are at high risk of developing cervical cancer. This is a 3-year cohort study nested in the already existing Program for HIV Prevention and Treatment (PHPT) cohort of HIV-infected patients in Thailand (NCT 00433030). The main objective is to assess the prevalence, incidence, and clearance rate of HPV cervical infection and associated cervical lesion. The study will also provide the distribution of the HPV genotypes involved as well as other risk factors of cervical lesions. HIV-infected women receiving antiretrovirals, older than18 years of age, followed in the PHPT cohort or in the same hospitals are proposed to participate. An annual gynecological examination with a Pap-smear and a sampling for HPV testing is performed. Women with abnormal Pap-smear or with High-Risk HPV (HR-HPV) infection receive a more intensive follow-up with a colposcopy and a biopsy if necessary. Treatment is provided according to the National Guidelines.

NCT ID: NCT01791712 Completed - Sepsis Clinical Trials

Efficacy of Online Hemodiafiltrationlysis in Cytokine Removal

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

Following the concept of "peak concentration hypothesis", which suggest the cutting peak of pro- and anti-inflammatory mediators would result in restoring a situation of immunohomeostasis. The investigators conducted the prospective randomized controlled trial aimed to compare the clearance efficacy between on-line hemodiafiltration and high-flux hemodialysis in sepsis-related acute kidney injury patients. The lowering cytokines level during sepsis is postulated to improved outcomes in sepsis.

NCT ID: NCT01791413 Completed - Endometriosis Clinical Trials

Effect of Pre-operative Depo Medroxyprogesterone Acetate on Serum Anti-mullerian Hormone Level After Laparoscopic Ovarian Cystectomy of Endometriomas

Start date: March 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the ovarian reserve changes after preoperative depot medroxyprogesterone acetate (DMPA) in women with ovarian endometrioma undergoing laparoscopic cystectomy.

NCT ID: NCT01789281 Completed - Neoplasms Clinical Trials

Everolimus Roll-over Protocol for Patients Who Have Completed a Previous Novartis-sponsored Everolimus Study.

Start date: May 14, 2013
Phase: Phase 4
Study type: Interventional

Study to allow access to everolimus for patients who are on everolimus treatment in a Novartis-sponsored study and are benefiting from the treatment as judged by the investigator

NCT ID: NCT01788891 Completed - Clinical trials for Treatment Failure of Second-line ART in Asian HIV-infected Children

Second-line Therapy

TASER-P
Start date: January 2011
Phase: N/A
Study type: Observational

This study will help identify which ARV candidates should be prioritized for pediatric use in resource-limited settings

NCT ID: NCT01788852 Completed - HPV Infection Clinical Trials

HPV in Adolescents

Start date: December 2010
Phase: N/A
Study type: Observational

This study will assess the prevalence of HPV infection in perinatally HIV-infected adolescents, intraepithelial neoplasia, and E6E7 biomarker at cervical and anal sites.

NCT ID: NCT01788163 Completed - Clinical trials for EGFR Mutation Status in aNSCLC Patients

Asia Pacific and Russia Diagnostic Study for EGFR Testing

IGNITE
Start date: February 27, 2013
Phase: N/A
Study type: Interventional

Interventional diagnostic, international, multicenter and non-comparative study of EGFR mutation status in aNSCLC patients (locally advanced and/or metastatic disease) with adenocarcinoma and non-adenocarcinoma histologies. It will be conducted in Asia Pacific and Russia and will assess the current status of EGFR mutation testing, and the concordance of EGFR mutation status derived from tumour samples and blood based circulating free DNA.

NCT ID: NCT01785641 Completed - Peritonitis Clinical Trials

Single Versus Combined Antibiotic Therapy for Bacterial Peritonitis in CAPD Patients

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

To compare the efficacy of single versus combined antibiotic therapy for bacterial peritonitis in CAPD patients.

NCT ID: NCT01785472 Completed - Clinical trials for Essential Hypertension

Efficacy and Safety of LCZ696 in Comparison to Olmesartan in Asian Patients With Essential Hypertension

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

This study will assess the efficacy and safety of multiple doses of LCZ696 compared to olmesartan in Asian patients with essential hypertension

NCT ID: NCT01783444 Completed - Breast Cancer Clinical Trials

A Phase II Study of Everolimus in Combination With Exemestane Versus Everolimus Alone Versus Capecitabine in Advance Breast Cancer.

BOLERO-6
Start date: February 26, 2013
Phase: Phase 2
Study type: Interventional

This was a three-arm, randomized, open label, multi-center phase II study investigating the combination of everolimus (10mg daily) with exemestane (25mg daily) versus everolimus (10mg daily) versus capecitabine (1250mg/m2 twice daily for 14 days, 3-week cycle) in patients with estrogen-receptor positive, HER2 negative, advanced breast cancer after recurrence or progression on letrozole or anastrozole.