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Carcinoma in Situ clinical trials

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NCT ID: NCT01298596 Completed - Clinical trials for Cervical Intraepithelial Neoplasia

Cryotherapy vs. LEEP to Treat Cervical Intraepithelial Neoplasia (CIN) 2/3 Among HIV-positive Women

PHE-LEEP
Start date: June 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the rate of recurrence of cervical intraepithelial neoplasia among HIV-positive women receiving cryotherapy versus LEEP over 2 years of follow-up and to compare the shedding of HIV-1 from the cervix between HIV-positive women receiving cryotherapy versus LEEP over 3 weeks of follow-up.

NCT ID: NCT01259063 Completed - Bladder Cancer Clinical Trials

RAD001 and Intravesical Gemcitabine in BCG-Refractory Primary or Secondary Carcinoma In Situ of the Bladder

Start date: December 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to test the safety of gemcitabine applied to the bladder directly combined with different oral doses of everolimus and to assess the right doses. Gemcitabine will be given at a fixed dose. Up to 3 dose levels of everolimus will be evaluated. The purpose of the phase II part is to test the combination of gemcitabine applied to the bladder directly combined with different oral doses of everolimus and to study the effects of these two drugs together. The investigators want to find out what effects, good and/or bad, this treatment has on the patient and the cancer.

NCT ID: NCT01256424 Completed - Clinical trials for Cervical Intraepithelial Neoplasia

Dose-finding Study of Hexaminolevulinate (HAL) Photodynamic Therapy (PDT) to Treat Cervical Neoplasia

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

An effective and safe medical therapy would be most welcome to reduce the need for surgical interventions and related adverse events and psychological impact on patients with cervical cancer precursors. In this clinical trial, the investigators propose to evaluate the efficacy and safety of photodynamic therapy (PDT) using hexaminolevulinate (HAL) for mild to moderate-grade CIN (grade 1-2).

NCT ID: NCT01245972 Completed - Clinical trials for Basal Cell Carcinoma

Pilot Study of PDL to Treat BCC and SCCIS

PDLNMSC
Start date: August 2010
Phase: N/A
Study type: Interventional

This is a research study to find out more about the use of the pulsed dye laser in the treatment of basal cell carcinoma and early stage squamous cell carcinoma that has not invaded deep into the skin. The purpose of this study is to determine whether the use of the pulsed dye laser (PDL) can completely clear or regress basal cell carcinoma or early stage squamous cell carcinoma. Pulsed dye laser is a type of laser that is commonly used to treat lesions on the skin that have a prominent blood vessel component. It has been used to treat broken blood vessels on the face, hemangiomas in children and adults, leg veins, port wine stains, and other lesions with a prominent vascular component.

NCT ID: NCT01219075 Completed - Clinical trials for Stage IIIA Breast Cancer

Soy Isoflavones Supplementation in Treating Women at High Risk For or With Breast Cancer

Start date: July 1, 2010
Phase: N/A
Study type: Interventional

RATIONALE: Chemoprevention is the use of certain drugs to keep cancer from forming. The use of soy isoflavones supplements may prevent or treat early stage breast cancer. PURPOSE: This clinical trial studies soy isoflavones supplementation in treating women at high risk for or with breast cancer.

NCT ID: NCT01194440 Completed - Clinical trials for Stage IIIA Breast Cancer

Zoledronic Acid in Aromatase Inhibitor Induced Musculoskeletal Symptoms

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

RATIONALE: Zoledronic acid may prevent bone loss and help prevent or lessen musculoskeletal symptoms in women receiving hormone therapy for breast cancer. PURPOSE: This phase II trial is studying how well zoledronic acid works in preventing musculoskeletal symptoms in post-menopausal women with stage I, stage II, or stage III breast cancer receiving letrozole.

NCT ID: NCT01192204 Completed - Clinical trials for Intraepithelial Neoplasia

Clinical Evaluation of Bioadhesive Gels for Oral Cancer Chemoprevention

Start date: October 2010
Phase: Phase 1/Phase 2
Study type: Interventional

This is a multicenter placebo-controlled clinical trial to assess the effects of a topically applied gel on precancerous oral epithelial lesions. A total of 41 participants will be enrolled in this trial, and 22 of them will be enrolled at Ohio State. [The remaining 19 participants will be enrolled at the University of North Carolina (9 participants) and the University of Louisville (8 participants)]. At all three institutions, half of the participants will randomly be assigned to the 10% FBR gel (0.5 gm four times daily for 3 months), while half will enter the placebo control arm. All trial participants will have a pretreatment (including lesional and perilesional tissue) biopsy taken before and an excisional biopsy after 3 months of treatment. As pretreatment indices are compared to post treatment effects on each patient, patients serve as their own internal control. Pretreatment lesional biopsies are obtained to establish a pretreatment diagnosis and provide a pretreatment baseline for the experimental parameters.

NCT ID: NCT01160185 Completed - Clinical trials for Cervical Intraepithelial Neoplasia

Meta-analysis of Efficacy of Topotecan

Start date: June 2009
Phase: N/A
Study type: Observational

This meta-analysis was conducted to investigate the efficacy of Topotecan and other treatments for recurrent and stage IVB carcinoma of the cervix

NCT ID: NCT01145781 Completed - Clinical trials for Cervical Intraepithelial Neoplasia

Trial to Evaluate Single- and Double- Freeze Cryotherapy in the Prevention of Cervical Neoplasia

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

To evaluate whether single- and double-freeze cryotherapy techniques have similar efficacy in controlling different grades of cervical intraepithelial neoplasia (CIN), and have similar side effects and complications.

NCT ID: NCT01140178 Completed - Dysplasia Clinical Trials

A Trial of Photodynamic Therapy With HPPH for Treatment of Dysplasia, Carcinoma in Situ and T1 Carcinoma of the Oral Cavity and/or Oropharynx

Start date: June 8, 2010
Phase: Phase 1
Study type: Interventional

Recent literature suggests that certain patients with squamous cell cancers of the head and neck region may benefit from photodynamic therapy whether or not they may have received prior therapy, e.g. radiation therapy