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Basal Cell Carcinoma clinical trials

View clinical trials related to Basal Cell Carcinoma.

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NCT ID: NCT00988455 Completed - Clinical trials for Basal Cell Carcinoma

Evaluation of Efficacy of Photodynamic Therapy in Basal Cell Carcinoma With 6 Months Follow-up

Start date: January 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy of photodynamic therapy (PDT)in treatment of Basal cell carcinoma (BCC) and recurrence rate after 6 months.

NCT ID: NCT00985829 Completed - Clinical trials for Basal Cell Carcinoma

Evaluation of Efficacy of Photodynamic Therapy in Basal Cell Carcinoma

Start date: January 2008
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the efficacy of pdt in treatment of bcc and factors that affect response rate.

NCT ID: NCT00959647 Completed - Ovarian Cancer Clinical Trials

A Study of Vismodegib (GDC-0449) in Patients Treated With Vismodegib in a Previous Genentech-sponsored Phase I or II Cancer Study

Start date: September 2009
Phase: Phase 2
Study type: Interventional

This was a multicenter, open-label extension study. Patients who received vismodegib (GDC-0449) in a Genentech-sponsored study and who had completed the parent study or who continued to receive vismodegib at the time the parent study closed were eligible for continued treatment in this protocol.

NCT ID: NCT00882791 Completed - Clinical trials for Basal Cell Carcinoma

Basal Cell Carcinoma Recurrence After Mohs Surgery

Start date: May 2008
Phase:
Study type: Observational

Basal cell carcinoma (BCC) is the most common skin cancer in the US and can cause significant adverse effects. Mohs micrographic surgery, the treatment of choice for higher risk BCC, allows for removal of lesions with preservation of healthy tissue. Although the BCC recurrence rate post Mohs surgery is estimated at 1-2%, recent data is lacking to validate this historical measurement. Our purpose is to determine the current recurrence rate of BCC after Mohs surgery.

NCT ID: NCT00880308 Completed - Clinical trials for Basal Cell Carcinoma

Dose Finding and Safety of Oral LDE225 in Patients With Advanced Solid Tumors

Start date: March 2009
Phase: Phase 1
Study type: Interventional

This first-in-human dose-escalation study is to characterize the safety, tolerability, pharmacokinetics and pharmacodynamics of LDE225 given orally on a daily dosing schedule in patients with advanced solid tumors.

NCT ID: NCT00836342 Completed - Clinical trials for Squamous Cell Carcinoma

Correlation Between Skin Carotenoid Levels and Previous History of Skin Cancer

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

The purpose of this study is to determine the difference of skin carotenoid levels between subjects with previous squamous cell carcinomas (SCC), subjects with previous basal cell carcinomas (BCC) and a control group.

NCT ID: NCT00833417 Completed - Clinical trials for Basal Cell Carcinoma

A Study Evaluating the Efficacy and Safety of Vismodegib (GDC-0449, Hedgehog Pathway Inhibitor) in Patients With Advanced Basal Cell Carcinoma

Start date: February 2009
Phase: Phase 2
Study type: Interventional

This was a Phase II, single-arm, two-cohort multicenter clinical trial evaluating the efficacy and safety of vismodegib (GDC-0449) in patients with advanced basal cell carcinoma. All patients received vismodegib until evidence of progression, intolerable toxicities most probably attributable to vismodegib, or withdrawal from the study.

NCT ID: NCT00793169 Completed - Clinical trials for Squamous Cell Carcinoma

Serum Concentration of Lidocaine After Local Injection During Mohs Micrographic Surgery

Start date: September 2007
Phase:
Study type: Observational

The primary objective of this study is to (1) determine whether local injection of lidocaine used during Mohs surgery will elevate serum lidocaine concentrations to a level that could cause systemic symptoms and (2) determine whether sustained high levels of serum lidocaine occur after intralesional anesthesia on the face and neck. This study is a cross-sectional study of 10 subjects with basal cell carcinoma or squamous cell carcinoma of the face or neck requiring Mohs micrographic surgery. The study will consist of a brief questionnaire and blood draws during their Moh's surgical procedure.

NCT ID: NCT00765193 Completed - Melanoma Clinical Trials

The Impact of Total Body Skin Examination on Skin Cancer Detection

TBSE
Start date: May 2008
Phase: N/A
Study type: Interventional

This will be a study where all patients will undergo a two-step procedure: Step 1 - Physicians examine the problem area of skin ONLY and record result. Step 2 - Physicians perform TBSE and record result. Eventual lesions suggestive of melanoma and non-melanoma skin cancers will be recorded after step 1 or step 2 examination and will be finally biopsied and histopathologically diagnosed. Exceptions to biopsy may include patients with multiple non-melanoma skin cancers (e.g. actinic keratoses or basal cell carcinomas). Each center will be provided with an electronic data sheet for patients record, or alternatively, with a paper record form. Endpoints of the study are new parameters concerning the standard of care for skin cancer screening. We expect to conclude that TBSE enables clinicians discovering an increased number of skin cancers thus resulting in earlier detection.

NCT ID: NCT00663650 Recruiting - Clinical trials for Basal Cell Carcinoma

Periocular Basal Cell Carcinoma (BCC): Permanent vs. Frozen Section Pathological Control

Start date: August 2008
Phase: Phase 3
Study type: Interventional

This study is an equivalency study designed as a randomized clinical trial. Patients with a biopsy proven nodular periocular basal cell carcinoma (BCC) who have agreed to have surgical excision will be eligible. Study patients will undergo surgical excision of the lesion and then be randomized to having frozen section or permanent section pathological control. For those patients randomized to permanent section control the sample will be sent to pathology and surgical reconstruction will be performed. Patients randomized to frozen section will have additional margins re-excised before reconstruction depending on the pathologic results. Tumor clearance rates after surgical excision will be compared between the two techniques as a primary study question. Patients will be followed long-term to determine recurrence rates in the two groups. The study is designed to determine if the two techniques are equivalent within a given margin of error with respect to outcome measures.