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Carcinoma, Squamous Cell clinical trials

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NCT ID: NCT01770002 Completed - Melanoma Clinical Trials

Eversion in Dermatologic Surgery: Is Cosmetic Appearance Improved?

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

The investigators hypothesize that everting wound edges while suturing surgical sites will result in more aesthetic scars. Additionally, we also hypothesize that small to moderate wound irregularities present at 3 months will resolve by 6 months after surgery with no intervention

NCT ID: NCT01760811 Not yet recruiting - Clinical trials for Squamous Cell Carcinoma

CETUXIMAB Given for 3 Weeks as Neoadjuvant Treatment in Locally Advanced Tongue Cancer ; A NEW PARADIGM OF TREATMENT

Start date: January 2013
Phase: Phase 1/Phase 2
Study type: Interventional

To compare the Disease free survival (DFS) rate of a preoperative cetuximab treatment followed by operation and postoperative radiation-cisplatin-cetuximab treatment paradigm for advanced oral cavity cancer, , with the DFS rate of historical controls (from the RTOG 9501 and EORTC 22931 studies in which treatment was with surgery followed by radiotherapy and cisplatin) with a similar stage of the disease.

NCT ID: NCT01758731 Completed - Clinical trials for Squamous Cell Carcinoma of the Head and Neck

Study of Olaparib With Radiation Therapy and Cetuximab in Advanced Head and Neck Cancer With Heavy Smoking History

Start date: October 22, 2012
Phase: Phase 1
Study type: Interventional

This is a research study that plans to learn more about the safety and tolerability of an investigational drug called Olaparib, in combination with radiation therapy and cetuximab. Hypothesis: Intensity modulated radiotherapy with concurrent C225 and Olaparib represents a feasible, biologically-based alternative to standard chemoradiation, with acceptable toxicity, for treatment of locally-advanced HNSCC in patients having a ≥ 10 pack-year smoking history.

NCT ID: NCT01755650 Terminated - Clinical trials for Squamous Cell Carcinoma

Phase 0 of 18F FPM Using PET/CT in Patients With a Variety of Malignancies

Start date: October 2011
Phase: Early Phase 1
Study type: Interventional

The purpose of this study is to investigate the safety and potential effectiveness of the imaging compound 18F FPM for finding sites of malignancies.

NCT ID: NCT01752205 Recruiting - Clinical trials for Esophageal Squamous Carcinoma

Paclitaxel Plus Radiation With Erlotinib to Treat Esophageal Squamous Carcinoma

ESCC-307PLAH
Start date: November 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test the safety and effectiveness of erlotinib and chemoradiotherapy in patients with unresectable esophageal or gastro-esophageal squamous cancer .

NCT ID: NCT01748942 Completed - Pain Clinical Trials

Dexamethasone in Reducing Oral Pain and Dry Mouth After Surgery in Patients With Oropharyngeal Cancer

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

This randomized pilot clinical trial studies dexamethasone in reducing oral pain and dry mouth after surgery in patients with oropharyngeal cancer. Dexamethasone may help lower pain and dry mouth caused by surgery.

NCT ID: NCT01740375 Terminated - Clinical trials for Esophageal Squamous Cell Carcinoma

Role of Esophagectomy in Complete Responders to CCRT

ESOPRESSO
Start date: November 2012
Phase: Phase 3
Study type: Interventional

To investigate the role of esophagectomy in complete responders to preoperative chemoradiotherapy for squamous cell carcinoma of esophagus, patients will be randomized to either observation or esophagectomy after concurrent chemoradiotherapy.

NCT ID: NCT01737008 Completed - Clinical trials for Squamous Cell Carcinoma of the Head and Neck

Dacomitinib Plus Radiotherapy, With and Without Cisplatin in Patients With Squamous Cell Carcinoma of the Head and Neck

Start date: January 2013
Phase: Phase 1
Study type: Interventional

This is a phase 1 study of the drug dacomitinib with radiotherapy, with or without chemotherapy, in patients with advanced squamous cell carcinoma of the head and neck (SCCHN). Dacomitinib is an oral drug, which is found to be active in SCCHN patients, blocks a receptor called the epidermal growth factor receptor (EGFR). By blocking signals for cancer cells to grow, it is believed to stop or slow the growth of tumor cells. The dose escalation phase will find the best dose as well as determine the safety of dacomitinib when given with radiotherapy and with or without chemotherapy.The dose expansion phase will further test the best dose determined in the dose escalation phase for response rate.

NCT ID: NCT01732640 Terminated - Clinical trials for Squamous Cell Carcinoma of the Head and Neck

A Phase I/II Study Afatinib/Carboplatin/Paclitaxel Induction Chemotherapy In HPV-Negative HNSCC.

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

Trial Objectives: The objective is to investigate the efficacy and safety of afatinib with induction chemotherapy in primary unresected patients with locally advanced, HPV-negative, stage III or IVa/b HNSCC including oral cavity, oropharynx, hypopharynx, or larynx. Primary Objective Phase I The primary objective of the phase I portion of the trial is to determine the maximum tolerated dose (MTD) or the recommended phase II dose of daily oral afatinib that is safe in combination with carboplatin AUC 6 and paclitaxel 175mg/m2 q 21 days as an induction regimen. Primary Objective Phase 2 The primary objective of the phase 2 portion of the trial is to estimate the objective tumor response rate and toxicity with induction therapy in patients treated on the afatinib dose determined in Phase I. Secondary Objectives The secondary objective of phase II is to estimate: 1) the overall response to entire treatment after completion of CRT, 2) progression-free survival (PFS) rate at 2 years, and 3) overall survival (OS) at 2 years.

NCT ID: NCT01728480 Withdrawn - Mucositis Clinical Trials

Entolimod in Treating Patients With Stage III-IV Squamous Cell Head and Neck Cancer Receiving Cisplatin and Radiation Therapy

Start date: January 2014
Phase: Phase 1
Study type: Interventional

This phase I trial studies the side effects and best dose of entolimod in treating patients with stage III-IV or recurrent head and neck cancer. Biological therapies, such as entolimod, may stimulate the immune system in different ways and stop tumor cells from growing. Entolimod may also prevent side effects caused by chemotherapy with cisplatin and radiation therapy. Radiation therapy uses high-energy x-rays to kill tumor cells. Drugs used in chemotherapy, such as cisplatin, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving entolimod together with cisplatin and radiation therapy may kill more tumor cells