Clinical Trials on GLENOID CAVITY

Total 944 results

Olubukola Nafiu

Not yet recruiting

Metabolomic Profiling of Racial Disparity

Surgery | Tonsillar Hypertrophy | Adenoid Hypertrophy
Gustave Roussy, Cancer Campus, Grand Paris

Unknown

Study of Imatinib (Glivec) in Patients With Adenoid Cystic Carcinoma of the Head and Neck

Carcinoma, Adenoid Cystic | Cancer of the Head and Neck

France
Alpha Tau Medical LTD.

Recruiting

Retreatment With Intratumoral Diffusing Alpha Radiation Emitters

Skin Cancer | Mucosal Neoplasm of Oral Cavity | Soft Tissue Neoplasm

Israel
Case Comprehensive Cancer Center
National Cancer Institute (NCI)

Terminated

Stereotactic Body Radiation Therapy in Treating Patients With High Risk Locally Advanced Head and Neck Cancer

Recurrent Hypopharyngeal Squamous Cell Carcinoma | Recurrent Laryngeal Squamous Cell Carcinoma | Recurrent Oral Cavity Squamous Cell Carcinoma | Recurrent Oropharyngeal Squamous Cell Carcinoma | Recurrent Nasopharyngeal Keratinizing Squamous Cell Carcinoma | Stage IVA Oral Cavity Squamous Cell... and other conditions

United States
National Cancer Institute (NCI)

Terminated

Capecitabine and Vorinostat in Treating Patients With Recurrent and/or Metastatic Head and Neck Cancer

Recurrent Hypopharyngeal Squamous Cell Carcinoma | Recurrent Laryngeal Squamous Cell Carcinoma | Recurrent Oral Cavity Squamous Cell Carcinoma | Recurrent Oropharyngeal Squamous Cell Carcinoma | Stage IVA Oral Cavity Squamous Cell Carcinoma | Stage IVA Laryngeal Squamous Cell Carcinoma | Stage... and other conditions

Canada, United States
Sichuan University

Recruiting

Dual-targeting VEGFR1 and PD-L1 CAR-T for Cancers Patients With Pleural or Peritoneal Metastases

Malignant Ascites | Malignant Peritoneal Effusion | Serous Cavity Metastatises

China
Gynecologic Oncology Group
National Cancer Institute (NCI)

Terminated

Combination Chemotherapy in Treating Patients With Previously Untreated Stage III or Stage IV Ovarian or Primary Peritoneal Cancer

Ovarian Cancer | Primary Peritoneal Cavity Cancer

United States, Canada
Emory University
Synta Pharmaceuticals Corp.

Terminated

Ganetespib Window of Opportunity Study in Head and Neck Cancers

Stage IVA Oral Cavity Squamous Cell Carcinoma | Stage IVA Laryngeal Squamous Cell Carcinoma | Stage IVA Oropharyngeal Squamous Cell Carcinoma | Stage I Hypopharyngeal Squamous Cell Carcinoma | Stage I Laryngeal Squamous Cell Carcinoma | Stage I Oropharyngeal Squamous Cell Carcinoma | Stage II... and other conditions

United States
Alpha Tau Medical LTD.

Recruiting

Alpha Radiation Emitters Device (DaRT) for the Treatment of Cutaneous, Mucosal or Superficial Soft Tissue Neoplasia

Skin Cancer | Mucosal Neoplasm of Oral Cavity | Soft Tissue Neoplasm

Israel
Alpha Tau Medical LTD.

Recruiting

Alpha Radiation Emitters Device (DaRT) for the Treatment of Cutaneous, Mucosal or Superficial Soft Tissue Neoplasia.

Skin Cancer | Mucosal Neoplasm of Oral Cavity | Soft Tissue Neoplasm

Israel
Nationwide Children's Hospital
Zotarix LLC

Enrolling by invitation

Oral Device Clinical Trial

Dental Diseases | Tonsil Disease | Adenoid; Disorder (and Tonsils)

United States
Shanghai Ninth People's Hospital Affiliated to...
Fudan University

Completed

Postoperative CCRT With Docetaxel vs Cisplatin in High Risk Oral Cavity Cancer

Oral Cavity Squamous Cell Carcinoma

China
Fondazione IRCCS Istituto Nazionale dei Tumori,...

Completed

Lenvatinib in Recurrent and/or Metastatic Adenoid Cystic Carcinomas of the Salivary Glands: ACC-LEN14 (ACC-LEN14)

Adenoid Cystic Carcinomas of the Salivary Glands

Italy
Alcon Research
Queensland University of Technology

Recruiting

Post-Market Study of Alcon Intraocular Lenses

Visual Acuity

Australia
Johnson & Johnson Vision Care, Inc.

Completed

The Effects of Contact Lenses With UV/HEV-Filter on Visual Function

Visual Acuity

United States
Alcon Research

Completed

Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal IOL

Visual Acuity

United States
Johnson & Johnson Vision Care, Inc.

Completed

Clinical Evaluation of an Investigational Lipid Drop in Non-contact Lens Wearing Patients

Visual Acuity

United States
Johnson & Johnson Vision Care, Inc.

Completed

Clinical Performance of Senofilcon A Investigational Lens

Visual Acuity

United States
Johnson & Johnson Vision Care, Inc.

Completed

Clinical Investigation of Visual Acuity in Contact Lens Wearers After Instillation of Investigational Lubricating Eye Drops

Visual Acuity

United States
Johnson & Johnson Vision Care, Inc.

Completed

Comparison of a Silicone Hydrogel Daily Disposable Multifocal Contact Lens to a Marketed Product

Visual Acuity

United States
Johnson & Johnson Vision Care, Inc.

Completed

Validation of Senofilcon A With New UV / HEV Filter

Visual Acuity

United States
Johnson & Johnson Vision Care, Inc.

Completed

Evaluation of Visual Acuity With a Reusable Toric Multifocal Contact Lens

Visual Acuity

United States
Johnson & Johnson Vision Care, Inc.

Completed

Evaluation of Comfort for Two Marketed Daily Disposable Contact Lenses

Visual Acuity

United States
Johnson & Johnson Vision Care, Inc.

Completed

Evaluation of Investigational Daily Disposable Multifocal Contact Lenses Produced With Different Manufacturing Processes

Visual Acuity

United States
Johnson & Johnson Vision Care, Inc.

Completed

Clinical Evaluation of Etafilcon A With Ketotifen

Visual Acuity

United States
Johnson & Johnson Vision Care, Inc.

Completed

Clinical Evaluation of Daily Disposable Etafilcon A Cosmetic Contact Lenses

Visual Acuity

United States, Hong Kong
Johnson & Johnson Vision Care, Inc.

Completed

Dynamic Characterisation of Meibomian Gland Structure

Visual Acuity

United Kingdom
Johnson & Johnson Vision Care, Inc.

Completed

Objective Vision Evaluation of Two Cosmetic Contact Lenses

Visual Acuity

United States
Johnson & Johnson Vision Care, Inc.

Completed

Ocular Characteristics in Contact Lens and Spectacle Wear

Visual Acuity

United States
The University of Hong Kong

Completed

Evaluation of Letters Versus Numbers (ELEVEN) Study (ELEVEN)

Visual Acuity

Hong Kong
Johnson & Johnson Vision Care, Inc.

Completed

Clinical Evaluation of Manufacturing Processes for a Reusable Multifocal Optical Design in a Presbyopic Population

Visual Acuity

United States
Johnson & Johnson Vision Care, Inc.

Completed

An Investigation of the Impact of Localized Topical Anesthesia of the Ocular Surface on End-of-day Contact Lens Discomfort

Visual Acuity

United Kingdom
Seoul National University Hospital

Completed

Effect of Vaginal Radiofrequency Therapy on Vaginal Laxity : Pilot Trial (ROSE)

Vaginal Laxity

Korea, Republic of
University Clinic Frankfurt

Completed

To Evaluate the Visual Performance After Bilateral Implantation of Multifocal Intraocular Lenses

Visual Acuity

Germany
Johnson & Johnson Vision Care, Inc.

Completed

Clinical Evaluation of 2-Week Reusable ACUVUE 2 Vivid Style

Visual Acuity

United States
Johnson & Johnson Vision Care, Inc.

Completed

Evaluation of Approved and Investigational Contact Lenses

Visual Acuity

United States
Johnson & Johnson Vision Care, Inc.

Completed

Clinical Performance Evaluation of Two Silicone Hydrogel Lenses

Visual Acuity

Canada
Johnson & Johnson Vision Care, Inc.

Completed

Clinical and Laboratory Study of Lysozyme Deposition on Daily Disposable Contact Lenses

Visual Acuity

Canada
Poitiers University Hospital

Completed

Physiological Upper Eyelid Laxity (LAX)

Eyelid Laxity

France
Johnson & Johnson Vision Care, Inc.

Completed

Evaluation of Three Daily Disposable Contact Lenses

Visual Acuity

Canada
Syneron Medical

Unknown

Treatment With the Profound System for Submental Laxity

Submental Laxity

United States
University of Pennsylvania
Carnegie Mellon University

Completed

Using Technology to Promote Mental Acuity

Mental Acuity

United States
Hospital Oftalmologico de Brasilia
Federal University of Minas Gerais

Completed

Transconjunctival Sutureless 25-Gauge Vitrectomy (TSV-25G)

Visual Acuity

Brazil
University of Washington
National Cancer Institute (NCI)

Completed

TLR8 Agonist VTX-2337 and Cetuximab in Treating Patients With Locally Advanced, Recurrent, or Metastatic Squamous Cell Cancer of Head and Neck

Tongue Cancer | Recurrent Metastatic Squamous Neck Cancer With Occult Primary | Recurrent Salivary Gland Cancer | Recurrent Squamous Cell Carcinoma of the Hypopharynx | Recurrent Squamous Cell Carcinoma of the Larynx | Recurrent Squamous Cell Carcinoma of the Lip and Oral Cavity | Recurrent Squamous... and other conditions

United States
Wake Forest University Health Sciences
National Cancer Institute (NCI)

Completed

Prepare to Care, A Supported Self-Management Intervention for Head and Neck Cancer CaregiversHead and Neck Cancer

Recurrent Head and Neck Squamous Cell Carcinoma | Recurrent Hypopharyngeal Squamous Cell Carcinoma | Recurrent Laryngeal Squamous Cell Carcinoma | Caregiver | Salivary Gland Squamous Cell Carcinoma | Malignant Head and Neck Neoplasm | Recurrent Lip and Oral Cavity Squamous Cell Carcinoma | Stage... and other conditions

United States
National Cancer Institute (NCI)

Withdrawn

Nivolumab or Expectant Observation Following Ipilimumab, Nivolumab, and Surgery in Treating Patients With High Risk Localized, Locoregionally Advanced, or Recurrent Mucosal Melanoma

Cervical Carcinoma | Recurrent Melanoma | Vaginal Carcinoma | Esophageal Carcinoma | Mucosal Melanoma | Mucosal Melanoma of the Head and Neck | Oral Cavity Mucosal Melanoma | Stage II Vulvar Cancer AJCC v7 | Stage III Vulvar Cancer AJCC v7 | Stage IIIA Vulvar Cancer AJCC v7 | Stage IIIB Vulvar Cancer AJCC v7 and other conditions

United States
M.D. Anderson Cancer Center
National Cancer Institute (NCI)

Active, not recruiting

Multimodal Imaging for Surveillance in Patients With Oral Potentially Malignant Disorders

Dysplasia | Premalignant Lesion | Lip and Oral Cavity Carcinoma | Oral Disorder

United States
M.D. Anderson Cancer Center
National Cancer Institute (NCI)

Active, not recruiting

Pembrolizumab in Treating Patients With High Risk Oral Intraepithelial Neoplasia

Oral Cavity Carcinoma | Oral Intraepithelial Neoplasia

United States
Merck Sharp & Dohme LLC

Terminated

Paclitaxel Plus Carboplatin With or Without SCH-58500 in Treating Patients With Newly Diagnosed Stage III Ovarian or Stage III Primary Peritoneal Cancer

Ovarian Cancer | Primary Peritoneal Cavity Cancer
Rhode Island Hospital

Completed

Lidocaine Infusion for Pain Relief in Children Scheduled for Tonsillectomy and Adenoidectomy

Children, Only | Tonsillar Hypertrophy | Adenoid Hypertrophy

United States

Clinical Trials on GLENOID CAVITY

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