Search clinical trials for: Mucositis Oral

Total 17611 results

SkyePharma AG
Abbott

Completed

A Phase I Study in Asthma Patients Evaluating the Effect of Doses of FlutiForm™ on the Amount, if Any, of Cortisol Produced by the Adrenal Glands

Asthma

United States
Mansoura University

Completed

Clinical Impacts of Oral Gastrografin Follow Through in Adhesive Small Bowel Obstruction (SBO)

Small Bowel Obstruction

Egypt
Hawler Medical University
HAWLER Maternity Hospital

Completed

Misoprostol in Termination of First Trimester Missed Abortion

Miscarriage

Iraq
All India Institute of Medical Sciences, New Delhi

Completed

Effect of Addition of Oral Montelukast to Standard Treatment in Acute Moderate to Severe Asthma in Children (Montelukast)

Bronchial Asthma

India
Novartis

Completed

Safety and Efficacy of Oral PTK787 in Patients With Subfoveal Choroidal Neovascularization Secondary to Age-Related Macular Degeneration (AMD) (ADVANCE)

Wet Age-Related Macular Degeneration

Australia, United States
Shizuoka Cancer Center

Unknown

Phase I/II Study of SOL for Untreated Metastatic Colorectal Cancer

Colorectal Cancer

Japan
University of Dundee
NHS Tayside; Chief Scientist Office of the Scottish Government

Completed

Medical Polypectomy and Predictors of Response

Nasal Polyps

United Kingdom
Medical University of Vienna

Unknown

Analysis of Immunological Reactions to Foods in Birch Pollen-Allergic Patients

Allergic Rhinitis | Food Allergy
Innoventus Project AB
Uppsala University

Completed

A Safety/Tolerability and Pharmakokinetic Study of Sargramostim Administrated in the Gingiva

Periodontitis

Sweden
Ranbaxy Laboratories Limited

Completed

Bioequivalence Study of Amoxicillin-Clavulanic Acid 600 mg - 42.9 mg/ 5 mL Oral Suspension Under Fasting Conditions

Healthy

Canada
Ranbaxy Laboratories Limited

Completed

Bioequivalence Study of Amoxicillin-Clavulanic Acid 600 mg-42.9 mg/ 5 mL Oral Suspension Under Fed Conditions

Healthy

Canada
Ranbaxy Laboratories Limited

Completed

Bioequivalence Study of Cefprozil 250 mg/ 5mL Powder For Oral Suspension Under Fasting Conditions

Healthy

Canada
Ranbaxy Laboratories Limited

Completed

Bioequivalence Study of Cefprozil 250 mg/ 5mL Powder For Oral Suspension Under Fed Conditions

Healthy

Canada
University of Pittsburgh
Organon

Completed

PARIS or PAtch RIng Study: A Trial to Evaluate NuvaRing Versus OrthoEvra (PARIS)

Contraception

United States
Ranbaxy Laboratories Limited

Completed

Bioequivalence Study of Loratadine Orally Disintegrating Tablets 10 mg Under Fed Conditions

Healthy
Ranbaxy Laboratories Limited

Completed

Bioequivalence Study on Loratadine Orally Disintegrating Tablets 10 mg Under Fasting Conditions

Healthy
Ranbaxy Laboratories Limited

Completed

Bioequivalence Study of Clarithromycin 250 mg/5 mL Powder for Oral Suspension Under Fasting Conditions

Healthy

India
Ranbaxy Laboratories Limited

Completed

Bioequivaelnce Study of Clarithromycin 250 mg/5 mL Powder for Oral Suspension Under Fed Conditions

Healthy

India
University Hospital, Basel, Switzerland

Completed

Oral Administration of Peptides; Absorption From Gastrointestinal Tract

Healthy

Switzerland
University of North Carolina, Chapel Hill
Pfizer

Completed

Pharmacist-Administered Injections for Contraception (PAD)

Contraception

United States
Jacobus Pharmaceutical

Terminated

High Dose Oral 4-Aminosalicylic Acid (PASER®) to Control Acute Flares of Mild to Moderate Crohn's Disease

Crohn's Disease

United States, Israel
GlaxoSmithKline

Completed

Evaluation Of SB-751689 Administered At Supratherapeutic Dose Levels In Healthy Adult Subjects.

Osteoporosis

United States
aRigen Pharmaceuticals, Inc.

Unknown

Study to Compare Efficacy of Topical ARYS-01 (Sorivudine) Cream 3%, Oral Valaciclovir and Combination ARYS-01 Cream 3%/Oral Valaciclovir for Treatment of Herpes Zoster (Shingles)

Herpes Zoster | Postherpetic Neuralgia

United States
Boston University

Completed

Mifepristone and Mid-Trimester Termination of Pregnancy

Abortion, Induced | Abortion, Second Trimester

United States
GlaxoSmithKline

Completed

A Two-Part Study to Determine: Best Medication Formulation and Food Effect

Overactive Bladder

United States
Institute of Skin and Product Evaluation, Italy
Aromtech Ltd.

Unknown

Effects of Oral and Topical Sea Buckthorn Oil Treatments on Skin Aging (SBanti-aging)

Skin Aging

Italy
Assistance Publique - Hôpitaux de Paris

Terminated

Amoxicillin Susceptibility of Oral Streptococci After a 3-Day or a 7-Day Amoxicillin Therapy (ODAMOX)

Odontogenic Infection

France
National Institute of Allergy and Infectious Diseases...

Completed

A Treatment Protocol for the Use of Trimetrexate With Leucovorin Rescue for AIDS Patients With Pneumocystis Carinii Pneumonia and Serious Intolerance to Approved Therapies

HIV Infections | Pneumonia, Pneumocystis Carinii

United States
Pfizer

Completed

Chemoprevention of Oral Premalignant Lesions

Precancerous Conditions

United States
National Institute of Allergy and Infectious Diseases...

Unknown

Safety of an Oral HIV Vaccine in HIV Uninfected Volunteers

HIV Infections

United States
Metronome Therapeutics

Unknown

Safety Study of Oral Vinorelbine in Subjects With Non-Hematologic Malignancies

Nonhematologic Malignancies

United States
Winthrop University Hospital

Completed

Optimizing Vitamin D Nutrition in Healthy Adults

Vitamin D Deficiency

United States
Pfizer

Completed

Depo-Provera: Bone Mineral Density and Total Body Calcium in Adolescent DP150CI Users and Non-Hormonal Contraception

Contraception | Bone Density

United States
University of Washington
GlaxoSmithKline

Completed

Oral Androgens in Man-4: (Short Title: Oral T-4)

Contraception

United States
University of Oklahoma

Completed

Pilot Study Combining Temozolomide, Oncovin, Camptosar and Oral Antibiotic in Children and Adolescents With Recurrent Malignancy

Tumors | Lymphomas

United States
Corcept Therapeutics
Eli Lilly and Company

Completed

A Two-Week Study of the Efficacy and Safety of Mifepristone in the Prevention of Olanzapine-Induced Weight Gain

Weight-Gain Prevention

India
Shanghai Changzheng Hospital

Completed

The Effect of the Preoperative Oral Carbohydrate Attenuating Immediate Postoperative Insulin Resistance on PI3K Dependent Signaling Pathway

Colorectal Disease

China
University of Washington
Eunice Kennedy Shriver National Institute of Child Health and Human Development...

Completed

Manipulation of the Intratesticular Hormonal Milieu With Exogenous Testosterone (HOP 5) Testicular Aspiration Addendum (IHOP-5)

Contraception

United States
University of Washington
Eunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaborators

Completed

Oral Androgens in Man-3 (ORAL T-3) Pharmacokinetics of Oral Testosterone

Contraception | Hypogonadism

United States
University of Washington
Eunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaborators

Completed

Male Hormonal Contraceptive Development-ACY-5 (ACY-5)

Contraception

United States
University Hospital Birmingham NHS Foundation Trust

Completed

Anti-Cytokine Therapy for Vasculitis (ACTIVE)

Wegener's Granulomatosis | Microscopic Polyangiitis | Renal Limited Vasculitis

United Kingdom
National Taiwan University Hospital

Available

To Evaluate Oral Phase Swallowing Function Using Submental Ultrasound

Dysphagia
Hacettepe University

Completed

Gingival Wetness and Gingival Crevicular Fluid Volume in Patients With Dry Mouth

Sjogren's Syndrome | Xerostomia

Turkey
Tata Memorial Hospital
Department of Atomic Energy

Completed

Workplace Tobacco Cessation And Oral Cancer Screening Study

Tobacco Cessation | Oral Cancer

India
Dentsply Sirona Implants and Consumables

Terminated

Treatment With Fixture Microthread™ in Patients With Poor Bone Quality and no Teeth in the Upper Jaw, When Using Two-Stage Surgery

Jaw, Edentulous | Poor Bone Quality

United States, Sweden
Bionovo

Terminated

Phase I Study to Evaluate the Safety and Efficacy of MF101 as Well as the Pharmacokinetics of Its Key Active Components

Healthy

United States
National Institute of Allergy and Infectious Diseases...
Bristol-Myers Squibb

Completed

A Study of BMY-27857 in Patients With AIDS or AIDS Related Complex

HIV Infections

United States
Pfizer
National Institute of Allergy and Infectious Diseases (NIAID)

Completed

A Study of Azithromycin Plus Pyrimethamine in the Treatment of a Brain Infection in Patients With AIDS

HIV Infections | Toxoplasmosis, Cerebral

United States
Centers for Disease Control and Prevention
US Department of Veterans Affairs

Completed

TBTC Study 26 PK: Rifapentine Pharmacokinetics in Children During Treatment of Latent TB Infection

Tuberculosis

United States, Canada, Brazil, Spain
National Institute of Allergy and Infectious Diseases...
Bristol-Myers Squibb; Roxane Laboratories

Completed

A Phase I/II Study to Evaluate Single Agent and Combination Therapy With Megestrol Acetate and Dronabinol for the Treatment of HIV-Wasting Syndrome

HIV Infections | Cachexia | HIV Wasting Syndrome

United States

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