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Mucositis clinical trials

View clinical trials related to Mucositis.

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NCT ID: NCT01876407 Recruiting - Oral Mucositis Clinical Trials

Effectiveness of Low Energy Laser Treatment in Oral Mucositis Induced by Chemotherapy and Radiotherapy in Head and Neck Cancer

Start date: January 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of using to low intensity laser as an intervention against preventive and therapeutic oral mucositis induced by radiotherapy and chemotherapy.

NCT ID: NCT01806272 Recruiting - Clinical trials for Nasopharyngeal Cancers

Recombinant Human Granulocyte Macrophage Colony Stimulating Factor(rhGM-CSF) Treating Oral Mucositis

Start date: March 2013
Phase: Phase 2
Study type: Interventional

This is a open,randomized phase II trial comparing effectiveness and safety of local use of rhGM-CSF and Compound Vitamin B12 to Compound Vitamin B12 solution alone treating oral mucositis in primary nasopharyngeal cancer. The main end point is the incidence of grade II and less oral mucositis at the end of treatment.The hypothesis of the study is that the local use of rhGM-CSF and Compound Vitamin B12 can decrease the incidence of grade III and more oral mucositis at the end of treatment compared to local use of Compound Vitamin B12 alone.

NCT ID: NCT01762514 Recruiting - Mucositis Clinical Trials

A Phase II Clinical Trial on Comparison of Effectiveness and Safeness of Different Amifostine Regimens

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

RATIONALE - Radiotherapy is the primary therapeutic strategy for nasopharyngeal carcinoma. - Radiotherapy may cause adverse effect such as xerostomia and mucositis. - Amifostine has the ability of protecting the normal tissue but also has some side effects. PURPOSE - This phase II trial is to study the protecting effect and safety of different Amifostine regimens in patients with nasopharyngeal carcinoma.

NCT ID: NCT01707641 Recruiting - Mucositis Clinical Trials

Effect of Lactobacillus Brevis CD2 in Prevention of Radio-chemotherapy Induced Oral Mucositis in Head and Neck Cancer

Start date: November 2012
Phase: Phase 4
Study type: Interventional

Oral mucositis is a debilitating side effect for oncology patients and there is a clear need for new therapeutic options. The lozenges containing Lactobacillus brevis CD2 proved a potential new alternative for the prevention of grade III and IV mucositis. The main endpoint of this study is to verify if these lozenges taken 6 times a day may reduce the incidence of grade III and IV mucositis as well as increase the percentage of patients who will complete the radio-chemotherapy treatment.

NCT ID: NCT01432873 Recruiting - Clinical trials for Hematopoietic Stem Cell Transplantation

Oral Selenium Therapy for the Prevention of Mucositis

Start date: June 2011
Phase: Phase 1/Phase 2
Study type: Interventional

Selenium as an antioxidant and anti-inflammatory agent could be effective in prevention of mucositis induced by chemotherapy and radiotherapy. Other agents such as vitamin E, Zinc sulfate, amifostine, beta carotene and benzidamine are indicated for prevention of mucositis and positive effects are seen. Our purpose in this double blinded randomized study is to evaluate the selenium effect on mucositis prevention in patient with acute myeloid leukemia (AML) & acute lymphoblastic leukemia (ALL) whose received Busulfan and/or Cyclophosphamide before Hematopoietic stem cell transplantation (HSCT).

NCT ID: NCT01420562 Recruiting - Clinical trials for Allogeneic Hematopoietic Stem Cell Transplantation (HSCT)

Pharmacokinetics of Posaconazole in Allogeneic Transplant Patients With Mucositis

Start date: September 2011
Phase: N/A
Study type: Observational

The goal of this study is to calculate pharmacokinetic parameters and to evaluate the trough levels of posaconazole reached in patients with different stages of mucositis, due to chemotherapy and total body irradiation.

NCT ID: NCT01318889 Recruiting - Clinical trials for Oral Mucositis (Ulcerative) Due to Radiation

Dexpanthenol Mouthwash to Treat Oral Mucositis

Start date: September 2010
Phase: Phase 2
Study type: Interventional

Oral mucositis can be a significant problem for cancer patients. It is typically associated with pain and increased risk of infection and can lead to impaired nutritional status and inadequate hydration.it can be seen in the patient population receiving high-dose head and neck radiation therapy (85%-100%). Topical dexpanthenol acts like a moisturizer, improving stratum corneum hydration, reducing transepidermal water loss and maintaining skin softness and elasticity. The stimulation of epithelization, granulation and mitigation of itching were the most prominent effects of formulations containing dexpanthenol. The investigators suppose that dexpanthenol mouth wash may improve oral mucositis.

NCT ID: NCT01007617 Recruiting - Oral Mucositis Clinical Trials

Low-energy Laser Therapy for Prevention of Oral Mucositis in Children

Start date: June 2009
Phase: Phase 2/Phase 3
Study type: Interventional

Oral mucositis represents a major complication of cytotoxic chemotherapy among cancer in children. Low-power laser therapy (LPLT) has been used to reduce the incidence of oral mucositis in patients who are receiving high-dose chemotherapy. The aim of this study is to compare two preventives energies delivered of LPLT to oral mucosa in decreasing the severity of mucositis in children.

NCT ID: NCT00901732 Recruiting - Oral Mucositis Clinical Trials

Caphosol for the Reduction of Mucositis in Patients Receiving Radiation Therapy for Head and Neck Cancer

Start date: May 2009
Phase: Phase 1/Phase 2
Study type: Interventional

Patients who have been diagnosed with a head and/or neck cancer commonly develop oral mucositis (OM). The purpose of this study is to estimate the effect of Caphosol on OM and to evaluate if Caphosol had any effect on clinical outcomes which include quality of life, oral intake, swallowing function and pain.

NCT ID: NCT00563498 Recruiting - Mucositis Clinical Trials

Effects on Glutamine on the Outcome of Allogeneic Bone Marrow Transplant Recipients

Start date: July 2004
Phase: N/A
Study type: Interventional

The primary purpose of this project is to investigate if addition of glutamine, an amino acid, to standard parenteral nutrition, may improve the clinical outcome of the bone marrrow transplantation reducing the occurrence of veno-occlusive disease and severity of mucositis.