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Stomatitis clinical trials

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NCT ID: NCT02727062 Active, not recruiting - Oral Mucositis Clinical Trials

Smartphone Pain App for Assessing Oral Mucositis Pain in Patients

Start date: February 13, 2018
Phase:
Study type: Observational

This research is being done to evaluate whether or not the Oral Mucositis (OM) Pain App (a smartphone application) is a feasible and valid tool to assess pain from radiation sores (also referred to as "mucositis") when treating head and neck cancers with radiation. The mobile app will be designed to help people better understand the pain from the radiation sores.

NCT ID: NCT02723604 Completed - Mucositis Clinical Trials

Low-Level Laser Therapy for Prevention of Oral Mucositis

Start date: March 2016
Phase: N/A
Study type: Interventional

The overall purpose of this study is to examine the efficacy of prophylactic low-level laser therapy (LLLT) to reduce the incidence of oral mucositis and adverse events in patients receiving combined modality therapy consisting of chemotherapy and radiation therapy for head and neck cancer.

NCT ID: NCT02696408 Completed - Clinical trials for Hematologic Malignancy

Efficacy of Prophylactic Low Level Laser Therapy (LLLT) Performed by Nurses for Decreasing Severity of Oral Mucositis During Hematopoietic Stem Cell (HSC) Transplantation

STOP MUCITES
Start date: June 27, 2016
Phase: Phase 3
Study type: Interventional

The LLLT has an anti-inflammatory, analgesic effect and accelerates the healing of ulcerated lesions. There are little data in the literature showing its efficacy in prevention of mucositis in cohorts of patients with hematopoietic stem cells transplantation. The main objective of this study is to assess the efficacy of a prophylactic low level laser therapy performed by nurses on the severity of oral mucositis during HSCT.

NCT ID: NCT02686632 Completed - Denture Stomatitis Clinical Trials

The Effectiveness of Palatal Brushing on Denture Stomatitis

Start date: September 2016
Phase: N/A
Study type: Interventional

Denture stomatitis (DS) is an oral biofilm associated inflammatory disease of the palatal mucosa. It is the most prevalent oral disease and the main indicator of poor oral health among denture wearers, affecting one-third of all complete denture wearers. The etiology of DS is multifactorial, with documented role of mechanical trauma, bacteria and fungi. Risk factors may include, poor oral hygiene and nocturnal use of dentures. However, the evidence is ambiguous, inconclusive and recurrence following routine antifungal therapy is common. The proposed study is a phase II clinical trial to evaluate the efficacy of palatal brushing in reducing the colony forming unit (CFU) count and clinical inflammation. The assessment of change in CFU count and clinical inflammation will be carried out at baseline, 3 months and 6 months.

NCT ID: NCT02682992 Completed - Mucositis Clinical Trials

Low-Level Laser Therapy for Prevention of Oral Mucositis

Start date: June 2016
Phase: N/A
Study type: Interventional

The overall purpose of this study is to examine the efficacy of prophylactic low-level laser therapy (LLLT) to reduce the incidence of oral mucositis and adverse events in patients receiving combined modality therapy consisting of chemotherapy and radiation therapy for head and neck cancer.

NCT ID: NCT02662374 Enrolling by invitation - Oral Mucositis Clinical Trials

Oral Hygiene Regimen in Patients on HCT

Start date: September 2015
Phase: Phase 4
Study type: Interventional

Oral mucositis is one of the most common debilitating forms of mucositis that arise from high dose chemotherapy and radiotherapy. It is reported that almost 75% patients undergoing hematopoietic cell transplantation (HCT) develop oral mucositis at different levels of severity. The objective of this prospective study was to assess the efficacy of the addition of supersaturated calcium phosphate oral spray and the addition of an extra soft tooth brush to the basic OH in addition to the currently existing oral hygiene protocol regimen (0.2% Chlorhexidine Gluconate + 3% Sodium Bicarbonate+ Nystatin 100000 U/ml) in reducing the severity of oral mucositis among patients receiving chemotherapy for HCT. 60 patients receiving chemotherapy for HCT were randomly allocated to four groups of 15 patients each The oral mucositis was recorded according to WHO criteria and the progression of the oral mucositis was monitored from the day of admission (day - 1) to the day of discharge (day 28). The absolute neutrophil count, platelet counts and salivary flow rate of all patients was recorded.

NCT ID: NCT02630004 Completed - Oral Mucositis Clinical Trials

Melatonin Oral Gel for Oral Mucositis in Patients With Head and Neck Cancer Undergoing Chemoradiation

MUCOMEL
Start date: November 2015
Phase: Phase 1/Phase 2
Study type: Interventional

The main purpose of this study is to assess the efficacy of melatonin oral gel compared to placebo in the prevention and treatment of oral mucositis in patients with head and neck cancer undergoing concurrent chemoradiation. Other objectives are to assess the Quality of Life (QoL), to evaluate the safety and tolerability and to assess the pharmacokinetic profile of melatonin oral gel administration, in all cases compared to placebo in patients with head and neck cancer and oral mucositis secondary to concurrent chemoradiation.

NCT ID: NCT02608879 Completed - Oral Cancer Clinical Trials

Oral Care Protocol for the Management of Chemotherapy and Radiation Therapy-Induced Oral Mucositis

OMDP
Start date: March 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effects of a novel oral care protocol on the severity and pain of oral mucositis in patients receiving radiation and/or chemotherapy for head and neck cancers. The secondary objectives are to characterize the microbiome associated with oral mucositis, measure salivary proinflammatory cytokines, and evaluate other clinical indicators of the intervention. Participants will be enrolled prior to beginning radiation and/or chemotherapy, and will be randomized to receive either the oral health protocol or standard of care oral hygiene.

NCT ID: NCT02606994 Terminated - Neoplasms Clinical Trials

Effect of Over-the-counter Toothpastes on Chemotherapy-induced Oral Mucositis

TPvsM
Start date: May 29, 2018
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether Oral Defense Toothpaste causes accelerated healing of chemotherapy-induced oral mucositis.

NCT ID: NCT02604329 Completed - Oral Mucositis Clinical Trials

Feasibility Study of a Protocol to Treat Pediatric Oral Mucositis by Low-level Laser Therapy

PEDIALASE
Start date: December 2015
Phase: N/A
Study type: Interventional

Low Level Laser Therapy has been used for a few years in some pediatric hospital centers for chemo- and radiotherapy-induced oral mucositis care. It may promote ulceration's healing, limits mucositis severity and associated pain. As its use is recommended in the treatment of radio induced mucositis in adults, the level of evidence in pediatric studies does not allow a precise treatment protocol. The investigators present here the protocol of a feasibility study in the haemato-oncology department of the Children University Hospital of Toulouse, with the view to a future efficacy study.