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Skin Burning Sensation Medical Research Studies

Up-to-date List of Skin Burning Sensation Medical Research Studies

What Research is Being Done?

A clinical study involves research using human volunteers (also called participants) that is intended to add to medical knowledge. There are two main types of clinical studies: clinical trials (also called interventional studies) and observational studies. Following list includes both interventional and observational studies.

Latest Skin Burning Sensation Medical Research Studies

Rank Status Study
1 Unknown  Non-inferiority Clinical Trial of Dexchlorpheniramine (Cream Versus Gel) in the Relief of Sunburn Related Symptoms
Condition: Sunburn
Interventions: Drug: Dexchlorpheniramine 1% gel;   Drug: Dexchlorpheniramine 1% cream
Outcome Measures: Pruritus intensity evaluated with a 10-point Visual Analogic Scale (VAS);   Composite clinical evaluation of erythema, pruritus and burning sensation performed by the investigator using a 4-point scale for each one of the variables (absent, mild, moderate, intense).
2 Unknown  Non-inferiority Clinical Trial of Dexchlorpheniramine (Cream Versus Lotion) in the Relief of Sunburn Related Symptoms
Condition: Sunburn
Interventions: Drug: Dexchlorpheniramine 1% lotion;   Drug: Dexchlorpheniramine 1% cream
Outcome Measures: Pruritus intensity evaluated with a 10-point Visual Analogic Scale (VAS);   Composite clinical evaluation of erythema, pruritus and burning sensation performed by the investigator using a 4-point scale for each one of the variables (absent, mild, moderate, intense).
3 Unknown  Sensory Mapping Following Video-assisted Thoracic Surgery
Conditions: Paresthesia;   Dysesthesia;   Pain
Intervention:
Outcome Measures: Area (cm2);   Pain
4 Unknown  Comparison Between Elliptical Domed Mesh Technique and Lichtenstein Technique in Inguinal Hernia
Condition: Inguinal Hernia
Intervention: Procedure: Elliptical domed mesh technique
Outcome Measures: pain one month after surgery;   pain three months after surgery;   pain six months after surgery;   dysesthesia one month after surgery;   dysesthesia three months after surgery;   dysesthesia six months after surgery
5 Recruiting Prevention of Oxaliplatin-induced Neuropathic Pain by a Specific Diet
Conditions: Neuropathy;   Digestive Cancer System
Intervention: Behavioral: Polyamines depleted diet, associating Polydol® cans and predefined menus low in polyamines
Outcome Measures: Cold pain thresholds;   Heat pain thresholds;   DN4 (Douleur Neuropathique en 4 Questions) scores;   HADS (Hospital Anxiety and Depression Scale) score;   Adverse drug reactions (CTCAE (Common Terminology Criteria for Adverse Events));   Cancer response;   Oxaliplatin dose intensity;   Erythrocyte polyamine levels;   NPSI ( Neuropathic Pain Symptom Inventory)scores;   QLQ-C30 (Quality of Life questionnaire C30)scores
6 Recruiting Investigation of Efficacy of incobotulinumtoxinA (Xeomin) in Relieving Symptoms of Restless Leg Syndrome.
Condition: Restless Leg Syndrome
Interventions: Drug: incobotulinumtoxinA;   Drug: Placebo
Outcome Measures: Restless Leg Syndrome Rating Scale;   Epworth Sleep Scale
7 Recruiting Preemptive Treatment With XONRID to Reduce Radiation Induced Dermatitis in Head and Neck Cancer Patients
Condition: Head and Neck Cancer
Intervention: Device: XONRID
Outcome Measures: Worst skin toxicity;   MeanPatient Reported Outcome (PRO);   Median time to G2 radiation dermatitis development;   Compliance;   Grade of late toxicity
8 Recruiting Nerve Stimulator Versus Ultrasound-guided Infraclavicular Block
Condition: Pain
Interventions: Procedure: NS-guided infraclavicular block;   Procedure: US-guided infraclavicular block
Outcome Measures: Duration of postoperative analgesia;   block performance time;   number of needle redirections;   patient discomfort;   paresthesia;   onset time;   motor block of hand;   postoperative dysesthesia;   supplemental analgesia;   Pain score;   Patient satisfaction
9 Recruiting Peripheral Sensory Input in Central Post Stroke Pain (CPSP)
Condition: Central Post Stroke Pain
Intervention: Drug: Ultrasound-guided peripheral nerve block with 2% lidocaine
Outcome Measures: Reduction in spontaneous pain intensity in the painful extremity 20-30 minutes after a peripheral nerve block.;   Change in the intensity of cold sensation;   Change in the intensity of warm sensation;   Change in the intensity of pinprick sensation;   Change in the intensity of brush sensation;   Reported pain/dysesthesia descriptors on NPSI questionnaire;   Correlation between change in spontaneous pain vs. change in intensity of evoked hypersensitivity.
10 Recruiting Efficacy of Pulsed Light Therapy for Meibomian Gland Dysfunction and Dry Eye Syndrome
Conditions: Meibomian Gland Dysfunction;   Dry Eye Syndrome
Interventions: Device: Cutera Xeo Platform-Limelight;   Device: Sciton BroadBand Light
Outcome Measure: Anatomical improvement of the meibomian glands and their secretions.
11 Recruiting Temporal Artery Biopsy vs ULtrasound in Diagnosis of GCA (TABUL)
Condition: Giant Cell Arteritis
Interventions: Procedure: Ultrasound of temporal and axillary arteries;   Procedure: Temporal artery biopsy
Outcome Measures: To evaluate the diagnostic accuracy (sensitivity and specificity) of ultrasound as an alternative to temporal artery biopsy for the diagnosis of GCA in patients referred for biopsy with suspected GCA.;   To evaluate the cost-effectiveness (incremental cost per QALY) of ultrasound instead of biopsy in the diagnosis of GCA.;   To evaluate inter-observer agreement in the assessment of ultrasound and temporal artery biopsy;   To elicit expert views on the appropriateness of performing a biopsy following ultrasound using clinical vignettes;   To evaluate the diagnostic accuracy (sensitivity and specificity) of the sequential diagnostic strategy as an alternative to temporal artery biopsy alone in the diagnosis of GCA;   To evaluate the cost-effectiveness (incremental cost per QALY) of the diagnostic strategy of combined ultrasound and biopsy instead of biopsy alone in the diagnosis of GCA.;   Specific adverse events measured at each assessment; daily and cumulative steroid dose; steroid side effects; and pain or dysaesthesia at the biopsy site.;   Evolution of an alternative diagnosis;   Negative predictive value of ultrasound in preventing the need for temporal artery biopsies.;   Cost analysis of performing a screening ultrasound examination plus biopsy as part of the diagnostic workup of all patients with suspected GCA; or of performing a screening ultrasound examination instead of biopsy; or of performing a screening ultrasound;   Cost analysis of performing a screening ultrasound examination instead of biopsy in cases with a very low probability of GCA as part of the diagnostic workup of all patients with suspected GCA.;   Prediction of potential harm done to patients by over diagnosis or under diagnosis of GCA as a result of ultrasound use, either alone or in combination with biopsy;   Value of axillary artery ultrasound scanning in contributing to the diagnosis of GCA.;   Analysis of proportion of patients with a biopsy positive halo, stenosis, or occlusion assessed by high resolution ultrasound;   Presence of characteristic features of GCA on temporal artery biopsy in relation to clinical and ultrasound findings
12 Recruiting Topical Green Tea Ointment in Treatment of Superficial Skin Cancer
Condition: Carcinoma, Basal Cell
Interventions: Drug: Sinecatechins 10%;   Drug: Placebo
Outcome Measures: Percentage of patients with complete histological clearance;   Number of applications actually done by the patient divided by the total prescribed number of applications.;   Number of local skin reactions, adverse events and serious adverse events
13 Recruiting Effect of Gluten Free Diet in Patients With Burning Mouth Syndrome
Condition: Burning Mouth Syndrome
Interventions: Dietary Supplement: Gluten Free Diet;   Dietary Supplement: Normal Diet
Outcome Measures: oral pain;   Quality of Life
14 Recruiting Acupuncture in Herpes Zoster Neuralgia (ACUZoster)
Conditions: Herpes Zoster;   Postherpetic Neuralgia;   Pain
Interventions: Device: Sham-laser acupuncture;   Drug: gabapentine;   Procedure: Acupuncture
Outcome Measures: Alteration of pain intensity after treatment;   Quantitative sensory testing
15 Unknown  Effect of Fluticasone Proprionate 0.05% on Narrow Band UV-B in Active Vitiligo
Conditions: Patients With Active Non-segmental Vitiligo.;   Evaluation of the Efficacy of UVB and Fluticason Proprionate 0.05%;   Cream Compared to NB-UVB Alone in Patients With Non-segmental Vitiligo
Intervention: Drug: Fluticasone proprionate 0.05% cream
Outcome Measures: Repigmentation of the vitiligo lesions;   Patients satisfaction
16 Recruiting A Trial of Gemcitabine, Infusional 5-Fluorouracil and Cisplatin for Advanced Pancreatic and Biliary Cancers
Conditions: Pancreatic Cancer;   Biliary Cancer
Intervention: Drug: Gemcitabine, 5-FU and Cisplatin
Outcome Measures: Response rate;   Survival
17 Unknown  Trial on the Efficacy of Tegaderm Chlorhexidine Gluconate (CHG) in Reducing Catheter Related Bloodstream Infections
Conditions: Catheterization;   Infection
Intervention: Device: Transparent adhesive dressing with an integrated gel pad containing 2% w/w chlorhexidine gluconate (CHG) (TegaDerm CHG)
Outcome Measures: Incidence of catheter-related bloodstream infection;   Incidence of adverse events
18 Unknown  Burning Mouth Disorder (BMD) - A Neuropathic Pain Disorder
Conditions: Burning Mouth Syndrome;   Taste Disorder;   Orofacial Pain
Intervention:
Outcome Measure: Neurosensory differences between Burning Mouth Disorder patients and controls.
19 Recruiting TRPV Expression in Subjects With Sensitive Skin
Condition: Sensitive Skin
Interventions: Procedure: Skin biopsy;   Procedure: Oral mucosa specimen
Outcome Measures: Expression of TRPV1;   TRPV1 and Sensitive Skin;   TRPV1 and skin phototype;   TRPV1 and barrier function
20 Recruiting The Effects of Therapeutic Resources on Structure and Function of Normal and Burned Skin
Conditions: Burn;   Skin Graft
Interventions: Device: ultrasound;   Device: paraffin;   Device: endermotherapy
Outcome Measures: Elasticity of skin and scar;   Erythema of skin and scar;   Fiber direction of skin and scar

These studies may lead to new treatments and are adding insight into Skin Burning Sensation etiology and treatment.

A major focus of Skin Burning Sensation research is the development of new drugs and other treatment options. Studies seek to identify new drugs to treat various related disorders and to find safer, more effective doses for medications already being used. Other research is aimed at identifying receptors or drug targets.


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