Clinical Trials Logo

Facies clinical trials

View clinical trials related to Facies.

Filter by:

NCT ID: NCT02139618 Completed - Facial Photodamage Clinical Trials

Efficacy of Methyl Aminolevulinate + Daylight in Patients With Facial Photodamage

Start date: April 2014
Phase: Phase 2
Study type: Interventional

Treatment of actinic damage has included multiple procedures but to date there is limited scientific evidence to support the preferential use of one of these therapies according to their efficacy, safety and pain tolerance by patients. This study aims to assess the efficacy of methyl aminolevulinate + daylight vs placebo + daylight to treat facial photodamage

NCT ID: NCT02110108 Completed - Clinical trials for Facial Solar Lentigines

Study for the RevLite Laser System for Facial Solar Lentigines

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

The purpose of this study is to evaluate the effects of the Revlite Laser System for treatment of facial solar lentigines

NCT ID: NCT02107157 Completed - Facial Rejuvenation Clinical Trials

Clinical and Histological Evaluation of the Picosure 755nm Laser With Cap Array for Facial Rejuvenation

Start date: July 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to assess treatment of facial rejuvenation using the standard hand piece and a Lens Array for the 755nm Alexandrite laser.

NCT ID: NCT02024724 Completed - Clinical trials for Atypical Facial Pain

Ultrasound Guided Trigeminal Nerve Block for Typical or Atypical Facial Pain

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

Trigeminal neuralgia is a craniofacial pain syndrome that is typically characterized by unilateral severe, recurrent, electrical pain in one or more distributions of the trigeminal nerve. Current treatment strategies include oral medications as first line therapy with surgical interventions reserved for those patients who are refractory to medications or unable to tolerate medication side effects. Despite these current treatment options, many patients continue to have symptoms. Ultrasound-guided trigeminal nerve block allows for fine adjustment of the needle tip and direct observation of the medicine. Local anesthetic and steroids have been successfully used for diagnostic and or therapeutic nerve pain with great success. Steroids can be short or long acting in duration with varying side effects. If there exists a difference in duration of action, using the longer acting drug will provide a greater period of symptom relief for the patient and may allow the patient to undergo fewer interventional procedures.

NCT ID: NCT02009462 Completed - Clinical trials for HIV-facial Lipoatrophy

Artefill for the Treatment of HIV-associated Facial Lipoatrophy

Start date: December 2013
Phase: Phase 1
Study type: Interventional

Artefill is an injectable facial filler device that is currently approved by the FDA for the correction of nasolabial folds. This study seeks to examine the use of Artefill in the treatment of HIV associated facial lipoatrophy. Facial lipoatrophy (facial fat loss) related to HIV is a stigmatizing condition characterized by loss of facial fat, most notably in the cheeks and temples.

NCT ID: NCT02002572 Completed - Clinical trials for Mimic Facial Muscles

Quantification, Analysis and Simulation of Facial Mimics Movements

SIMOVI-IRM
Start date: August 8, 2011
Phase: N/A
Study type: Interventional

The SIMOVI project is a collaboration between our Department of Maxillofacial Surgery (CHU Amiens) and the Biomechanical bioengineer Research Department and Roberval Labs (Technological University of Compiègne). The question raised is the extent to which a facial mimic can be evaluated objectively. In today's clinical practice, the investigators use grading systems based on muscular scale or testing, in order to evaluate a facial muscular disorder. This assessment remains subjective because the investigators are deducing from surfacing cutaneous deformations the movement quality of the solicited muscle. This qualitative approach is therefore an approximate approach and deserves to be better thought to plan a surgical treatment which involves mimic facial muscle (as rehabilitation of facial palsy, cleft palate for example), to monitor the results, and to follow the recovery and progress in physiotherapy care. The aim of this study is to correlate external soft tissue movement (essentially cutaneous) during facial mimic with internal movement (essentially facial mimic muscle) using qualitative and QUANTITATIVE indicators, and to perform a biomechanical model of selected mimic face's movement using the precedent data.

NCT ID: NCT01853423 Completed - Facial Angiofibroma Clinical Trials

Tuberous Sclerosis Complex: Facial Angiofibroma Skin Cream

Start date: October 2013
Phase: Phase 1
Study type: Interventional

The objective of this study is to evaluate the safety and efficacy of a 0.1% formulation of rapamune cream in children with Tuberous Sclerosis Complex (TSC), ages 3 years and older, who have facial angiofibromas that would benefit from treatment.

NCT ID: NCT01746355 Completed - Clinical trials for Atypical Facial Pain or Atypical Odontalgia

Assessment and Treatment Patients With Atypical Facial Pain Trough Repetitive Transcranial Magnetic Stimulation

EMTr-AFP
Start date: March 2011
Phase: N/A
Study type: Interventional

Atypical Facial Pain is a chronic condition and presents controversies during diagnostic and treatment, between specialist not have consensus about the pathophysiology. It is possible consider this entitie a potential neuropathic cause without pathological signs. It knows the repetitive transcranial magnetic presents good results in the treatment of chronic pain coditions. The aim this study is evaluated the thresholds and excitability cortical in patients with AFP and verify the patterns of improvement in pain for patients undergoing rTMS compared to controls, as well as the therapeutic response to neuromodulation procedures. This enroll 20 patients with DAF and 20 controls treated with rTMS (5 sessions) and evaluated through questionnaires (EDOF clinical record, McGill Pain Questionnaire, Visual Analogue Scale, Inventory of symptoms of neuropathic pain, neuropathic pain DN4 questionnaire, SF -36, brief pain inventory). At the end of the data will be statistically analyzed and expressed as mean and standard deviation, and analyzed by Student's t test, analysis of variance (ANOVA), Tukey-Kramer and Pearson correlation. The level of significance is 5%. The results will be published in journals indexed in the area both nationally and internationally and presented at conferences and scientific meetings.

NCT ID: NCT01740440 Completed - Facial Aging Clinical Trials

Effect of a Transcutaneous Electrical Nerve Stimulation (TENS) Device on Overall Facial Appearance

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

The primary objective of this clinical study is to evaluate the clinical performance of the BMR Face device (manufactured by Bio-Medical Research) for the overall facial appearance using a grading scale. Secondary objectives are to evaluate safety and further evaluate the subject's and investigator's satisfaction (both a live and blinded assessor) with the BMR Face treatment.

NCT ID: NCT01658644 Completed - Clinical trials for Effects of Photographic Aids (Photos of Faces) on Overall Patient Satisfaction

Put a Face to a Name (Part A): The Effects of Photographic Aids on Patient Satisfaction, Clinician Communication, and Quality of Care

Face2Name
Start date: August 2012
Phase: N/A
Study type: Interventional

Communication is critical within healthcare, and is the root cause of most errors. With increased adoption and use of new information technologies and mediated communication systems, such as Electronic Health Records (EHR), that support visual content, hospitals can begin to look at the potential of photographic aids to improve patient satisfaction, clinician communication, and ultimately quality of care. Having pictures of clinicians and patients may improve communication by improving knowledge of who is part of the care team and may reduce electronic ordering or documentation on the wrong patient. Despite the importance of communication between clinicians and the many advances within information and communication technologies, there is a lack of literature documenting systems that are effective at improving communication. Our research study will provide an overview on the communication models and technologies used in Canadian hospitals and add insights to the impacts of these technological adoption. Research Question: How does the use of photographic influence patients' hospital experience? Specifically, do photographic aids (photographs of clinicians' faces) influence: 1. Patient's ability to identify their clinical care team members 2. Patient's ability to identify their care team members and know their individual roles 3. Patient's satisfaction with their hospital experience