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Abnormalities, Multiple clinical trials

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NCT ID: NCT01281644 Completed - Clinical trials for Keratosis Pilaris (KP)

Treatment of Keratosis Pilaris With 810 nm Diode Laser

KP
Start date: March 2011
Phase: N/A
Study type: Interventional

The investigators hope to establish whether or not the diode laser, a longer-wavelength laser, is effective in treating keratosis pilaris, and hopefully opening a door into the discussion and management of this skin condition. The primary outcome of interest is the difference in the overall blind rater severity scores of the treated versus the untreated sites. The secondary outcome of interest is the change in the patient's self-rated severity score of the treated site. To account for potential natural disease progression or regression, the investigators will also compare patient mean changes to the mean changes in severity scores of the untreated site.

NCT ID: NCT00955370 Completed - Clinical trials for Multiple Abnormalities

The Experience of Uncertainty in Parents of Children With an Undiagnosed Medical Condition

Start date: August 4, 2009
Phase: N/A
Study type: Observational

Background: - Rare and undiagnosed conditions are often chronic and disabling, with symptoms affecting different organ systems at various levels of severity. Perhaps the most challenging feature of an undiagnosed medical condition that has lasted 2 or more years is its characteristic uncertainty. In the absence of a diagnosis, health care professionals can provide only limited treatment and prognostic information. - In the case of a child with an undiagnosed condition, the uncertainty that accompanies what is often a chronic, debilitating medical condition and an undefined prognosis may have physical, psychological, social, and spiritual implications for the entire family. Research suggests that parents of a child with an undiagnosed medical condition may be at significantly increased risk of anxiety, depression, poor health, and overall lower quality of life. - It is not well understood how individuals cope with and adapt to chronic uncertainty, and the factors that influence this process. To design future interventions, descriptive studies are needed to reveal predictors that can be manipulated to improve outcomes. Objectives: - To examine whether perceptions of uncertainty, and perceived personal control, are associated with coping and adaptation. - To examine how the length of time elapsed since child was identified as sick and perceptions of uncertainty affect coping and adaptation. - To assess how perceptions of uncertainty, time elapsed since child became sick, optimism, and perceived personal control affect coping and adaptation. Eligibility: - Parents (older than 18 years of age) of children who have an undiagnosed medical condition. - Participants must have a working e-mail address or fixed postal address. Design: - Parents will be recruited from Web-based support networks for parents of undiagnosed children through Web site postings, electronic mailing lists, and printed newsletter postings. - Participants will be asked to complete a questionnaire about their experiences in living with a child who has an undiagnosed but chronic medical condition. The main outcome variable is adaptation to living with one's child's undiagnosed medical condition. - Participants have the option to complete an online or paper version of the questionnaire. The questionnaire should take between 20 and 30 minutes to complete. - No medical treatments are specifically offered as a part of this study.

NCT ID: NCT00944216 Terminated - Keratosis Pilaris Clinical Trials

Efficacy and Safety of Salkera Emollient Foam in the Treatment of Moderate to Severe Keratosis Pilaris, a Prospective Study

Start date: June 2009
Phase: Phase 4
Study type: Interventional

Keratosis pilaris (KP) is a benign skin condition that often is very frustrating for the patients and treating physicians. The investigators are interested to see if the study product is effective in treating moderate to severe KP.

NCT ID: NCT00873678 Completed - Joubert Syndrome Clinical Trials

Assessment of the Prevalence of Genes AHI1, NPHP1 and CEP290 in Joubert Syndrome

JSCORS
Start date: March 2007
Phase: N/A
Study type: Observational

Primary objective: - assessment of the prevalence of AHI1 mutations in Joubert syndrome and cerebello-oculo-renal syndromes (JS/CORS) Secondary objective: - assessment of the prevalence of CEP290 mutations and NPHP1 homozygous deletions in JS/CORS - caracterization of mutational spectrum of AHI1, NPHP1, CEP290 genes in JS/CORS. - evaluation of genotype-phenotype correlation in JS/CORS.

NCT ID: NCT00190411 Completed - Clinical trials for EHLERS-DANLOS SYNDROME, TYPE IV, AUTOSOMAL DOMINANT

Celiprolol in Patients With Ehlers-Danlos Syndrome, Vascular Type

Start date: October 2003
Phase: Phase 4
Study type: Interventional

Ehlers-Danlos syndrome vascular type (EDS-IV) is caused by a genetic defect of collagen type III. Patient die (median 40 yrs) of vascular complications. There is no treatment. We showed that arteries are thin and overloaded in this patients. We test the protective effect of celiprolol on cardiovascular events in a 5 years, randomized, PROBE design

NCT ID: NCT00032877 Completed - Clinical trials for Chromosomal Abnormalities

Genetic Analysis of Fraser Syndrome and Fryns Syndrome

Start date: April 2002
Phase: N/A
Study type: Observational

This study will examine blood or other tissue samples from patients with Fraser syndrome and patients with Fryns syndrome to try to identify the gene responsible for these diseases. Fraser syndrome is characterized by congenital abnormalities including cryptophthalmos (lack of eyelid formation), syndactyly (webbed fingers or toes) and abnormal genitalia. Patients may also have abnormalities of the nose, ears and larynx (voice box), cleft lip or palate, and kidney agenesis. Fryns syndrome is characterized by hernia through the diaphragm, cloudy cornea, coarse facial features, cleft lip or palate, abnormal fingers and toes, heart, kidney and brain malformations and hydrocephalus (accumulation of fluid around the brain). This protocol consists of laboratory study only; it does not involve patient care or patient counseling. Patients with Fraser syndrome or Fryns syndrome are eligible for this study. Parents and healthy siblings of patients will also be included for genetic study, and parents of children with undiagnosed multiple congenital anomalies syndromes will be included for comparison study. Participants will provide a blood sample (about 8 to 10 teaspoons from adults; 1 to 3 teaspoons from children) or sample of skin cells collected by swabbing the inner surface of the cheek. Some patients may undergo a skin biopsy, in which a small skin sample (about 1/8-inch in diameter) is surgically removed. The tissue samples will be used to obtain DNA (genetic material) for laboratory testing. A permanent cell line-a collection of cells grown in the laboratory from the original tissue specimen-will also be established to enable additional testing in the future.

NCT ID: NCT00005102 Recruiting - DiGeorge Syndrome Clinical Trials

Immunologic Evaluation in Patients With DiGeorge Syndrome or Velocardiofacial Syndrome

Start date: January 1995
Phase: N/A
Study type: Observational

OBJECTIVES: I. Determine the pattern of immunologic reconstitution in patients with T-cell compromise due to DiGeorge syndrome or velocardiofacial syndrome. II. Determine any correlation between immunologic function in these patients and chromosome 22 deletion breakpoints. III. Determine presence of sustained immunologic compromise in older patients.