search

Active clinical trials for "Erythema"

Results 71-80 of 112

A Single-Center, Clinical Study to Evaluate the Safety of a New Personal Lubricant in Healthy Female...

ErythemaEdema

To evaluate the safety of a new personal lubricant when used at least four times weekly for two weeks (including at least twice weekly during sexual intercourse for subjects with monogamous male partners), in a population consisting of healthy females.

Completed25 enrollment criteria

The Mysterious on/Off Itch and Erythema During Whole Body Vibration Exercise

Itch; Athlete

Intense itch on the legs sometimes associated with redness can be adverse effects of whole body vibration (WBV) according to own observations and numerous posts in non-professional online-blogs. To the investigators' knowledge, the appearance of itch and/or a rash during WBV exercise has not yet been described. The research objectives are: To determine the effect of WBV on itch rating and its unpleasantness and on skin changes. To determine the effect of WBV on immunoglobulin E (IgE) and serum tryptase

Completed11 enrollment criteria

A Comparison of INSORB Staples With Metal Staples in Total Hip Replacement

ErythemaDrainage2 more

The purpose of this study is to compare the use of INSORB absorbable staples with metal staples on surgical incision healing after total hip replacement. The study evaluates wound healing, complications, and patient satisfaction regarding wound comfort and appearance after surgery.

Completed10 enrollment criteria

Duration of Antibiotic Treatment of Erythema Migrans

Erythema Chronicum Migrans

The purpose of this study is to compare the efficacy of 15-day versus 10-day doxycycline treatment in patients with erythema migrans.

Completed7 enrollment criteria

Influence of Mango Intake of Skin Health in Postmenopausal Women

WrinkleSkin Red

This study aims to investigate the effects on 16 weeks of mango intake on skin health in postmenopausal women. Half of the participants will receive 85g portions of mangoes while the other half receive 250g portions of mangos. Participants will be instructed to consume the specific portion 4 times a week, for a total duration of 16 weeks.

Completed15 enrollment criteria

A Single-Center, Clinical Study to Evaluate the Safety of a Non-Fragranced Personal Lubricant in...

ErythemaEdema

To evaluate the safety of a personal lubricant when used as indicated as a personal lubricant in the vagina and vulvar/perineal areas at least four times weekly for two weeks in a population of healthy females

Completed26 enrollment criteria

A Clinical Study to Evaluate the Safety of a Personal Lubricant in Healthy Female Subjects

ErythemaEdema

To evaluate the safety of a personal lubricant when used at least four times weekly for two weeks (including at least twice weekly during sexual intercourse for subjects with monogamous male partners), in a population consisting of healthy females.

Completed25 enrollment criteria

Photoprotection Efficacy With Sunscreen Formulas Containing the Cyclic Merocyanine Long-UVA Absorber...

PigmentationRedness

To evaluate the photo-protector effect of BC_3 (E212657) formulated in SPF compared to SPF alone on UV Day Light induced pigmentation in healthy volunteers

Unknown status26 enrollment criteria

Clinical Benefit of M89PB in Subjects With Rosacea Associated With Erythema and Sensitive Skin

RosaceaSensitive Skin

The aim of the study is to assess the efficacy of the product M89 probiotic fractions in improving the symptoms of rosacea patients with sensitive skin after 30 days of treatment, in comparison with an area treated with the habitual skin care product. 20 women with sensitive skin (positive reaction to stinging test), suffering from persistent centrofacial erythema of rosacea with no more than 3 papules and pustules apply the product on half a face, twice a day, for 30 days. The subjects use their habitual skin care product on the other side of the face. The product efficacy is supported by significant improvements in the mean basal values of the following instrumental parameters: skin hydration (increase), trans-epidermal water loss (decrease), skin erythema (a* parameter decrease). The efficacy and the tolerability of the product is also showed by a visual clinical assessment of the face skin conditions and by stinging test. Digital images of the face of the subjects were also taken at each control time. Furthermore, the volunteers express their judgement on the efficacy and the pleasantness of the product by means of a self-assessment questionnaire.

Unknown status13 enrollment criteria

A DB Randomized Study of R1 and R2 WaterJel / AloeVera Jell in Prevention of Radiation Dermatitis...

Breast CancerRadiation Dermatitis1 more

The purpose of this study is to evaluate the effects of topical R1 and R2 for prophylaxis of acute radiation dermatitis in patients with breast cancer receiving radiotherapy.

Terminated9 enrollment criteria
1...789...12

Need Help? Contact our team!


We'll reach out to this number within 24 hrs