Search clinical trials for: itch

Total 356 results

Trevi Therapeutics

Completed

Open Label Extension Study of Nalbuphine HCl ER in Hemodialysis Patients With Uremic Pruritus

Pruritus | Uremic Pruritus

United States
Mansoura University

Unknown

Effect of Intravenous Magnesium on Post-spinal Fentanyl Induced Pruritus Incidence

Magnesium Infusion in Post-spinal Opioid Pruritis

Egypt
Cairo University

Completed

Paraffin Bath Therapy for Chronic Hand Eczema

Eczema

Saudi Arabia
Cara Therapeutics, Inc.

Completed

Study to Evaluate IV CR845 in Hemodialysis Patients With Moderate-to-Severe Pruritus

Uremic Pruritus

United States
Aalborg University

Completed

A Relation of Morphine-induced Itch and Pain Processing

Morphine | Itch

Denmark
Aalborg University

Completed

A Mechanistic Evaluation of the Interactions Between Thermoceptive and Pruriceptive Sensory Processing

Itch | Histamine | Cowhage | Thermal Stimulation | Serotonine

Denmark
Indonesia University

Completed

Scalp Pruritus Measurement Using Visual Analog Scale and 5-d Itch Scale in Children With Pediculosis Capitis

Pruritus | Pediculus Capitis

Indonesia
Pfizer

Completed

Open-Label Extension Study Of Tofacitinib In Psoriatic Arthritis (OPAL BALANCE)

Arthritis, Psoriatic

Belgium, United States, Canada, Spain, Australia, Taiwan, Czechia, Hungary, Germany, Mexico, Poland, Russian Federation, Slovakia, United Kingdom, Brazil, Bulgaria
Johns Hopkins University

Completed

The Role of Skin Care Regimen in Skin Health

Itching | Xerosis

United States
Amgen

Completed

A Study of the Efficacy and Safety of Apremilast (CC-10004) in Subjects With Moderate to Severe Plaque Psoriasis of the Scalp (STYLE)

Psoriasis

United States, Canada
Jean Yuh Tang
Vyne Therapeutics Inc.; Epidermolysis Bullosa Research Partnership

Completed

Neurokinin-1 Receptor Antagonist for the Treatment of Itch in EB Patients

Pruritus | Epidermolysis Bullosa

United States
Royal North Shore Hospital

Unknown

Laser Therapy for Vulvovaginal Symptoms in Breast Cancer Patients (LAAVA2)

Vulvovaginal Atrophy | Genitourinary Symptoms and Ill-Defined Conditions

Australia
Actavis Inc.
Watson Laboratories, Inc.

Completed

A Multi-center, Double-blind, Randomized Study, Comparing Clindamycin Phosphate Vaginal Cream 2% (Watson Laboratories, Inc.) to Clindesse® (Ther-Rx™, Clindamyin Phosphate Vaginal Cream 2%) and Both Active Treatments to a Placebo Control in the Treatment of Bacterial Vaginosis in Non-pregnant Women

BACTERIAL VAGINOSIS | Signs and Symptoms to be Evaluated and Recorded Include | Vaginal Discharge Color, Odor, and Consistency | Vulvovaginal Itching and Irritation (Subjective) Absent, Mild, Moderate, or Severe | Vulvovaginal Inflammation (Objective) Absent, Mild, Moderate, or Severe

United States, Dominican Republic, Puerto Rico
Novartis Pharmaceuticals

Completed

Study of Efficacy and Safety of Secukinumab in Subjects With Moderate to Severe Chronic Plaque-type Psoriasis

Plaque Psoriasis

China, Thailand, Philippines, Turkey, Hungary, Malaysia
Aalborg University

Unknown

Characterization of Bovine Adrenal Medulla (BAM8-22) as a New Surrogate Model of Non-histaminergic Itch

Itch

Denmark
GlaxoSmithKline
Quintiles, Inc.

Completed

A PH I Pilot Imaging Study to Evaluate Molecular Imaging Methods in HVs and pSS Pts

Autoimmune Diseases

United Kingdom
Novartis Pharmaceuticals

Completed

A Study to Evaluate Clear Skin Effect on Quality of Life in Patients With Plaque Psoriasis. (PROSE)

Plaque Psoriasis

Germany, United Kingdom, Belgium, Czechia, Estonia, Italy, France, Israel, Spain, Bulgaria, Lithuania, Portugal, Poland, Romania, Latvia, Greece, Slovakia
Leiden University Medical Center

Completed

Immunisation, Treatment and Controlled Human Hookworm Infection (ITCHHI)

Necator Americanus Infection

Netherlands
Sheffield Teaching Hospitals NHS Foundation Trust
Obstetric Anaesthetist's Association

Completed

Acupuncture for Prevention of Itch in Caesarean Section

Pruritus

United Kingdom
Glenmark Pharmaceuticals Ltd. India

Completed

To Study Generic Tacrolimus Ointment, 0.1% in the Treatment of Moderate to Severe Atopic Dermatitis (Inflammation of Skin: Itchy, Red, Swollen, and Cracked Skin)

Atopic Dermatitis

United States
University Hospital, Basel, Switzerland

Completed

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

Itch; Athlete

Switzerland
Allergan

Completed

Safety and Efficacy of Lastacaft® for the Prevention of Itching Associated With Allergic Conjunctivitis in Korea

Conjunctivitis, Allergic

Korea, Republic of
Novartis Pharmaceuticals

Completed

Secukinumab Dosage Optimisation in Partial Responders With Moderate to Severe Plaque-type Psoriasis (GAIN)

Moderate to Severe Plaque-type Psoriasis

Germany
Kaohsiung Medical University

Unknown

Botulinum Toxins Intralesional Injection for Scar Pain

Hypertrophic Scar | Scar Keloid

Taiwan
Washington University School of Medicine

Withdrawn

Relieving Chronic Itch: Oral Medication (CIPS)

Pruritis
University Hospital, Basel, Switzerland

Completed

The Color of Itch; Itch Modification by Color Viewing

Pruritus | Itch

Switzerland
Diamant Thaci

Withdrawn

Analysis of the Pathogenesis of Itch in Response to Apremilast Therapy in Psoriasis Patients (Itch)

Moderate to Severe Plaque Psoriasis

Germany
Novartis Pharmaceuticals

Completed

Study to Evaluate Psoriasis Severity and Its Psychosocial Impact Using the Simplified Psoriasis Index (SPI), as Well as Long-term Safety, Tolerability and Efficacy of Secukinumab Administered Subcutaneously in Patients With Moderate to Severe Psoriasis (IPSI-PSO)

Psoriasis

France
Pfizer

Completed

A Study Evaluating The Efficacy And Safety Of CP-690,550 In Asian Subjects With Moderate To Severe Plaque Psoriasis

Psoriasis

Korea, Republic of, Taiwan, China
Dynavax Technologies Corporation

Terminated

Efficacy and Safety Study of TOLAMBA™ in Ragweed-Allergic Adults

Rhinitis, Allergic, Seasonal

United States
Xiangya Hospital of Central South University

Completed

Treatment of Chronic Itch in Patients Under Arsenic Exposure With Sublingual Naloxone

Chronic Pruritus

China
University Hospital, Basel, Switzerland

Completed

Survey on Itch in Outpatients of a University Clinic

Itch

Switzerland
Mirum Pharmaceuticals, Inc.
Childhood Liver Disease Research and Education Network

Completed

Evaluation of LUM001 in the Reduction of Pruritus in Alagille Syndrome (ITCH)

Alagille Syndrome

United States, Canada
Mirum Pharmaceuticals, Inc.

Completed

Validation of the Itch Reported Outcome (ItchRO) Diaries in Pediatric Cholestatic Liver Disease

Alagille Syndrome | Progressive Familial Intrahepatic Cholestasis

United States, Canada
National Institute of Allergy and Infectious Diseases...

Completed

Comparing the Efficacy, Safety, and Tolerability of Combination Antivirals (Amantadine, Ribavirin, Oseltamivir) Versus Oseltamivir for the Treatment of Influenza in Adults at Risk for Complications (IRC003)

Influenza

United States, Australia, Argentina, Mexico, Thailand
Pfizer

Completed

A Phase 3, Multi Site, Randomized, Double Blind, Placebo Controlled Study Of The Efficacy And Safety Comparing CP- 690,550 And Etanercept In Subjects With Moderate To Severe Chronic Plaque Psoriasis

Psoriasis

Belgium, Spain, Germany, France, Hungary, Russian Federation, Singapore, Argentina, Austria, Bosnia and Herzegovina, Bulgaria, Chile, Colombia, Croatia, Czechia, Denmark, Hong Kong, Israel, Korea, Republic of, Netherlands, Poland, Slovaki... and more
Pfizer

Completed

A Study To Evaluate The Effects And Safety Of Treatment, Treatment Withdrawal, Followed By Re-Treatment With CP-690,550 In Subjects With Moderate To Severe Chronic Plaque Psoriasis

Psoriasis

United States, Denmark, Slovakia, Canada, Australia, Argentina, Bulgaria, Netherlands, United Kingdom, Brazil, Finland, Greece
Virginia Commonwealth University

Terminated

Study of Using Long Acting Antihistamine to Treat Opioid Induced Itching

Pruritus

United States
Laboratorios Sophia S.A de C.V.

Withdrawn

Efficacy and Safety of PRO-118 Ophthalmic Solution in Allergic Conjunctivitis (PRO-118)

Conjunctivitis, Allergic | Seasonal Allergic Conjunctivitis | Ocular Itching | Ocular Allergy | Perennial Allergic Conjunctivitis

Mexico
Novartis Pharmaceuticals

Completed

Judging the Efficacy of Secukinumab in Patients With Psoriasis Using AutoiNjector: a Clinical Trial Evaluating Treatment Results (JUNCTURE) (JUNCTURE)

Plaque-type Psoriasis

Germany, United States, France, Estonia, Canada
Johnson & Johnson Consumer Products Company Division...

Completed

Clinical Trial to Assess the Effects of Topical Lotions on Changes in the Skin Microbiome and Associations With Itch

Microbiota

United States
Novartis Pharmaceuticals

Completed

OPTIMA: Efficacy of Optimized Re-treatment and Step-up Therapy With Omalizumab in Chronic Spontaneous Urticaria (CSU) Patients (OPTIMA)

Chronic Spontaneous Urticaria

Argentina, Dominican Republic, Canada, Brazil, Guatemala, Chile, Mexico, Panama
Wake Forest University
Stiefel, a GSK Company

Completed

Comparative Study of the Efficacy of SARNA Sensitive Lotion for Treatment of Uremic Itch in Adult Hemodialysis Patients

Pruritis

United States
Wake Forest University
Medicis Pharmaceutical Corporation

Completed

Efficacy of Fluocinonide Cream 0.1% (Vanos(R)) in Reducing Itch in Subjects With Atopic Dermatitis

Atopic Dermatitis

United States
Emory University

Completed

Study of Kids Itch Severity (SKIS) (SKIS)

Chronic Pruritus

United States
Alta Bates Summit Medical Center

Terminated

GSM (Genitourinary Syndrome Of Menopause) Management In Breast Cancer Survivors (GSM)

Urinary Tract Infections | Breast Cancer Female | Dyspareunia | Dysuria | Genitourinary Abnormality | Vaginal Abnormality

United States
Patara Pharma

Completed

Treatment of Uremic Pruritus With PA101B

Uremic Pruritus

United States
Novartis Pharmaceuticals

Completed

Study of Safety, Tolerability, and Efficacy of Secukinumab in Subjects With Moderate to Severe Palmoplantar Psoriasis (GESTURE)

Moderate to Severe Palmoplantar Psoriasis

Belgium, United States, Hungary, Russian Federation, Turkey, Australia, Israel, Netherlands, Portugal, Spain, United Kingdom, Norway, Slovakia, Canada, Finland
Optinose US Inc.

Completed

12-Month OL Intranasal Fluticasone Propionate BID Using OptiNose Device

Nasal Polyps

United States
University of Rochester
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) and other collaborators

Completed

Bleach Bath Treatment of Adults With Atopic Dermatitis

Atopic Dermatitis

United States

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