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33 studies found for:    Open Studies | "Pruritus"
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Rank Status Study
1 Recruiting Study to Evaluate IV CR845 in Hemodialysis Patients With Moderate-to-Severe Pruritus
Condition: Uremic Pruritus
Interventions: Drug: CR845 0.5 mcg/kg;   Drug: CR845 1 mcg/kg;   Drug: CR845 1.5mcg/kg;   Drug: Placebo
2 Recruiting Study of Using Long Acting Antihistamine to Treat Opioid Induced Itching
Condition: Pruritus
Interventions: Drug: Cetirizine;   Drug: Placebo or sugar pill
3 Recruiting Pruritus and Pemphigoid in Nursing Home Patients
Conditions: Pemphigoid;   Pruritus
Intervention: Other: Blood sample
4 Not yet recruiting Central Mechanisms of Chronic Pruritus: Functional and Structural Brain Imaging.
Condition: Itch
Intervention: Other: MRI
5 Recruiting Study of the Efficacy, Safety & Tolerability of Serlopitant for Pruritus (Itch) After Burn Injury
Conditions: Pruritus;   Burns
Interventions: Drug: Serlopitant;   Drug: Placebo
6 Recruiting Efficacy of Laser Acupuncture on Pruritus in Patients With Chronic Kidney Disease Undergoing Hemodialysis
Conditions: Pruritus;   Kidney Failure, Chronic
Interventions: Device: Laser acupuncture (Olympic);   Device: Sham Laser acupuncture (Olympic)
7 Recruiting Safety, Pharmacokinetics and Preliminary Efficacy of Asimadoline in Pruritus Associated With Atopic Dermatitis
Conditions: Pruritus;   Atopic Dermatitis
Interventions: Drug: Asimadoline;   Drug: Placebo
8 Recruiting Study of the Efficacy, Safety, and Tolerability of Serlopitant for Pruritus (Itch) in Atopic Dermatitis
Conditions: Pruritus;   Atopic Dermatitis
Interventions: Drug: Serlopitant High Dose;   Drug: Placebo Oral Tablet;   Drug: Serlopitant Low Dose
9 Not yet recruiting Effect of Slow Injection of Fentanyl on the Incidence of Spinal Anesthesia Induced Itching in Cesarean Section
Condition: Itching
Interventions: Drug: (R) Rapid spinal fentanyl injection;   Drug: (S) Slow spinal fentanyl injection
10 Recruiting Neurokinin-1 Receptor Antagonist for the Treatment of Itch in EB Patients
Conditions: Epidermolysis Bullosa;   Pruritus
Interventions: Drug: VPD-737;   Drug: Placebo
11 Recruiting Tradipitant in Treatment-resistant Pruritus Associated With Atopic Dermatitis
Conditions: Atopic Dermatitis;   Eczema;   Chronic Pruritus
Interventions: Drug: Tradipitant;   Drug: Placebo
12 Recruiting Atopic Dermatitis Itch
Condition: Cutaneous Nerves CNS Itch
Interventions: Drug: Clonidine;   Drug: Naltrexone
13 Not yet recruiting Relieving Chronic Itch: Oral Medication
Condition: Pruritis
Intervention: Drug: INCB039110
14 Recruiting Ondansetron vs Ondansetron Plus Dexamethasone for Relieving Intrathecal Morphine Side Effects After C-section
Conditions: Pruritus;   Cesarean Section
Interventions: Drug: Ondansetron (Zofran);   Drug: Dexamethasone (Decadron);   Other: Spinal anesthesia
15 Not yet recruiting Dose Response Study of GSK2330672 for the Treatment of Pruritus in Patients With Primary Biliary Cholangitis
Condition: Cholestasis
Interventions: Drug: Placebo;   Drug: GSK2330672
16 Not yet recruiting Naloxone Hydrochloride Study for Relief of Pruritus in Patients With Mycosis Fungoides (MF) Form of CTCL
Conditions: Mycosis Fungoides;   Lymphoma, T-Cell, Cutaneous
Interventions: Drug: Naloxone Hydrochloride Lotion, 0.5%;   Drug: Placebo Lotion
17 Recruiting The Effect of Bezafibrate on Cholestatic Itch
Conditions: Primary Biliary Cholangitis;   Primary Sclerosing Cholangitis;   Secondary Sclerosing Cholangitis
Interventions: Drug: Bezafibrate;   Drug: Placebo
18 Recruiting Efficacy of Fluocinonide Cream 0.1% (Vanos(R)) in Reducing Itch in Subjects With Atopic Dermatitis
Condition: Atopic Dermatitis
Intervention: Drug: Fluocinonide cream
19 Recruiting Effects of Transcranial Direct Current Stimulation (tDCS) on Neuropathic Symptoms Following Burn Injury
Conditions: Burn Injury;   Chronic Pain;   Pruritus;   Itching
Intervention: Device: Transcranial direct current stimulation (tDCS)
20 Recruiting Hypnosis for Pain and Itch Following Burn Injuries
Condition: Burns
Interventions: Behavioral: Hypnosis;   Other: Standard of Care

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Study has passed its completion date and status has not been verified in more than two years.