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Trial Search

Current Search Criteria:

Intervention: Sodium lauryl sulfate

Found 94 matching trials

Study of New Tablet Formulations and Suspension Formulation Compared to Current (1B) Formulation of BILR 355 BS in Healthy Male Volunteer Subjects

PHASE1

1. To investigate the relative bioavailability (BA) of improved tablet form...

Status

Completed

Location

Multiple Locations

Start Date

2005-06

Trial ID

NCT02259868

Treatments Being Tested

BILR 355 BS /1B, current low dose formulation BILR 355 BS /1B, current high dose formulation BILR 355 BS - Jet Milled (JM) + Sodium Dodecyl Sulfate (SDS) formulation BILR 355 BS - Hammer Milled (HM) + Sodium Dodecyl Sulfate (SDS) formulation BILR 355 BS - Suspension low dose BILR 355 BS - Suspension high dose Ritonavir

Study to Determine Skin Irritation Potential of an Antifungal Cream Containing Trolamine After Repeated Skin Application (Cumulative Irritation Patch Test)

PHASE3

In this study researchers want to study the potential skin reaction after r...

Status

Completed

Location

Multiple Locations

Start Date

2013-06-10

Trial ID

NCT04531813

Treatments Being Tested

Butenafine HCl 1% (BAY1896425)Positive Control-Sodium lauryl sulfate (SLS)Negative Control

A Study to Evaluate the Skin Irritation Potential of PBI-100 Topical Cream in Healthy Participants

PHASE1

This is an open-label, single-arm, randomized, evaluator-blinded repeat ins...

Status

Completed

Location

KGL Skin Study Center

Start Date

2021-04-12

Trial ID

NCT04882631

Treatments Being Tested

PBI-100 Topical Cream Positive Control - Sodium laurel sulfate (SLS)PBI-100 Topical Cream, Vehicle Negative Control

An Study to Investigate the Recovery, Excretion, and Pharmacokinetics of 14C-GSK1265744 Administered as a Single Oral Dose and a Study to Describe the Pharmacokinetics of a Supratherapeutic Dose of GSK1265744 in Healthy Adult Subjects

PHASE1

This will be a two-part study in healthy adults. Part A is a phase 1, non-r...

Status

Completed

Location

GSK Investigational Site

Start Date

2013-05

Trial ID

NCT01848340

Treatments Being Tested

GSK1265744B (sodium salt) containing 14C-GSK1265744B 150 mg GSK1265744B Placebo

Cryosurgery and Cream Combination for Actinic Keratosis

PHASE3

Carac 0.5% cream is approved for daily topical treatment of AK's for up to ...

Status

Completed

Location

Wake Forest University Health Sciences Department of Dermatology

Start Date

2011-01-05

Trial ID

NCT03037541

Treatments Being Tested

Carac Cream Placebo Cetaphil cream

Safety Study to Evaluate the Cumulative Irritation Potential of Topically Applied ZuraPrep™ and ZuraPrep™ Without IPA

PHASE1

This is a safety study to determine the cumulative skin irritation potentia...

Status

Completed

Location

BioScience Laboratories

Start Date

2014-06

Trial ID

NCT02160574

Treatments Being Tested

ChloraPrep 0.1% Sodium Lauryl Sulfate 0.9% Physiological Saline ZuraPrep without IPA

Skin Sensitisation (Modified Draize-95 Test)

Skin Sensitization Test (Modified Draize-95) to Support a Low Dermatitis Po...

Status

Completed

Location

Makmal Bioserasi & Klinikal, Healthmedic Research Sdn. Bhd.

Start Date

2019-11-23

Trial ID

NCT04402476

Treatments Being Tested

Powder Free Polychloroprene Surgical Gloves, Sterile. Low Dermatitis Potential, tested for use with Chemotherapy drugs.

Dosing, Safety and Pharmacokinetic Profile of Rifabutin in Children Receiving Concomitant Treatment With Kaletra

PHASE1

Open label pharmacokinetic RBT dose-finding study in young (≤ 5 year old) H...

Status

Unknown

Location

Harriet Shezi Children's Clinic, Chris Hani Baragwanath Hospital, WHI, University of the Witwatersrand

Start Date

2010-11

Trial ID

NCT01259219

Treatments Being Tested

Mycobutin

Skin Safety Study to Evaluate the Sensitizing Potential in Healthy Volunteers

PHASE1

This is a single center, randomized, controlled, within subject comparison,...

Status

Completed

Location

TKL research

Start Date

2014-09

Trial ID

NCT02256930

Treatments Being Tested

M518101 M518101 Vehicle Sodium lauryl sulfate Saline

Cotrimoxazole Prophylaxis Cessation Study Among Stabilized HIV-Infected Adult Patients on HAART in Entebbe, Uganda

PHASE4

According to the national guidelines in Uganda and to the World Health Orga...

Status

Unknown

Location

MRC/UVRI Uganda Research Unit on Aids

Start Date

2008-06

Trial ID

NCT00674921

Treatments Being Tested

cotrimoxazole Placebo

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