Health Trials

Clinical trials

5

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Study to Evaluate Ibuprofen (IBU) 62.5 mg and Acetaminophen (APAP) 125 mg/5 ml in an Oral Liquid Suspension Fixed-Dose Combination Product in Children Aged 6 to 11 Years

The purpose of this study will be to characterize the pharmacokinetic (PK) profile of the Fixed-Dose Combination (FDC) IBU 62.5 milligram (mg)/APAP 125 mg per 5 milliliter (mL) suspension in children 6 to 11 years of age, inclusive, to satisfy Pediatric Research Equity Act (PREA) requirements.

Participants needed: 12
Trial details
Phase: Phase 1Age: 6-11Biological sex: AllType: InterventionalSponsor: HALEONUpdated: Jun 30, 2026Locations: 1
Eligibility criteria

Participant with at least one acute, painful condition (e.g., minor aches and pa... [+9]

Participants with evidence or history of clinically significant hematological, r... [+21]

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Status: Recruiting

A Study Evaluating Oral-Health-Related Quality of Life and Treatment Patterns Among Dentin Hypersensitivity Sufferers

The primary purpose of this study is to characterize changes in Oral-Health-Related Quality of Life (OHrQoL), as measured by the Dentin Hypersensitivity Experience Questionnaire (DHEQ) over a 12-month period.

Participants needed: 375
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: HALEONUpdated: Apr 28, 2026Locations: 1
Eligibility criteria

Participant who has provided consent indicating they have been informed of all p... [+5]

Anyone who has any chronic health conditions that could impact their participati... [+8]

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Status: Recruiting

A Clinical Study to Assess the Effectiveness of Use of Three Experimental Denture Adhesives Compared to Using No-Adhesive

The aim of the proposed clinical study is to investigate the efficacy of three experimental denture adhesive creams to improve denture hold over a period of 13 hours.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: HALEONUpdated: Apr 9, 2026Locations: 1
Eligibility criteria

Participant provision of a signed and dated informed consent document indicating... [+6]

A participant who is an employee of the investigational site, either directly in... [+10]

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Status: Recruiting

Real-World Study of a Calcium Sodium Phosphosilicate Anti-Sensitivity Toothpaste for Dentin Hypersensitivity Relief

The aim of this study is to evaluate the impact of a commercially available desensitizing dentifrice containing 5 percent (%) Calcium sodium phosphosilicate (CSPS) on oral health related quality of life (OHrQoL) in a DH (Dentin Hypersensitivity) population in a real-world setting.

Participants needed: 500
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: HALEONUpdated: Mar 11, 2026Locations: 1
Eligibility criteria

Participant who has provided consent indicating they have been informed of all p... [+3]

Participant who has been/is on multiple prescription medications to treat severe... [+6]

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Status: Recruiting

A Clinical Study to Evaluate the Effectiveness of an Experimental Toothpaste in Improving Gum Health and Reducing Plaque Accumulation

The aim of this 24-week clinical study is to evaluate the ability of an experimental dentifrice containing 0.454 percent (%) weight by weight (w/w) Stannous fluoride (SnF2); to improve gingival health, plaque reduction and prevention of plaque accumulation compared with a regular fluoride dentifrice (negative control) in participants with mild to moderate gingivitis.

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: HALEONUpdated: Dec 19, 2025Locations: 1
Eligibility criteria

Participant provision of a signed and dated informed consent document indicating... [+3]

A participant who is an employee of the investigational site, either directly in... [+22]

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