Clinical trials

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

Condition / disease
Location
Status: Recruiting

Efficacy and Tolerability of Sucrosomial® Iron vs Ferric Maltol in Iron Deficient Women

This study aims to compare two oral iron treatments, Sucrosomial® Iron and Ferric Maltol, in women with mild to moderate iron deficiency anemia. Many patients experience gastrointestinal side effects or poor tolerability with traditional iron supplements, which may limit adherence. Participants will be randomly assigned to receive either Sucrosomial® Iron or Ferric Maltol for 12 weeks. The primary objective is to determine whether Sucrosomial® Iron is as effective as Ferric Maltol in normalizing hemoglobin levels.

Participants needed: 146
Trial details
Phase: Phase 4Age: 18+Biological sex: FemaleType: InterventionalSponsor: Pharmanutra S.p.a.Updated: Sep 3, 2026Locations: 7
Eligibility criteria

Female participants ≥ 18 years [+2]

Use of iron-containing drugs or supplements within 1 month prior to screening [+13]

Status: Recruiting

Effect of a Food for Special Medical Purposes on Muscle Mass Preservation During GLP-1 RAs Weight Loss Treatment

This study evaluates whether a Food for Special Medical Purposes (FSMP) can help to preserve appendicular skeletal muscle mass (ASMM) in adults undergoing weight loss treatment with GLP-1 receptor agonists or dual GIP/GLP-1 receptor agonists. Participants will receive the FSMP or a matching placebo for 24 weeks while continuing standard GLP-1-based therapy. ASMM will be measured using Bioelectrical Impedance Vector Analysis (BIVA).

Participants needed: 144
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Pharmanutra S.p.a.Updated: Mar 23, 2026Locations: 3
Eligibility criteria

Age ≥18 years and ≤ 65 years old; [+5]

Type I and Type II diabetes; patients with pre-diabetes and/or metabolic syndrom... [+8]

Status: Recruiting

Oral Supplementation With a Formulation Based on Cetylated Fatty Acids for Post-fracture Long Bone Healing

This clinical study aims to evaluate the potential benefits of a formulation based on Cetylated Fatty Acids in improving fracture healing of long bones in the lower limbs. The investigational product is administered orally over a 12-week period. Study procedures are limited to standard imaging techniques (radiography and echography), blood sampling, and completion of validated quality of life questionnaires.

Participants needed: 100
Trial details
Age: 18-85Biological sex: AllType: InterventionalSponsor: Pharmanutra S.p.a.Updated: Dec 23, 2025Locations: 6
Eligibility criteria

Between 18 and 85 years old [+6]

Treatment with vitamin D for medical purpose (Non-union, osteoporosis…) [+22]