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

Evaluation of Adherence With Bisphosphonates and Calcium and Vitamin D Supplements in Women With Postmenopausal Osteoporosis

This study aims to evaluate the adherence of patients to combined treatment with bisphosphonates and calcium and vitamin D supplements, which is one of the usual treatments for postmenopausal osteoporosis. The study will consist of a single visit that will coincide with one of the patient's usual follow-up visits according to standard clinical practice. During this visit, information will be collected from the patient's medical history and an interview will be conducted using 3 questionnaires to assess how and how often the patient takes the treatment, possible forgetfulness, and whether or not the patient is satisfied with their current treatment.

Participants needed: 480
Trial details
Biological sex: FemaleType: ObservationalSponsor: Procare Health Iberia S.L.Updated: Aug 5, 2025Locations: 21
Eligibility criteria

- Women diagnosed with postmenopausal OP. [+2]

Status: Recruiting

Observational Study to Evaluate Fertility in Women Between 32 and 38 Years Old Treated With the Ovosicare® Fertility

The goal of this observational study is to evaluate whether supplementation with the Ovosicare® Fertility food supplement increases the possibility of becoming pregnant in women aged between 32 and 38 years who have been trying to become pregnant for at least 6 months before starting supplementation.

Participants needed: 300
Trial details
Age: 32-38Biological sex: FemaleType: ObservationalSponsor: Procare Health Iberia S.L.Updated: Jul 24, 2025Locations: 27
Eligibility criteria

- Women who agree to participate in the study by signing the informed consent. [+2]

- BMI > 30 kg/m2. [+13]

Status: Recruiting

A Multicenter, Open, Comparative Study on Vaginal Dysbiosis in Premenopausal Women (DISPALOMA)

The hypothesis is raised of improving the status of vagnal microbiota with a non-hormonal topical product in early situations of dysbiosis in which the vaginal pH is elevated and the patient may or may not be symptomatic, in order to try to prevent the appearance of future established vaginal infections.

Participants needed: 30
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Procare Health Iberia S.L.Updated: Feb 3, 2025Locations: 2
Eligibility criteria

Between 18 and 45 years of age, inclusive. [+4]

Diagnosis of another vaginal or vulvar condition that may confuse the interpreta... [+11]