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CARESS Study: Cabergoline for the Reduction of Endometriosis Symptoms and Lesion Size

Status
Not yet recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-522812-18-00
Enrollment
120
Registered
2025-09-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometriosis

Brief summary

Reduction in the size of endometriotic lesions assessed by transvaginal ultrasound/magnetic resonance imaging (MRI)/laparoscopy., Relief of pelvic pain measured by visual analogue scale (VAS) before and after treatment.

Detailed description

Demographic and clinical characteristics: Age, BMI, ethnicity, comorbidities (diabetes, hypertension, immunosuppression, smoking), Eznian classification (a system designed to describe deep infiltrating endometriosis (DIE) in a detailed and topographical manner, complementing the limitations of other classifications such as ASRM., Changes in serum prolactin and VEGF levels as pre- and post-treatment angiogenic markers., Impact on other symptoms associated with endometriosis, such as irregular bleeding and infertility, assessed clinically and through hormonal analysis (FSH, LH, estradiol, AMH)., Safety profile: frequency and type of adverse effects related to cabergoline (nausea, vomiting, dizziness)., Quality of life measured using specific questionnaires such as the Endometriosis Health Profile (EHP-30).

Interventions

DRUGSibilla diario 2 mg / 0
DRUG03 mg comprimidos recubiertos con película EFG
DRUGDostinex 0.5 mg Tablets

Sponsors

Hospital Clinico San Carlos
Lead SponsorOTHER

Eligibility

Sex/Gender
Male
Age
18 Years to 64 Years

Design outcomes

Primary

MeasureTime frame
Reduction in the size of endometriotic lesions assessed by transvaginal ultrasound/magnetic resonance imaging (MRI)/laparoscopy., Relief of pelvic pain measured by visual analogue scale (VAS) before and after treatment.

Secondary

MeasureTime frame
Demographic and clinical characteristics: Age, BMI, ethnicity, comorbidities (diabetes, hypertension, immunosuppression, smoking), Eznian classification (a system designed to describe deep infiltrating endometriosis (DIE) in a detailed and topographical manner, complementing the limitations of other classifications such as ASRM., Changes in serum prolactin and VEGF levels as pre- and post-treatment angiogenic markers., Impact on other symptoms associated with endometriosis, such as irregular bleeding and infertility, assessed clinically and through hormonal analysis (FSH, LH, estradiol, AMH)., Safety profile: frequency and type of adverse effects related to cabergoline (nausea, vomiting, dizziness)., Quality of life measured using specific questionnaires such as the Endometriosis Health Profile (EHP-30).

Countries

Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026