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The PROMISE Survey

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University Hospital Basel

Status

Active, not recruiting

Conditions

Prolactinoma
Pituitary Tumor

Study type

Observational

Funder types

Other

Identifiers

NCT06936813
2025-00327 kt25Atila2;

Details and patient eligibility

About

The PROMISE Survey was developed to systematically assess the real-world experiences, treatment preferences, side effects, and outcomes from both patients and physicians dealing with prolactinomas. The aim is to generate insights that can guide future clinical research and improve individualized care strategies.

Full description

Background

Prolactinomas are the most common hormone-producing pituitary tumors, causing symptoms like menstrual irregularities, infertility, galactorrhea, and reduced libido due to elevated prolactin levels. The standard treatment involves dopamine agonists (DAs) such as cabergoline or bromocriptine, which are usually effective. However, many patients report side effects (e.g., nausea, dizziness, psychiatric symptoms), leading to challenges in long-term adherence and uncertainty about outcomes after discontinuing therapy. Surgical treatment has emerged as a potentially safe and effective alternative, especially for selected patients, but perspectives from both patients and physicians on treatment preferences and outcomes are not well studied.

The survey is designed to be completed in 5-10 minutes, fostering high participation across diverse patient and physician populations. Data are collected anonymous covers the following areas:

  1. Patient Characteristics
  2. DA Therapy
  3. Surgical Treatment
  4. Diagnostic Pathway
  5. Treatment Side Effects & Recurrence
  6. Quality of Life and Psychosocial Impact
  7. Physician Perspectives
  8. Knowledge Gaps
  9. Hypothesis Generation

Outcome

The collected data will inform:

  • Better understanding of real-world management and challenges in prolactinoma care.
  • Insights for improving clinical guidelines, patient education, and treatment decision-making.
  • Hypotheses for future studies comparing outcomes of DA therapy vs. surgery and optimizing long-term management strategies.

Enrollment

530 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Prolactinoma patients
  • Prolactinoma treating physicians including endocrinologists and neurosurgeons

Trial contacts and locations

1

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Central trial contact

Cihan Atila, MD

Data sourced from clinicaltrials.gov

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