Skip to content

comparison of cabergolin with Sandostatin lar plus cabergolin in treatment of nonfunctional pituitary adenomas

comparison of cabergolin with Sandostatin lar plus cabergolin in size reduction of nonfunctional pituitary adenomas after surgery :an open label clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171003036521N2
Enrollment
30
Registered
2018-03-12
Start date
2018-04-04
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

nonfunctional pituitary adenoma. Pituitary gland

Interventions

Intervention 1: Grupe 1 or intervention , will receive sandostatin lar 20 mg q 28 day plus cabergolin 3 – 7 mg per week for 6 months.Cabeergolin frome OSVE company and Sandostatin lar frome NOVARTIS

Sponsors

Iran University of Medical Sciences
Lead Sponsor
Gorgan University of Medical Sciences
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with NFPAs that don't cured by surgery and are SSR –R 1-5 positive ,who have less than 80% resection rate after surgery Patient with NFPAs and are SSR –R 1-5 positive ,that patient who have tumor regrowth after surgery Patient with NFPAs and are SSR –R 1-5 positive ,who previously didn't have received radiotherapy Patient with NFPAs and are SSR –R 1-5 positive ,who previously didn't have received medical therapy with dopamine agonists or somatostatin analogues Patient with NFPAs who don't , SSR –R 1-5 positive

Exclusion criteria

Exclusion criteria: Patients with NFPAs that have cured by surgery ,who have more than 80% resection rate after surgery Patient with NFPAs and , who have emergency surgical indication Patient with NFPAs , who previously have received radiotherapy Patient with NFPAs who have emergency surgical indication Patient with NFPAs ,who previously have received medical therapy with dopamine agonists or somatostatin analogues

Design outcomes

Primary

MeasureTime frame
Non functional pituitary adenoma size. Timepoint: Non functional pituitary adenoma size before and 6 months after treatment. Method of measurement: Adenoma size in MRI.

Secondary

MeasureTime frame
Secondary Hypothyroidism. Timepoint: Before and 3 , 6 months after treatment. Method of measurement: Measurement OF T3 ,T4, TSH , Blood sample.;Adrenal insufficiency. Timepoint: Before and 3 , 6 months after treatment. Method of measurement: Serum Cortisol level, blood sample.;Visual field. Timepoint: Before and 6 months after treatment. Method of measurement: Primetry.;Panhypopituitarism. Timepoint: Before and 3 , 6 months after treatment. Method of measurement: Pituitary hormonal assessment in blood sample.;Hypogonadism. Timepoint: Before and 3 , 6 months after treatment. Method of measurement: Measurement LH,FSH ,Esradiol in women and LH,FSH,Testosterone in men, Blood sample.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamideh Akbari

Gorgan University of Medical Sciences

akbari.ha@iums.ac.ir+98 17 3242 1651

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026