CClinicalTrials.gg
Status unknownNCT01459601Updated Oct 25, 2011

Cabergoline Effect on Blood Sugar in Type 2 Diabetics

An interventional study of Cabergoline in Diabetes Type 2, sponsored by Mashhad University of Medical Sciences. Status unknown. Per ClinicalTrials.gov, last updated 2011-10-25.

Sponsored by Mashhad University of Medical Sciences · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Oct 2011), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
10
Allocation
Randomized
Sex
All
01

Study summary

Diabetic patients with poorly control blood sugar are prescribed cabergoline for 1 months and their blood glucose is evaluated.

02

Conditions studied

  • Diabetes Type 2

Keywords

  • diabetes mellitus
  • FBS
  • HbA1C
  • Cabergoline
03

In context

Diabetes Mellitus, Type 2

9,359 studies on the registry are indexed under Diabetes Mellitus, Type 2; 1,318 are open to participants now.

This study's planned enrollment of 10 is below the median of 80 across 7,525 interventional studies indexed under Diabetes Mellitus, Type 2.

Browse Diabetes Mellitus, Type 2 studies →

Lead sponsor

Mashhad University of Medical Sciences is the lead sponsor of 90 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Type 2 diabetes
  • HbA1C>7

Exclusion criteria

Exclusion Criteria:

  • HbA1C>10
  • Psychiatric disorders
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Single group
Masking
Single (Participant)
Enrollment
10 participants (estimated)

Interventions

  • DrugCabergoline

    0,5mg per week

    Also known as: Dastinex

06

What researchers measure

Primary outcomes

  1. FBS (fasting blood sugar)

    Time frame: 30days

Secondary outcomes

  1. HbA1C

    Time frame: 30days

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 25, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01459601
Lead sponsor
Mashhad University of Medical Sciences
Responsible party
Haleh Rokni Yazdi (assisstant professor, Mashhad University of Medical Sciences) — Principal investigator
First posted
Oct 25, 2011
Start date
Jan 2012
Primary completion
Feb 2012 (estimated)
Completion
Feb 2012 (estimated)
Last update
Oct 25, 2011

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2011. You cannot join it, but the record below documents what was studied.

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