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Clinical Trials/EUCTR2005-000435-18-GB
EUCTR2005-000435-18-GB
Active, not recruiting
Phase 1

Study to Determine if The Cardiovascular risk indices in Impaired Glucose Tolerance are similar for Polycystic Ovarian Syndrome, and whether they may be modified by Therapy - Cardiovascular risk in PCOS as compared to impaired glucose tolerance

niversity of Hull0 sites48 target enrollmentFebruary 25, 2005

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
This is a randomised parallel controlled trial between patients with impaired glucose tolerance and those with polycystic ovarian syndrome. Patients will either be randomised to metformin or Pioglitazone.
Sponsor
niversity of Hull
Enrollment
48
Status
Active, not recruiting
Last Updated
5 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 25, 2005
End Date
TBD
Last Updated
5 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Female

Investigators

Sponsor
niversity of Hull

Eligibility Criteria

Inclusion Criteria

  • Inclusion criteria for polycystic ovarian syndrome: Age 40\-50\.
  • Polycystic ovarian syndrome (Rotterdam consensus criteria): irregular menses since menarche, oligomenorrhoea, clinical or biochemical hyperandrogenism, polycystic ovaries on ultrasound scanning.
  • Inclusion criteria for impaired glucose tolerance:Age 40\-50
  • impaired glucose tolerance (diagnosed by WHO criteria)
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range
  • F.1\.3 Elderly (\>\=65 years) no
  • F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • Exclusion criteria for polycystic ovarian syndrome:
  • Peri\-menopausal symptoms,
  • Patient should not be on any medication, Unwilling for GP to be informed, Impaired glucose tolerance/ diabetes on GTT
  • Exclusion criteria for impaired glucose tolerance:
  • Peri\-menopausal symptoms, Patient should not be on any medication, Unwilling for GP to be informed, Polycystic ovarian syndrome (patients must have regular periods, no clinical or biochemical evidence of hyperandrogenism, normal ovaries on ultrasound scanning

Outcomes

Primary Outcomes

Not specified

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