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Clomiphene Citrate for Treatment of Acromegaly

Primary Purpose

Acromegaly

Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Clomiphene Citrate
Sponsored by
Felipe Henning Gaia Duarte
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acromegaly focused on measuring Acromegaly, SERM, Clomiphene

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • patients with active acromegaly on regular use of a stable dose of Octreotide-LAR and/or cabergoline for at least one year,
  • Insulin like growth factor 1 above the reference range during the last year of follow-up and
  • testosterone levels within or below the third inferior tertile of normality.

Exclusion Criteria:

  • radiotherapy in the last 10 years, previous venous embolism (including family members),
  • previous prostatic cancer or symptomatic benign hypertrophy,
  • triglyceride levels above 400 mg/dL,
  • renal failure defined by estimative of renal filtration below 30 ml/min,
  • liver disease defined by hepatic enzymes 3 times above normal limit,
  • active oncologic disease in the last 10 years and previous cardiac or cerebrovascular disease.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Clomiphene citrate

    Arm Description

    Patients receiving clomiphene citrate

    Outcomes

    Primary Outcome Measures

    IGF-1 Levels
    The objective is to compare the change of IGF-1 value assessed in the beginning of the study (day 0), with the value obtained after three months of use of clomiphene citrate (day 90).

    Secondary Outcome Measures

    Testosterone Levels
    The objective is to compare the change of testosterone value assessed in the beginning of the study (day 0), with the value obtained after three months of use of clomiphene citrate (day 90).
    PSA Levels
    The objective is to compare the change of PSA value assessed in the beginning of the study (day 0), with the value obtained after three months of use of clomiphene citrate (day 90).

    Full Information

    First Posted
    October 20, 2014
    Last Updated
    April 15, 2019
    Sponsor
    Felipe Henning Gaia Duarte
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02274311
    Brief Title
    Clomiphene Citrate for Treatment of Acromegaly
    Official Title
    Clomiphene Citrate for Treatment of Acromegaly Not Controlled by Conventional Therapies
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2019
    Overall Recruitment Status
    Completed
    Study Start Date
    January 2011 (undefined)
    Primary Completion Date
    October 2014 (Actual)
    Study Completion Date
    October 2014 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Felipe Henning Gaia Duarte

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    To assess the impact of clomiphene citrate on serum insulin like growth factor 1 and testosterone levels in male acromegalic patients not controlled by surgery, radiotherapy and/or medical treatments (somatostatin analogues, dopamine agonists and/or growth hormone receptor antagonist)
    Detailed Description
    Acromegaly, a disease caused by a growth hormone secreting pituitary adenoma, results in reduced life span. Despite the many modalities available to treat this disease,as surgery, medical treatment and radiotherapy, uncontrolled disease persists in a significant portion of patients Oral estrogens, alone or in combination with somatostatin receptor analogues, have been shown to control acromegaly in women. Selective estrogen receptor modulators (SERMs) resulted in similar effects in both genders. Clomiphene citrate, a SERM that increases luteinizing hormone and follicle stimulating hormone secretion, improves hypogonadism and fertility outcomes. The aim of this study is to assess the impact of clomiphene citrate on serum insulin like growth factor 1 and testosterone levels in male acromegalic patients not controlled by surgery, radiotherapy and/or medical treatment. In this prospective, open label, single center trial, sixteen male patients were studied. Clomiphene citrate (50 mg/day) was added to previous medical treatment for 3 months and hormonal assessment was performed prior to and during the intervention. Hormones included: growth hormone, insulin like growth factor, total testosterone, follicle stimulating hormone, luteinizing hormone and prostate-specific antigen.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Acromegaly
    Keywords
    Acromegaly, SERM, Clomiphene

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    16 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Clomiphene citrate
    Arm Type
    Experimental
    Arm Description
    Patients receiving clomiphene citrate
    Intervention Type
    Drug
    Intervention Name(s)
    Clomiphene Citrate
    Other Intervention Name(s)
    Clomid; Serophene; Indux
    Intervention Description
    Clomiphene citrate, 50 mg, orally for three months
    Primary Outcome Measure Information:
    Title
    IGF-1 Levels
    Description
    The objective is to compare the change of IGF-1 value assessed in the beginning of the study (day 0), with the value obtained after three months of use of clomiphene citrate (day 90).
    Time Frame
    Day 90
    Secondary Outcome Measure Information:
    Title
    Testosterone Levels
    Description
    The objective is to compare the change of testosterone value assessed in the beginning of the study (day 0), with the value obtained after three months of use of clomiphene citrate (day 90).
    Time Frame
    D90
    Title
    PSA Levels
    Description
    The objective is to compare the change of PSA value assessed in the beginning of the study (day 0), with the value obtained after three months of use of clomiphene citrate (day 90).
    Time Frame
    Day 90

    10. Eligibility

    Sex
    Male
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: patients with active acromegaly on regular use of a stable dose of Octreotide-LAR and/or cabergoline for at least one year, Insulin like growth factor 1 above the reference range during the last year of follow-up and testosterone levels within or below the third inferior tertile of normality. Exclusion Criteria: radiotherapy in the last 10 years, previous venous embolism (including family members), previous prostatic cancer or symptomatic benign hypertrophy, triglyceride levels above 400 mg/dL, renal failure defined by estimative of renal filtration below 30 ml/min, liver disease defined by hepatic enzymes 3 times above normal limit, active oncologic disease in the last 10 years and previous cardiac or cerebrovascular disease.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Marcello D Bronstein, MD, PhD
    Organizational Affiliation
    Unit of Neuroendocrinology, Discipline of Endocrinology, Department of Internal Medicine Clinical Hospital of the University of São Paulo Medical School, São Paulo, Brazil
    Official's Role
    Study Chair

    12. IPD Sharing Statement

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    Clomiphene Citrate for Treatment of Acromegaly

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