Clomiphene Citrate for Treatment of Acromegaly
Primary Purpose
Acromegaly
Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Clomiphene Citrate
Sponsored by
About this trial
This is an interventional treatment trial for Acromegaly focused on measuring Acromegaly, SERM, Clomiphene
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.
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
NCT ID
NCT02274311
First Posted
October 20, 2014
Last Updated
April 15, 2019
Sponsor
Felipe Henning Gaia Duarte
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
Learn more about this trial
Clomiphene Citrate for Treatment of Acromegaly
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