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The Safety and Efficacy of Recombinant Human Prolactin
This study has been completed.
Study NCT00438490   Information provided by Massachusetts General Hospital
First Received: February 20, 2007   Last Updated: February 21, 2007   History of Changes

February 20, 2007
February 21, 2007
April 2002
 
Galactorrhea
Same as current
Complete list of historical versions of study NCT00438490 on ClinicalTrials.gov Archive Site
  • Bone Turnover-deoxypyridinoline, N-telopeptide, bone specific Alkaline Phosphatase
  • Menstrual cycle length
  • Reproductive hormones-LH, FSH, Estradiol
Same as current
 
The Safety and Efficacy of Recombinant Human Prolactin
Phase 2 Study of Recombinant Human Prolactin Efficacy and Safety

Medications used to increase breast milk production increase prolactin secretion, the main hormone of lactation. There are no FDA approved medications used to improve breast feeding, but metoclopramide is used off-label and can have intolerable side effects. We examined the biological activity and safety of recombinant human prolactin (r-hPRL) as a potential medication to augment lactation. In this study, the effect of r-hPRL on breast milk production in women who did not recently deliver a baby and its effect on the bones and menstrual cycle were tested.

There are no FDA approved medications in the U.S. to augment lactation. Metoclopramide is used off-label but can have intolerable side effects. We examined the biological activity and safety of recombinant human prolactin (r-hPRL) as preliminary data for its use to augment lactation. Healthy, non-postpartum women (n=21) with regular menstrual cycles underwent a 7 day randomized, double-blind, placebo-controlled trial of r-hPRL. Galactorrhea, markers of bone turnover, calcium homeostasis and gonadal function were measured and side effects recorded.

Phase II
Interventional
Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Healthy
Drug: Recombinant Human Prolactin
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
20
December 2003
 

Inclusion Criteria:

Healthy Subjects will meet the following criteria:

  1. 18 to 40 years of age
  2. Normal weight (BMI 17 to £ 30 kg/m2)
  3. Good general health
  4. On no medications for at least 3 months before the study
  5. Regular menstrual cycles every 25-35 days with ovulation documented by a luteal phase progesterone level
  6. No evidence of androgen excess
  7. Normal TSH, prolactin and hematocrit
  8. No current interest in conception
  9. No history of osteoporosis
  10. No use of medications known to affect bone turnover
  11. No alcoholism
  12. No smoking
  13. No history of medical problems or treatment known to affect bone turnover.

Exclusion Criteria:

Subjects will be excluded for pregnancy or evidence of breast masses.

Female
18 Years to 40 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00438490
 
2001-P-001057
Massachusetts General Hospital
 
Principal Investigator: Corrine K. Welt, MD Massachusetts General Hospital
Massachusetts General Hospital
February 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP