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Progesterone Suppression of Nocturnal LH Increases in Pubertal Girls (JCM017)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01773772
Recruitment Status : Active, not recruiting
First Posted : January 23, 2013
Last Update Posted : April 16, 2019
Sponsor:
Collaborator:
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Information provided by (Responsible Party):
Chris McCartney, University of Virginia

Tracking Information
First Submitted Date  ICMJE May 17, 2012
First Posted Date  ICMJE January 23, 2013
Last Update Posted Date April 16, 2019
Study Start Date  ICMJE June 2003
Actual Primary Completion Date January 2012   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: January 17, 2013)
LH pulse frequency (number of LH pulses per hour) [ Time Frame: 19 hours [from 1400 hr to 0900 hr] ]
Original Primary Outcome Measures  ICMJE Same as current
Change History
Current Secondary Outcome Measures  ICMJE Not Provided
Original Secondary Outcome Measures  ICMJE Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Progesterone Suppression of Nocturnal LH Increases in Pubertal Girls
Official Title  ICMJE Progesterone Suppression of Nocturnal LH Increases in Pubertal Girls (JCM017)
Brief Summary The purpose of this study is to learn more about how gonadotropin-releasing hormone (GnRH) and luteinizing hormone (LH) pulses are controlled during puberty. In this study, the investigators aim to discover whether or not giving 2 small doses of progesterone to early pubertal girls will prevent the nighttime increase of GnRH and LH pulses. From the information gathered in this study, the investigators may be able to learn more about how menstrual cycles are normally established in girls during puberty. Ultimately, if these normal processes can be understood, the investigators may be able to better understand abnormalities of puberty.
Detailed Description

We will recruit early pubertal, premenarcheal adolescent girls, since these stages are associated with the most prominent diurnal variations in LH pulsatility (13). Weight will be normal for height (i.e., BMI ≤ 85th and ≥ 5th percentile for age according to the CDC), and plasma testosterone will be < 40 ng/dl. We will recruit normal adolescent girls, or girls with idiopathic short stature (> 2 SD below mean height for age with no identifiable cause), from UVa Pediatric Clinics, local pediatric clinics, the Teen Health Center, and UVa Endocrine Clinics. Subjects will be late Tanner 1 (defined as having estradiol level > 20 pg/mL), Tanner 2, or Tanner 3. All potential subjects will undergo a screening history and physical prior to enrollment. These 60-90 min outpatient visits to the CRU or alternate UVA clinical unit will establish general health and developmental normality. Evaluation will include a complete personal and family medical history and physical examination (including height, weight, and pubertal stage determination using the Tanner scale). The goals and procedures of the study will be explained to potential subjects and their parents, and questions will be entertained. The volunteer and her parents will sign the assent and consent forms, respectively. Blood (20 ml) will then be drawn (at approx. 0800-0900 h) for the following tests: LH, FSH, P, E2, total testosterone, SHBG, DHEA-S, 17-OHP, beta-hCG, TSH, CBC, chemistry and liver panels, prolactin, insulin, Insulin-like Growth Factor 1 (IGF-1), and cytokines and adipokines (including adiponectin, leptin, resistin, PAI-1, IL-1b, IL-6, IL-8, TNFa, MCP-1, HGF and NGF). Subjects will need to fast for a minimum of 8 hours prior to screening blood draw. Bone age (plain x-ray of left hand and wrist) will also be performed as a marker of biological age, since pubertal stage generally correlates better with bone age than chronological age.

If the screening labs show a hemoglobin < 11.0g/dL for African American subjects or hemoglobin < 11.5 g/dL for non-African American subjects, iron therapy at a dose of 1-2 mg/kg will be encouraged for 60 days. Subjects weighing ≤ 36 kg will be given 300-325 mg oral ferrous gluconate daily (containing 36 mg of elemental iron); subjects weighing > 36 kg will be given 300-325 mg oral ferrous gluconate twice daily. Hemoglobin will then be rechecked in the CRU or clinical unit; if acceptable (hemoglobin ≥ 11 g/dL for African American subjects or hemoglobin ≥ 11.5 g/dL for non-African American subjects), the inpatient admission will be scheduled.

If the screening labs are normal, iron supplementation at a dose of 1-2 mg/kg for 30 days will be given to help prevent anemia from developing during the study. Subjects weighing ≤ 36 kg will be given 300-325 mg oral ferrous gluconate daily (containing 36 mg of elemental iron); subjects weighing > 36 kg will be given 300-325 mg oral ferrous gluconate twice daily.

If safety labs are abnormal during screening (e.g., abnormal liver tests, abnormal TSH), subjects will be asked to return once for repeat (confirmatory) labs to exclude lab error. Repeat testing will generally occur within one month of the original screening lab draw. If exclusionary lab values are confirmed on such repeat testing, subjects will be excluded from participation.

1-3 days before overnight admission: An outpatient blood sample will be obtained 1-3 d before overnight admission. Plasma P will be checked to exclude an unlikely luteal phase, with overnight admission cancelled if P exceeds 1.5 ng/ml. Hemoglobin will be obtained if these have not been obtained within 30 days of the overnight admission (subsequent overnight admission cancelled if hemoglobin < 11 g/dl for African American subjects or < 11.5 g/dL for non-African American subjects). Urine beta-HCG will be assessed to exclude pregnancy. If three months have elapsed between an overnight admission and the subject's most recent safety labs, then additional safety labs (chemistry and liver panel) will be obtained at this time.

Inpatient Admission: Subjects will be admitted to the CRU, alternate UVA hospital unit, or off-site hotel at 1400 h. In general, parents are welcome to stay with their child at the off-site hotel if they wish. If the overnight portion of the study is to be done at an off-site hotel, the subject may stay without a parent or legal guardian, as long as two CRU staff are present. Whether or not a parent needs to remain during the overnight admission will be discussed when the visit is scheduled. An i.v. line with be placed in the forearm vein (this may be facilitated by EMLA cream), on the same side as the dominant hand if possible. Subjects will take 25-50 mg oral micronized P or placebo at 1600 h and again at 2000 h. P dosing will be based on weight, with 25 mg administered to girls < 42 kg and 50 mg given to those ≥ 42 kg; with P administration, we aim to produce mean P concentrations of approximately 2-3 ng/ml. Frequent blood sampling will begin at 1900 h and continue for 14 h as follows: LH every 10 min (1 ml); and FSH every 10 min (no additional blood required); P, E2, T, DHEA and cortisol every 30 min (1 ml). An additional 0.3 cc sample will be drawn at 0700 to test for fasting glucose. Fasting insulin, SHBG, estrone, androstenedione, DHEA-S will be performed on pooled samples from 05:00-07:00.

Lights will be extinguished at 2200 h to facilitate sleep, which will be carefully recorded by trained observers. During blood sampling, activity (e.g. awake, sleeping) will be recorded by the nurse every 10 minutes. Additionally, periods of sleep will be estimated using wrist actigraphy (Motionlogger Basic-L; Ambulatory Monitoring, Inc.) The Motionlogger Basic-L is a watch-like device (that includes an accelerometer) that will be worn on the non-dominant wrist by the research participant during the overnight admission. There will be an overnight fast from 22:00 until 07:00. Subjects will be awakened at 0700 h. Sampling will cease at 0900 h.

During the admission, ~150 ml of blood will be drawn (including 0.25 ml discarded with each sample). The total amount of blood that will be drawn during the study, including the screening, outpatient P sampling, and inpatient admission is ~170 ml. One of the parents will be allowed to stay overnight with the subject during the admission. After the last sample is taken, volunteers will be discharged on oral iron supplementation to be taken for 30 d.

Follow-up:

We will advance every effort to follow subjects (via outpatient CRU or clinic visits) at 6- to 12-month intervals for up to 3 y to assess progression of puberty, onset and frequency of menses, and development of signs of hyperandrogenism (e.g., hirsutism). We will obtain blood for LH, FSH, E2, P, and T during these follow-up visits. These follow-up visits will be encouraged, but not mandatory.

Study Type  ICMJE Interventional
Study Phase  ICMJE Phase 1
Study Design  ICMJE Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: Single (Participant)
Primary Purpose: Basic Science
Condition  ICMJE Female Puberty
Intervention  ICMJE
  • Drug: Progesterone
    Subjects will take 25-50 mg oral micronized progesterone at 1600 h and again at 2000 h. Progesterone dosing will be based on weight, with 25 mg administered to girls < 42kg and 50 mg given to those or = to 42 kg.
  • Drug: Placebo
    Subjects will take oral placebo suspension at 1600 h and again at 2000 h.
Study Arms  ICMJE
  • Experimental: Progesterone
    Subjects will take 25-50 mg oral micronized P or placebo at 1600 h and again at 2000 h. P dosing will be based on weight, with 25 mg administered to girls < 42kg and 50 mg given to those > or = 42 kg.
    Intervention: Drug: Progesterone
  • Placebo Comparator: Placebo
    Subjects will take placebo at 1600 h and again at 2000 h.
    Intervention: Drug: Placebo
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Active, not recruiting
Estimated Enrollment  ICMJE
 (submitted: January 17, 2013)
24
Original Estimated Enrollment  ICMJE Same as current
Estimated Study Completion Date  ICMJE December 2019
Actual Primary Completion Date January 2012   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  • Female volunteers in early to mid-puberty (i.e. late Tanner 1 [estradiol level >20 pg/ml], Tanner 2, or Tanner 3)
  • Premenarcheal

Exclusion Criteria:

  • BMI-for-age > 85th percentile or < 5th percentile
  • Pregnancy
  • Inability to comprehend what will be done during the study or why it will done
  • Hyperandrogenism (e.g., hirsutism, elevated free testosterone level)
  • History of allergy to progesterone (which is extremely rare)
  • Hemoglobin less than 12 g/dl and hematocrit less than 36%
  • Persistently abnormal sodium, potassium, or bicarbonate (i.e. confirmed on repeat)
  • Persistently elevated creatinine, hepatic transaminases, or alkaline phosphatase (i.e., confirmed on repeat)
  • Total bilirubin > 1.5 times upper limit of normal (i.e. confirmed on repeat)
  • Significant history of cardiac or pulmonary dysfunction (e.g., known or suspected congestive heart failure; asthma requiring intermittent systemic corticosteroids; etc.)
  • Untreated hypo- or hyperthyroidism, reflected by persistently abnormal thyroid-stimulating hormone (TSH) values
  • Premature adrenarche (i.e., occurring before age 8 y)
  • Basal (follicular) 17-hydroxyprogesterone > 200 ng/ml (confirmed on repeat)
  • Dehydroepiandrosterone-sulfate (DHEA-S) > age-appropriate upper limit of normal (confirmed on repeat)
  • Hyperprolactinemia (confirmed on repeat)
  • Weight less than 25 kg
Sex/Gender  ICMJE
Sexes Eligible for Study: Female
Ages  ICMJE 9 Years to 14 Years   (Child)
Accepts Healthy Volunteers  ICMJE Yes
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE United States
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT01773772
Other Study ID Numbers  ICMJE 10504
U54HD028934 ( U.S. NIH Grant/Contract )
P50HD028934 ( U.S. NIH Grant/Contract )
Has Data Monitoring Committee No
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement  ICMJE
Plan to Share IPD: Undecided
Plan Description: We do not have current plans to share IPD
Responsible Party Chris McCartney, University of Virginia
Study Sponsor  ICMJE University of Virginia
Collaborators  ICMJE Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Investigators  ICMJE
Principal Investigator: Christopher R. McCartney, MD University of Virginia
PRS Account University of Virginia
Verification Date April 2019

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