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临床试验/NCT02431416
NCT02431416已完成不适用

Effect of a GnRH Injection on Ghrelin Concentrations in Girls With Suspected Precocious Puberty

Region Örebro County1 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2015年5月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
13
试验地点
1
主要终点
Ghrelin concentration after GnRH injection and after saline injection

研究概览

简要总结

The purposes of the study is to investigate whether circulating levels of ghrelin decreases after an iv injection of GnRH in girls with suspected central premature puberty and to investigate the effects of different post sampling handling on the preservation of acylated ghrelin.

详细描述

Patients with clinically suspected central premature puberty undergo a GnRH stimulation test to have an appropriate diagnosis. 20 such girls will be recruited to this study and a modified GnRH stimulation test will be done. The modification includes prolonged blood sampling time (0, 30, 60, 90, 120, and 150 min after the GnRH injection instead of the usual 0, 30, 60, and 90 min). The girls will also be investigated twice. In randomised order they will be given either GnRH or placebo (isotone saline), on different days. One week to one month will separate the different investigation days.

The proteinase inhibitor 4-(2-aminoethyl) benzene-sulfonyl fluoride hydrochlorid (AEBSF) will be added to some of the blood tubes, and hydrochloric acid will be added to some of the plasma. All plasma samples will be frozen and all analyses will be done at the same time. Acylated ghrelin will be analyzed by Millipore's specific ELISA kit and deacylated ghrelin will be analyzed by Cayman's specific ELISA kit.

Anthropometric data as well as pubertal state will be collected. P-glucose, S-insulin, S-follicle stimulating hormone (FSH), S-luteinizing hormone (LH), and S-estradiol will also be analyzed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Single (Participant)

入排标准

年龄范围
1 Year 至 —(Child, Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Female gender.
  • Clinical suspicion of central precocious puberty.
  • A GnRH stimulation test is to be performed to make appropriate diagnosis.

排除标准

  • Age < 1 year.
  • Weight < 10 kg.
  • Untreated hypo- or hyperthyroidism.
  • Diabetes of any kind.
  • BMI > 3 z-score.
  • Growth hormone treatment.
  • Syndrome or suspected syndrome.
  • Tumour or congenital malformation of the hypothalamus or the pituitary gland. (Neuroradiology does not have to be performed only because of the study.)
  • On going ulcus ventriculi or the patient has gone through surgery that removed part of the ventricle or changed it markedly in any other way.

研究组 & 干预措施

Gonadotropin releasing hormone (GnRH)

Active Comparator

A single intravenous injection of gonadotropin releasing hormone GnRH (Relefact LHRH 0,1 mg/mL). Dose: 100 micrograms per square meter body surface. Maximal dose: 100 micrograms.

干预措施: Gonadotropin releasing hormone (GnRH) (Drug)

Sodium chloride

Placebo Comparator

A single intravenous injection of sodium chlorid (9 mg/mL). Dose: the same volume as the volume given/to be given with GnRH, that is maximal dose = 1 mL = 9 mg sodium chlorid.

干预措施: Sodium Chloride (Drug)

结局指标

主要结局

Ghrelin concentration after GnRH injection and after saline injection

时间窗: 30-150 min after iv injections

Paired comparison will be done between the acylated ghrelin concentration after GnRH injection and the acylated ghrelin concentration after saline injection. Paired comparison will also be done between deacylated ghrelin concentration after GnRH injection and deacylated ghrelin concentration after saline injection.

次要结局

  • Deacylated ghrelin concentrations in samples treated with the inhibitor AEBSF, in samples treated with both AEBSF and hydrochloric acid, and in samples not treated with either AEBSF or hydrochloric acid(150 min after iv injections)
  • Acylated ghrelin concentrations in samples treated with and without hydrochloric acid(0-150 min after iv injections)

研究者

发起方
Region Örebro County
申办方类型
Other
责任方
Sponsor

研究点 (1)

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