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Precocious Puberty Clinical Trials

A listing of Precocious Puberty medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.

RESULTS

Found (12) clinical trials

Leuprorelin Acetate DPS (Leuplin DPS) Treatment Quarterly in Patients With Central Precocious Puberty

A multicenter, open-label, prospective study to evaluate the safety and efficacy of leuprorelin acetate DPS (Leuplin DPS) treatment quarterly in patients with central precocious puberty

Phase

The Genetic Investigation of Reproductive Disorders (Including Kallmann Syndrome)

The World Health Organization estimates approximately 10% of couples experience some sort of infertility problem. In humans, puberty is the process through which we develop reproductive capacity. Disorders of puberty have provided insight into the biology of reproduction and genetic technologies have enabled us to deepen understanding in this field. ...

Phase N/A

Analysis of Body Mass Index in Central Precocious Puberty Patients Treated With Leuprolide Acetate

Analysis of body mass index in Central Precocious Puberty patients treated with leuprolide acetate

Phase

Clinical Trial of Experienced Chinese Herbal Formulas on Different Types of Precocious Puberty

In the research, 138 precocious puberty children are randomly divided into the Ziyinxiehuo granules group (69 cases) and Zishenqinggan granules group(69 cases). Patients in Ziyinxiehuo granules group are treated with a series of experienced chinese herbal formulas, whereas the Zishenqinggan granules group received with different series of experienced chinese herbal ...

Phase N/A

Pharmacokinetic Study of Leuprolide Acetate Injectable Suspension in the Treatment of Central Precocious Puberty

Primary Objectives Determine the effectiveness of leuprolide acetate 45 mg for injectable suspension for treatment of children with CPP. Secondary Objectives - Evaluate the safety and tolerability of leuprolide acetate 45 mg for injectable suspension in children with CPP - Characterize the burst kinetics of leuprolide acetate 45 mg after ...

Phase

Analysis of Genetic and Environmental Parameters Influencing Growth Rate of Precocious Puberty Children

The goal of CPP-EDG 01 study is to assess possible genetic and/or environmental parameters which may influence the growth rate of children affected by precocious puberty. In this view, we are collecting clinical data and biological samples of children attended as outpatients at the Pediatric Endocrine Center of Pisa from ...

Phase

Histamine Responsiveness in McCune-Albright Syndrome

Objectives of this study are to determine if: 1. Patients with McCune-Albright syndrome differ from unaffected controls in wheal and flare response to histamine and codeine. 2. Affected skin will differ from unaffected skin in wheal and flare response to histamine and codeine. 3. IgE and IL-4 levels in MAS ...

Phase N/A

Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders

Overview Our work is divided into two main areas of investigation: the discovery of new, yet-undiscovered genes for conditions of early (i.e. precocious) puberty, delayed puberty, and/or absence of pubertal development (i.e. Kallmann syndrome/hypogonadotropic hypogonadism). Identification of new genes requires either a single large family or a collection of smaller ...

Phase N/A

Screening and Natural History of Patients With Polyostotic Fibrous Dysplasia and McCune-Albright Syndrome

Polyostotic fibrous dysplasia (PFD) is a sporadic disorder which affects multiple sites in the skeleton. The bone at these sites is rapidly resorbed and replaced by abnormal fibrous tissue or mechanically abnormal bone. PFD may occur alone or as part of the McCune-Albright Syndrome (MAS), a syndrome originally defined by ...

Phase N/A

The Effect of Decaffeinated Green Tea Polyphenol Intake on the Risk of Precocious Puberty Among Obese Girls

Simple obese girls are prone to premature or early puberty. The topic proposed based on previous studies, recruiting of 200 simple obesity girls, aged 7 to 10 years old. After the informed consent, they will be randomly divided into intervention group and control group, intervention group will be given tea ...

Phase N/A