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NCT Number: NCT06110910

Long-term Efficacy and Safety Evaluation of Growth Hormone in Children in China(CGLS)

Short stature is a relatively common pediatric condition, referring to individuals whose height is more than 2 (-2 SD) standard deviations below the average height of a similar age, gender, and ethnicity population in similar living conditions, or those below the third percentile (-1.88 SD). This study is an open-label, multicenter, prospective and retrospective, observational, cohort study aimed at assessing the long-term safety and efficacy of PEG-rhGH or rhGH treatment for Chinese children with short stature. The study is divided into retrospective cohorts, retrospective prospective cohorts, and prospective cohorts. It is expected to include approximately 10000 patients (including around 3000 in the retrospective cohorts and around 7000 in the retrospective prospective and prospective cohorts). The total duration is expected to be 16 years, including 2 years for study center initiation and patient recruitment and follow-up of patients in the retrospective prospective and prospective cohorts until near-adult height (NAH). The primary objective is to evaluate the long-term safety of PEG-rhGH or rhGH for the treatment of children with short stature (including GHD, ISS, SGA, TS, PWS, NS, SHOX gene deletion, and other etiologies); the secondary objective is to assess the effectiveness of PEG-rhGH or rhGH treatment for children with short stature (including GHD, ISS, SGA, TS, PWS, NS, SHOX gene deletion, and other etiologies).

Recruiting

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Key information

Age range

2 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

TongjiHospital

Wuhan, Hubei, 430030, China

Location status: Recruiting

Location contact

xiaoping Luo, doctor

CONTACT

[email protected]

13387522645 ext. 86

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children aged 2 years and older with various causes of short stature.
  • Height below the 3rd percentile (-1.88 SD) compared to the height of normal, healthy children of the same age and gender.
  • Belonging to one of the following indications: GHD, ISS, SGA, TS, PWS, NS, SHOX gene deletion, or other causes of short stature.

Note: In this study, the inclusion criteria for the PWS cohort do not impose restrictions on height and age at the start of treatment.

Exclusion criteria

  • Patients with fully closed growth plates.
  • Patients with signs of potential tumor progression or those already diagnosed with tumors.
  • Allergic reactions to growth hormone or its adjuvants.
  • Patients who have received any growth hormone treatment other than the investigational drug in the six months prior to screening.
  • Any other circumstances deemed unsuitable for study inclusion by the investigator.

Treatment and study plan

Polvethylene glycol recombinant human growth hormone injection (PEG-rhGH) or recombinanthuman growth hormone injection (rhGH)

Drug

Polvethylene glycol recombinant human growth hormone injection (PEG-rhGH) and recombinanthuman growth hormone injection (rhGH) were used.

Other names: PEG-rhGH or rhGH

Primary outcomes

  1. The AE (Adverse Event) and SAE (Serious Adverse Event) occurrence rates

    Time frame: From the time of signing the informed consent form to the near adult height(NAH), the overall assessment time was approximately 192 months.

    An adverse event refers to any unfavorable medical occurrence in a patient after receiving the investigational drug, which can manifest as symptoms, signs, diseases, or abnormalities in laboratory tests, but may not necessarily be causally related to the investigational drug. SAE, on the other hand, stands for serious adverse events, which encompass events such as patient death, life-threatening situations, permanent or severe disabilities or functional loss, hospitalization or extended hospital stays, as well as congenital anomalies or birth defects, among other adverse medical occurrences, following the administration of the investigational drug.

Study contacts

Contact information is provided by the study sponsor or research team.

xiaoping Luo, doctor

CONTACT

[email protected]

13387522645 ext. 86

Sponsors and collaborators

Lead sponsor

Xiaoping Luo

Other

Registry information

Official study title

Long-term Efficacy and Safety Evaluation of Growth Hormone in Children in China(CGLS)-an Open-label, Multicenter, Prospective and Retrospective Observational Study

Important dates

Study start
2023
Primary completion
2027
Study completion
2027
First posted
Nov 1, 2023
Registry last updated
Nov 5, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.