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The Effect of Recombinant Human Growth Hormone on Refractive Status in Prepubertal Children with Short Stature

The Effect of Recombinant Human Growth Hormone on Refractive Status in Prepubertal Children with Short Stature

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100680
Enrollment
Unknown
Registered
2025-04-14
Start date
2025-07-22
Completion date
Unknown
Last updated
2025-09-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myopia

Interventions

Short-acting observation group:None
Control group:None
Long-term observation group:None

Sponsors

Wenzhou Medical University Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Age >=6 years old and =-3.00D, and astigmatism (cylindrical lens) is 0.00 to -1.50D, and anisometric refraction in both eyes =5.0; 6. Intraocular pressure: 10-21mmHg, intraocular pressure difference in both eyes<=5mmHg; 7. No history of ocular organic disease and ocular surgery; 8. Have not used myopia prevention and control methods (such as low-concentration atropine, red light therapy device, orthokeratology lenses, etc.) in the past; 9. No systemic diseases, other endocrine diseases, chromosomal abnormalities and no organic diseases; 10. No previous history of growth hormone therapy; 11. The patient's parent or legal guardian must read, understand and sign the informed consent form, and the patient with reading ability must read (or be read to them by someone else) and sign the informed consent form for the child.

Exclusion criteria

Exclusion criteria: 1. Children with a history of rhGH allergy or systemic diseases, endocrine diseases, or chromosomal abnormalities; 2. Use of drugs such as glucocorticoids that may interfere with the action of growth hormone in the past 3 months; 3. Congenital skeletal abnormalities, lameness or scoliosis; 4. Eye diseases such as glaucoma, cataracts, fundus lesions, active ocular inflammation, etc.; 5. Have strabismus, amblyopia and other eye diseases; 6. History of ocular trauma, ocular surgery, or serious ocular infection; 7. Those who use any myopia prevention and control measures during treatment, such as using low-concentration atropine eye drops or prevention and control lenses or devices; 8. Expected treatment time is less than 12 months and other conditions that the investigator believes are not suitable for inclusion in this clinical trial; 9 Inability to sign informed consent.

Design outcomes

Primary

MeasureTime frame
Axial length;Objective refractive diopter after ciliary muscle paralysis;

Secondary

MeasureTime frame
Choroid;Subjective refraction refractive power;Best corrected visual acuity;

Countries

China

Contacts

Public ContactXinjie Mao

Wenzhou Medical University Eye Hospital

mxj@mail.eye.ac.cn+86 137 0588 0472

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026