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Retrospective analysis of factors related to height impairment in classic 21-hydroxylase deficiency patients aged 0-3 years

Retrospective analysis of factors related to height impairment in classic 21-hydroxylase deficiency patients aged 0-3 years

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100055063
Enrollment
Unknown
Registered
2021-12-31
Start date
2022-01-01
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

21-hydroxylase deficiency

Interventions

case series:None

Sponsors

Shenzhen Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 3 Years

Inclusion criteria

Inclusion criteria: 1. Children with 21-OHD who have been diagnosed by genetics before 2021-12-31; 2. The karyotype is consistent with the rearing sex; 3. After the diagnosis, they all received regular glucocorticoid therapy (limited to hydrocortisone acetate tablets ± 9a-fluorocortisone), and the dose is not limited; 4. Regular follow-up, with inspection and medication (follow-up time requirements: =37 weeks and <42 weeks), birth weight (2500-4000g), and the mother did not receive hormone therapy during pregnancy; 7. Taking the height and bone age of the child at 3 years old as the end point, the end point can be reached.

Exclusion criteria

Exclusion criteria: 1. Suffering from diseases or other chronic diseases that affect physical growth; 2. Long-term use of other drugs or the use of growth hormone, gonadotropin-releasing hormone analogs, aromatase inhibitors, androgen blockers, inhaled/topical hormone-containing drugs or a combination of the above drugs; 3. Lack of relevant birth history, children with familial short stature or unable to provide family history; 4. Infants and young children with central precocious puberty, or those who mistakenly take estrogen drugs or use hormone drugs or take supplements/Chinese herbal medicine soup during infancy and young children become peripheral precocious puberty; 5. Psychomotor retardation.

Design outcomes

Primary

MeasureTime frame
Serum steroid hormones level;

Secondary

MeasureTime frame
Bone age;Drug dosage;

Countries

China

Contacts

Public ContactLiang Liyang

Sun Yat-sen Memorial Hospital, Sun Yat-sen University

liangliy@mail.sysu.edu.cn+86 13688891219

Outcome results

None listed

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