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Clonidine treatment for short stature
Lancet (London, England)
|May 30, 1987
Summary
Clonidine treatment effectively increased height velocity in children with constitutional growth delay (CGD). A significant growth response was observed, with sustained effects in some children even after treatment cessation, indicating potential therapeutic value.
Area of Science:
- Pediatric Endocrinology
- Pharmacology
Background:
- Constitutional growth delay (CGD) is a common condition in children.
- Effective therapeutic interventions for CGD are continuously sought.
Purpose of the Study:
- To evaluate the efficacy of oral clonidine in stimulating linear growth in children with CGD.
- To identify predictors of treatment response and assess the duration of clonidine's effect.
Main Methods:
- A study involving 34 pubertal children diagnosed with CGD.
- Oral administration of clonidine twice daily.
- Monitoring of height velocity changes over 12 months, with subsequent withdrawal and reintroduction phases.
Main Results:
- Increased height velocity was observed in 25 out of 34 children during clonidine treatment.
- A mean growth increment of 4.4 cm/yr was noted in the first 6 months.
- Sustained growth increments were observed in 13 of 22 children after 12 months of treatment.
- A high height standard deviation score and low baseline growth velocity predicted a better response.
Conclusions:
- Oral clonidine is a potentially effective therapy for enhancing linear growth in children with CGD.
- The drug demonstrated a good safety profile with no noticeable side-effects.
- Predictive factors for treatment response were identified, aiding in patient selection.