WHO ICTRP trial
Genetics and clinical profile of patients with 11-Beta hydroxylase deficiency
CTRI/2019/10/021495 · Clinical Trials Registry India (CTRI) · Not Recruiting
Key facts
| Trial ID | CTRI/2019/10/021495 |
|---|---|
| Public title | Genetics and clinical profile of patients with 11-Beta hydroxylase deficiency |
| Scientific title | Clinical, Biochemical and Genetic profile of Patients with Congenital Adrenal Hyperplasia due to 11-βHydroxlase deficiency. |
| Registry | Clinical Trials Registry India (CTRI) |
| Recruitment status | Not Recruiting |
| Study type | Observational |
| Countries | India |
| Conditions | Health Condition 1: E250- Congenital adrenogenital disordersassociated with enzyme deficiency |
| Interventions | Intervention1: NIL: NIL Control Intervention1: NIL: NIL |
| Registration date | Jan 10, 2019 |
| Target size | 20 |
| Secondary IDs | Not applicable |
| Registry page | ctri.nic.in |
At a glance
- No Results available
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: