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Study identifier: NCT06078969 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Oral Prednisone in Treating LCH of Bone in Childhood and Adolescence

Condition: Langerhans Cell Histiocytosis of Bone  ·  Sponsor: Shanghai Changzheng Hospital

PhasePhase 2
Planned participants118
Who can joinAll sexes, 2 Years to 17 Years
Healthy volunteersNo

About this study

Langerhans cell histiocytosis (LCH) of bone is a benign-tumor-like osteolytic lesion in childhood and adolescence, which is characterized by the aberrant activation of antigen presenting cells. Rather than the multi-system involvements of LCH, no standard or widely-accepted therapeutic regimens were established for LCH of bone. In the previous clinical practice, several LCH patients obtained remarkable pain relief after taking prednisone. Therefore, the investigators aim to conducting a multi-center, open-labelled, randomized-controlled, Phase II study to investigate the efficacy and safety of oral prednisone in treating LCH of bone in children and adolescents. The enrolled patients will be randomly recruited to the following groups: (1) Oral prednisone \[Test group); (2) Regular observation \[Control group\].

This description comes directly from the study's public registry record.

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Locations (1)

Shanghai Changzheng HospitalShanghai, Shanghai Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06078969