Autopsy report · NCT07325903
Research of Integrated Traditional Chinese and Western Medicine on Precocious Puberty
Cause of deathSlow enrollment
“The study was terminated prematurely due to the inapplicability of the primary outcome measure”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Early Phase 1
- Sponsor
- Children's Hospital of Fudan University
- Sponsor type
- University, hospital or other
- Conditions
- Puberty, Precocious
- Interventions
- administered "Mulberry and Lotus Leaf Heat-Clearing Granules," with the following drug composition: mulberry leaves, lotus leaves, fresh rehmannia, anemarrhena, scutellaria, atractylodes, etc.; 10% drug-containing placebo, for a period of 3 months.
- Participants
- 0
- Sites
- 1
- Countries
- China
Trials that died the same way
- PFC Sigma Fixed and Mobile Knee Study
“The study was terminated at the point the primary endpoint and early milestones were reached and because long term outcomes were available from other sources” - Leronlimab (PRO 140) Combined With Carboplatin in Patients With Cytokine Chemokine Receptor 5 Positive (CCR5+) mTNBC
“Study terminated prematurely due to business reasons. Participants are no longer examined or receiving intervention.” - Prevention of NAFLD in Hispanic Children
“Study was terminated due to a lack of funding. Data collection was completed for 12-month outcomes; however, funding limitations prevented follow-up for longer timeframes, and some outcomes were not fully collected.” - Avelumab in Previously Untreated Patients With Epithelial Ovarian Cancer (JAVELIN OVARIAN 100)
“The study was terminated based on the results of a planned interim analysis that showed futility of efficacy.” - Anti-NY ESO-1 mTCR Peripheral Blood Lymphocytes
“Due to lack of accrual the study was formally terminated on 01-JUL-2020. Primary Completion and Study Completion Dates have been revised based accordingly based on respective definitions”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.