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Study identifier: NCT06732427 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Clinical Study of Fospropofol Disodium for Injection in the Painless Endoscopic Diagnosis and Treatment

Condition: Efficacy and Safety  ·  Sponsor: Affiliated Hospital of Nantong University

PhaseNA
Planned participants426
Who can joinAll sexes, 50 Years to 65 Years
Healthy volunteersNo

About this study

This is a study on the efficacy and safety of fospropofol disodium for injection in painless endoscopic diagnosis and treatment, project No.2024-YCRF-M1021, which will take more than 2 years to complete. This is a multicenter, randomized, double-blind, controlled clinical study. Using a computer-generated randomized number table, the patients were divided into two groups: the group L (fospropofol disodium group) and the group B (propofol group). After determining the group of enrolled patients, the drug was administered by two fixed anesthesiologists By participating in this study, it is possible to make your anesthesia induction stable, stable intraoperative circulation, awake and safe and comfortable, to reduce the incidence of intraoperative hypoxemia, intraoperative awareness, cardiovascular and cerebrovascular malignant events (malignant arrhythmia, cardiac arrest), which is conducive to your rapid postoperative recovery and reduce hospitalization costs.

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

Talk to the study team

Gao YT Director of Department of Anesthesiology, Master  ·  +86 13962988003  ·  gyt19700114@sina.com

Liu YF project implementation PI, Master  ·  +86 13506289927  ·  winters_cool@126.com

Always discuss trial participation with your own doctor first.

Locations (5)

Hai 'an People's HospitalHai’an, Jiangsu, ChinaRecruiting
Affiliated Hospital of Nantong UniversityNantong, Jiangsu, ChinaRecruiting
Qidong People's HospitalQidong, Jiangsu, ChinaNot Yet Recruiting
Rudong County Hospital of Traditional Chinese MedicineRudong, Jiangsu, ChinaRecruiting
Rugao People's HospitalRugao, Jiangsu, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06732427