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Trackers› Clinical trials› Liposomal Bupivacaine
Clinical trial register · China

Liposomal Bupivacaine Trials in China, 2026

Every study on the ClinicalTrials.gov registry that lists a site in China and is open, about to open, active-but-closed, or enrolling by invitation. Filter it, cite it, and take it away as a file.

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Source: ClinicalTrials.gov, U.S. National Library of Medicine. Complete coverage โ€” all 19052 matching records held by the registry are in this view. Synced 22 Sep 2026, 11:10 UTC
19052
Studies in scope
all four open statuses
11786
Recruiting now
open to new participants
2009
Lead sponsors
across recruiting studies
Top sites
Beijing 5
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Recruitment status
Phase
Site location
Beijing5
All 1 locations
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Liposomal Bupivacaine trials in China

5 of 19052 studies
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Status
Study
Lead sponsor
Phase
Enrol
Chinese sites
Start
Recruiting
The Efficacy and Safety of Liposomal Bupivacaine in Relieving Postoperative Pain After Laparoscopic Surgery
NCT07458256Laparoscopic Surgery, Liposomal Bupivacaine, Local Infiltration
Beijing Tiantan Hospital
Not applicable
190
Beijing
2026-03-10
Recruiting
The Efficacy and Safety of Liposomal Bupivacaine for Transversus Abdominis Plane Block in Relieving Postoperative Pain After Laparoscopic Surgery in Gynecologic Oncology
NCT07458295Laparoscopic Surgery, Gynecologic Oncology Patient, Liposomal Bupivacaine, Transversus Abdominis Plane Block
Beijing Tiantan Hospital
Not applicable
110
Beijing
2026-03-10
Recruiting
The Efficacy and Safety of Liposomal Bupivacaine for Transversus Abdominis Plane Block in Relieving Postoperative Pain After Laparoscopic Surgery
NCT07458282Laparoscopic Surgery, Liposomal Bupivacaine, Transversus Abdominis Plane Block
Beijing Tiantan Hospital
Not applicable
318
Beijing
2026-03-10
Recruiting
The Efficacy and Safety of Liposomal Bupivacaine in Relieving Postoperative Pain After Video-assisted Thoracoscopic Surgery
NCT07432711Video-assisted Thoracoscopic Surgery (VATS), Pain Management, Liposomal Bupivacaine, Local Injection
Beijing Tiantan Hospital
Not applicable
100
Beijing
2026-03-02
Recruiting
The Efficacy and Safety of Liposomal Bupivacaine for Rhomboid Intercostal Nerve Block in Relieving Postoperative Pain After Video-assisted Thoracoscopic Surgery
NCT07441902Video-assisted Thoracoscopic Surgery (VATS), Pain Management, Liposomal Bupivacaine, Rhomboid Intercostal Block
Beijing Tiantan Hospital
Not applicable
134
Beijing
2026-03-02
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Cite this view

Priya Life Science (2026). Clinical trial register: studies with a Chinese investigative site, filtered. Derived from ClinicalTrials.gov. Retrieved 27 September 2026. https://priyalifescience.com/clinical-trials-china/condition/liposomal-bupivacaine

Query this register directly
GET /api/trials?country=cn&status=recruiting&format=json Try it now →

About this register

This register is built from ClinicalTrials.gov, the trial registry run by the U.S. National Library of Medicine. It includes every study on the registry that lists at least one investigative site in China and is recruiting, not yet recruiting, active but no longer recruiting, or enrolling by invitation: 19,052 studies in total at the last sync on 22 Sep 2026, 11:10 UTC. The full list can be downloaded as CSV or queried as JSON through the register API.

This page shows the 5 of those studies listing the condition Liposomal Bupivacaine that also match the filters currently applied.

How many Liposomal Bupivacaine trials are recruiting in China?

5 of the 5 studies on this page are recruiting new participants as of the 22 Sep 2026, 11:10 UTC sync. A further 0 have not yet opened recruitment, 0 are active but closed to new participants, and 0 are enrolling by invitation only. Eligibility for any study is decided by its study team.

Summary by phase

Studies by phase (Liposomal Bupivacaine), 5 studies
PhaseStudiesRecruitingShare
Not applicable55100%

Most active sponsors

Lead sponsors with the most studies (Liposomal Bupivacaine)
Lead sponsorStudiesRecruiting
Beijing Tiantan Hospital55
Listing here is informational and not medical advice; eligibility is determined by each study team. See also the Ireland, UK, EU, USA and India registers.