A Study of Intramuscular Sebacoyl Dinalbuphine Ester for Post-Hemorrhoidectomy Pain Management
A Randomized, Double Blind, Placebo-Controlled, Single Dose Study to Assess The Safety and Efficacy of Intramuscular Sebacoyl Dinalbuphine Ester (SDE) for Post-Hemorrhoidectomy Pain Management
Sponsor: Lumosa Therapeutics Co., Ltd.
A PHASE2/PHASE3 clinical study on Analgesia Disorder and Pain, this trial is completed. The trial is conducted by Lumosa Therapeutics Co., Ltd. and has accumulated 8 data snapshots since 2012. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Status Flow
Change History
8 versions recorded-
Feb 2026 — Present [monthly]
Completed PHASE2/PHASE3
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Sep 2025 — Feb 2026 [monthly]
Completed PHASE2/PHASE3
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Sep 2024 — Sep 2025 [monthly]
Completed PHASE2/PHASE3
-
Jul 2024 — Sep 2024 [monthly]
Completed PHASE2/PHASE3
Phase: PHASE2_PHASE3 → PHASE2/PHASE3
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Jan 2021 — Jul 2024 [monthly]
Completed PHASE2_PHASE3
▶ Show 3 earlier versions
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Jun 2018 — Jan 2021 [monthly]
Completed PHASE2_PHASE3
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Feb 2017 — Jun 2018 [monthly]
Completed PHASE2_PHASE3
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Jan 2017 — Feb 2017 [monthly]
Completed PHASE2_PHASE3
First recorded
Dec 2012
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Lumosa Therapeutics Co., Ltd.
For direct contact, visit the study record on ClinicalTrials.gov .