WHO ICTRP trial
A Comparative Study of Tegileridine Fumarate versus Sufentanil for Postoperative…
ChiCTR2500113605 · Chinese Clinical Trial Registry (ChiCTR) · Not Recruiting
Key facts
| Trial ID | ChiCTR2500113605 |
|---|---|
| Public title | A Comparative Study of Tegileridine Fumarate versus Sufentanil for Postoperative Analgesia Following Laparoscopic Total Hysterectomy: A Prospective, Randomized, Double-Blind, Controlled Clinical Trial Focusing on Quality of Recovery as the Primary Endpoint. |
| Scientific title | A Comparative Study of Tegileridine Fumarate versus Sufentanil for Postoperative Analgesia Following Laparoscopic Total Hysterectomy: A Prospective, Randomized, Double-Blind, Controlled Clinical Trial Focusing on Quality of Recovery as the Primary Endpoint. |
| Primary sponsor | Liaocheng Second People's Hospital |
| Registry | Chinese Clinical Trial Registry (ChiCTR) |
| Recruitment status | Not Recruiting |
| Study type | Interventional study |
| Countries | China |
| Conditions | Gynecological uterine diseases |
| Interventions | Experimental group:Postoperative analgesia: Tigillitin fumarate is prepared at 0.05mg/ml;Control group:Postoperative analgesia: Sufentanil is prepared at 5ug/ml |
| Registration date | Dec 1, 2025 |
| Target size | Experimental group:60;Control group:60 |
| Registry page | chictr.org.cn |
At a glance
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: