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Anrikefon Combined with Thoracic Paravertebral Block for Multimodal Analgesia in Thoracoscopic Esophagectomy: A Prospective Cohort Study

Anrikefon Combined with Thoracic Paravertebral Block for Multimodal Analgesia in Thoracoscopic Esophagectomy: A Prospective Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111526
Enrollment
Unknown
Registered
2025-11-01
Start date
2025-11-01
Completion date
Unknown
Last updated
2025-11-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esophageal cancer

Interventions

A1 group:Postoperative PCIA anrikefon 0.3µg/kg
A2 group:Postoperative PCIA anrikefon 0.6µg/kg

Sponsors

Anhui Provincial Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: Age: 65 years old to 80 years old, gender not limited. 2.ASA classification: Grade II - III. 3.BMI: 18-30 kg/m^2. 4. Expected moderate to severe postoperative pain (NRS>=4). 5. The patient or their family members can understand the research content, voluntarily sign the informed consent form, and are willing to abide by the requirements of the trial protocol.

Exclusion criteria

Exclusion criteria: 1.Those who are allergic to or contraindicated to benzodiazepines, opioids, cyclopofol, flumaciclib, naloxone, amreliphine and their drug components. 2. Patients with severe heart, lung or kidney insufficiency, combined with multiple chronic diseases, who cannot tolerate surgical anesthesia. 3. Those with a history of alcohol abuse, opioid allergy or abuse of such drugs. 4. Other circumstances that the researcher deems unsuitable for enrollment. 5. Patients who have had neurological diseases or undergone surgery recently.

Design outcomes

Primary

MeasureTime frame
Difference in resting/motor pain intensity within 24 hours after surgery;

Secondary

MeasureTime frame
First time to remedy analgesia;Total opioid consumption;Postoperative recovery indicators;Security indicators;

Countries

China

Contacts

Public ContactChaoliang Tang

Anhui Provincial Cancer Hospital

chaolt@ustc.edu.cn+86 138 6677 7142

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026