Opioid-free anesthesia monitored by analgesia nociceptive index for hepatectomy in cirrhotic

Opioid-free anesthesia monitored by analgesia nociceptive index for cirrhotic patients undergoing hepatic focal lesion resection

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

PACTR

Registry ID

PACTR202301766708922

Enrollment

Registered

2023-01-16

Start date

2022-12-01

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

Anaesthesia

Interventions

opioid free anesthesia group

opioid based anasthesia

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: cirrhotic patients candidate for hepatic resection with Child classification (A)

Exclusion criteria

Exclusion criteria: 1-patients suffered from Major intraoperative events (e.g. severe hemodynamic instability, massive blood loss, massive blood products transfusion). 2-Allergic patients to any of the study drugs. 3- Opioid addiction. 4-Body-mass index higher than 40 kg/m². 5-unwilling to participate in the study.

Design outcomes

Primary

Measure	Time frame
investigate the analgesic effect of OFA in cirrhotic patients scheduled for hepatic focal resection compared to opioid based anesthesia by Analgesia Nociception Index	—

Secondary

Measure	Time frame
hemodynamic effects	—

Countries

Egypt

Contacts

Public Contacthanaa rashed

anasthesia lecturer

hanaarashed2020@yahoo.com01002345678

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026