perioperative Analgesic Effect of Erector Spinae Plane Blocks in Whipple Surgery.

Evaluation of perioperative Analgesic Effect of Erector Spinae Plane Blocks in Whipple Surgery :a Randomized Controlled Study

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

PACTR

Registry ID

PACTR202306801227223

Enrollment

Registered

2023-06-26

Start date

2023-03-01

Completion date

Unknown

Last updated

2026-01-27

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

Conditions

Anaesthesia

Interventions

erector spinae block

thoracic epidural

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: - Patients aged 18 to 65 years of both sexes candidate for Whipple operation and classified by American Society of Anesthesiologists (ASA) II and III with Body-mass index of less than 40 kg/m².

Exclusion criteria

Exclusion criteria: - Pre-existing signi?cant cardiac dysfunction, respiratory, renal or cerebrovascular diseases. - Patients allergic to any of the study drugs, with opioid addiction or alcohol abuse. - Body-mass index higher than 40 kg/m². - Contraindications for neuroaxial block (e.g. Coagulopathy). - Patients unwilling to participate in the study

Design outcomes

Primary

Measure	Time frame
To study the impact of ESP Block on hemodynamic stability and maintenance of intra-operative Analgesia Nociception Index (ANI) accepted range.	—

Secondary

Measure	Time frame
To evaluate the postoperative pain by visual analogue score (VAS), total opioid requirements and incidence of post-operative complications (as measured by the comprehensive complication index (CCI)) within 48 hours.	—

Countries

Egypt

Contacts

Public Contacthanaa rashed

lecturer of anasthesia

hanaarashed2020@yahoo.com0248986754

Outcome results

None listed

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