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Intertransverse Process Block for Quality of Recovery Post-Open Hepatectomy

Effect of Intertransverse Process Block on the Quality of Recovery Post-Open Hepatectomy: A Pilot Non-Randomised Study of Intervention

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06957041
Acronym
ITPB QoR
Enrollment
20
Registered
2025-05-04
Start date
2025-05-01
Completion date
2026-10-01
Last updated
2025-05-04

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

Conditions

Hepatectomy, Intertransverse Process Block, Quality of Recovery (QoR-15)

Brief summary

The study aims to assess the analgesic efficacy of the ITPB at the retro-SCTL space in patients undergoing major open hepatectomy surgery. This is assessed by: Primary Objective: Primary outcome measure: ● Assessing the quality of recovery 15 (QoR15) score at 24 and 48 hours Secondary outcome measure: * Number of anaesthetic and hypoesthetic dermatomes on the ventral and dorsal aspect of the thorax on both the sides at 30 minutes of block completion and during the post anaesthetic room (PACU) discharge * Assessing the 24-hour area under the curve of postoperative pain numerical rating score (NRS, 0-10) at rest and deep breathing or upon use of triflow. * Assessing the amount of postoperative morphine (mg) equivalent consumption at 24 and 48 hours * Time to discharge from High dependency unit (HDU) or Intensive care unit (ICU) Hypothesis: The investigators hypothesize that the application of ITPB targeting the retro-SCTL space in patients undergoing open hepatectomy will improve overall quality of recovery and pain score.

Interventions

The patient(s) will receive a pre-induction Intertransverse process block as pilot study

Sponsors

Chinese University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

\- Adult patients aged 18-75 years of ASA I - III physical status classification undergoing open hepatectomy for benign or malignant liver lesion.

Exclusion criteria

* Patient refusal * Patients who are unable to comprehend the QoR15 form * Local or systemic infection * Coagulopathy leading to absolute contraindication to regional anesthesia * Contraindication to local anaesthetics (LA) such as LA allergy

Design outcomes

Primary

MeasureTime frameDescription
Quality of Recovery (QOR-15)24 and 48 hoursThe QoR-15 scale is a global measure of postoperative recovery, with a score ranging from 0 (extremely poor QoR) to 150 (excellent QoR). The QoR-15 has since become the most widely reported measure of patient-assessed QoR after surgery. QoR-15 has no units.

Secondary

MeasureTime frameDescription
Dermatomal blockade on Thorax 30 minutes upon block completionUp to 30 minutes after block completionTo assess the number of anaesthetic and hypoesthetic dermatomes on the ventral and dorsal aspect of the thorax on both the sides at 30 minutes of block completion and during the post anaesthetic room (PACU) discharge. This will be done by ice block test. The blockade is considered positive if patient has a reduction in cold sensation over the tested dermatome compared to non-blocked areas such as forehead.
24 hours area under curve of postoperative pain scoreUp to 24 hoursAssessing the 24-hour area under the curve of postoperative pain numerical rating score (NRS, 0-10) at rest and deep breathing or upon use of triflow.
Morphine consumption at 24 and 48 hours postoperativelyAt 24 and 48 hours postoperativelyAssessing the amount of postoperative morphine (mg) equivalent consumption at 24 and 48 hours
Time to discharge from HDU / ICUUp to 5 daysTime to discharge from High dependency unit (HDU) or Intensive care unit (ICU) up to 5 days

Contacts

Primary ContactWing Sum Li, MBChB, BA
vickiliwingsum@gmail.com852-55699340

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026