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Ultrasound-guided Continuous Low Serratus Anterior Plane Block in Hepatocellular Carcinoma Surgery

The Role of Continuous Low Serratus Anterior Plane Block in Hepatocellular Carcinoma Surgery: a Randomised Clinical Trial.

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05531864
Acronym
RCT
Enrollment
160
Registered
2022-09-08
Start date
2021-01-01
Completion date
2024-02-29
Last updated
2024-02-28

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

Conditions

Liver Neoplasms, Postoperative Analgesia, Serratus Anterior Plane Block

Keywords

serratus anterior plane block, Postoperative analgesia, liver cancer

Brief summary

To investigate the clinical application of ultrasound-guided continuous low serratus anterior plane block in open surgery for hepatocellular carcinoma.

Detailed description

METHODS: Patients with hepatocellular carcinoma who attended our hospital from January 2021 to April 2023 were divided into CS group and N group according to the random number table method; CS group underwent ultrasound-guided continuous low anterior serratus plane block and N group underwent ultrasound-guided single anterior serratus plane block combined with rectus abdominis sheath block; the operation time, anesthesia time, incision length, sensory block time and sensory block maintenance time were counted and recorded. Pain score (NRS) was used to detect analgesia; alanine aminotransferase (ALT), liver function aspartate aminotransferase (AST), and prothrombin time (The time of thrombin, NRS) were measured by fluorescent quantitative PCR. (The time of thrombin (APTT), total bilirubin (TBIL) levels and adverse reactions.

Interventions

PROCEDUREUltrasound-guided continuous low serratus anterior plane block

Low anterior serratus plane block, move the mid-axillary line 4 and 5 intercostal puncture points are moved down and the puncture is changed to 7 and 8 intercostal.

PROCEDUREUltrasound-guided single serratus anterior plane block

Ultrasound-guided single anterior saw plane block was performed, and a needle was injected between the 4th and 5th costals in the midaxillary line.

Sponsors

Liu Di
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Age 18-60 years; 2. ASAI-II; 3. BMI: 18-29 kg/m2

Exclusion criteria

1. Combined cardiac, cerebral, hepatic, and renal failure; 2. Comorbid psychiatric and neuromuscular disorders; 3. A history of allergy to anesthetic drugs; 4. Participation in other recent clinical or drug trials.

Design outcomes

Primary

MeasureTime frameDescription
Block plane30 minute after the surgery beginsThe effect of anesthesia after ultrasound-guided nerve block was measured using planimetry, as well as the area being anesthetized. The chest wall between T2-T9 and ice cotton balls was used to assess the extent and extent of anesthesia block.
visual analogue scale24 hours after surgeryThe visual analogue scale (VAS) of the patient's pain was recorded 24 hours after operation.

Secondary

MeasureTime frameDescription
Patient satisfaction48 hours after surgery.The patient's satisfaction with the analgesia 2 days after surgery was recorded. The analgesic effect: 1-3 as satisfactory, 4-6 as unsatisfactory, 7-10 as ineffective
Remedial analgesic drug24 hours after surgery.Whether other analgesic drugs were added within 24 hours after operation was recorded
Intraoperative blood pressure changes2 hours after the beginning of surgery.Blood pressure changes were measured directly by radial artery puncture and recorded. The changes in blood pressure and heart rate before and after excision and the use of intraoperative opioids.
Intraoperative heart rate changes2 hours after the beginning of surgery.The curve of the change of the operative heart rate was recorded through the anesthesia machine.

Countries

China

Contacts

Primary ContactJiang Fei
1277636690@qq.com18283236053

Outcome results

None listed

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